Xin-An Zhang
Hui Kong- College of Exercise and Health, Shenyang Sport University, Shenyang, China
Osteoarthritis (OA) is a common disabling disease which has a high incidence rate in the elderly. Studies have found that many factors are involved in the pathogenesis of OA. Hypoxia-inducible factors (HIFs) are core regulators that induce hypoxia genes, repair the cellular oxygen environment, and play an important role in the treatment of OA. For example, HIF-1α can maintain the stability of the articular cartilage matrix, HIF-2α is able to cause chondrocyte apoptosis and intensify in-flammatory response, and HIF-3α may be the target gene of HIF-1α and HIF-2α, thereby playing a negative regulatory role. This review examines the mechanism of HIFs in cartilage extracellular matrix degradation, apoptosis, inflammatory reaction, autophagy and then further expounds on the roles of HIFs in OA, consequently providing theoretical support for the pathogenesis of OA and a new target for OA treatment.
1 Introduction
Osteoarthritis (OA) is a common disabling disease that occurs most frequently in the elderly (1). With the growth of the aging population in China, the incidence of OA has showed a rising trend (2). The occurrence of OA is associated with many causes and may be linked to age, gender, obesity, trauma, infection, and other factors (3). OA is a chronic disease, with mild joint swelling and pain in its early stage. With the progression of the disease, the pain becomes increasingly severe, and apparent joint swelling, deformity, and stiffness occur in the late stage (4). In recent years, many studies have confirmed that hypoxia-inducible factors (HIFs) play a vital role in regulating articular cartilage hypoxia; moreover, HIFs are closely related to the progression of OA (5).
HIFs are core regulatory factors that induce hypoxia genes and repair the cellular oxygen environment. HIFs are heterogeneous protein dimers formed by the polymerization of two different subunits: the α and β subunits (6). HIF-1α, HIF-2α, and HIF-3α are three members of the human HIF-α protein family. They are hardly expressed under normal oxygen conditions, but their expressions are significantly up-regulated under hypoxic stress. Under normal oxygen conditions, HIF-1α is rapidly degraded. However, under hypoxia, the HIF-1α degradation is inhibited, its content will increase, and it will enter the nucleus and combine with the corresponding subunits to form an active HIF-1α transcription factor. HIF-1α is mainly involved in regulating autophagy and apoptosis, promoting chondrocyte phenotypes, and maintaining the vitality of chondrocytes (7). In addition, HIF-1α also plays a biphasic role in regulating inflammatory response by regulating VEGF and EPO, and finally promotes chondrocytes to adapt to a hypoxic environment (8). On the contrary, HIF-2α is mainly involved in inducing the expression of catabolic factors in chondrocytes, enhancing the expression of Fas, promoting the apoptosis of chondrocytes, and intensifying the inflammatory reaction, thus leading to the destruction of articular cartilage (9). The functions of HIF-1 α and HIF-2 α are different. Numerous abnormal transformations from HIF-1α to HIF-2α may be one of the mechanisms of OA (10). A moderate reduction in oxygen partial pressure can induce the synthesis of HIF-3α mRNA, and the HIF-3α mRNA level increases with the duration of systemic hypoxia, which appears in many organs, such as lung, kidney and cerebral cortex. The hypoxic induction of HIF-3a depends on HIF-pathway, such as HIF-1 α and HIF-2 α. HIF-3α may be the target gene of HIF-1α and HIF-2α (11, 12). In addition, some transcription factors, such as NFjB, are also involved in the regulation of HIF-3α. NFjB is a transcription factor that is often involved in hypoxia-driven signaling and plays an important role in the regulation of HIF-3α, the inhibition of HIF-3a under hypoxia could be a secondary effect of NFjB inhibition (13).
This review discusses the mechanism of HIFs in the extracellular matrix (ECM) degradation of articular cartilage, apoptosis, inflammatory reaction, and autophagy and then expounds on the roles of HIFs in OA, thereby providing theoretical support for the pathogenesis of OA and identifying a new target for OA treatment.
2 Mechanism of pathological changes in osteoarthritis
Pathological changes of OA are mainly reflected in the articular cartilage, subchondral bone and synovial membrane. Articular cartilage degeneration is the earliest pathological change of OA. The main manifestations include softening and cracks in the deep cartilage, with narrowing of the joint space in serious cases (14). The subchondral bone of OA patients also change. If the subchondral bone of OA patients is under excessive pressure, its density will increase, showing ivory sclerosis. In contrast, if the subchondral bone of OA patients is not stimulated by pressure for a long time, the bone density will decrease and eventually shrink. The subchondral bone of OA patients constantly changes with the variations of biological stress, thus forming osteophyte and leading to joint deformities (15). In addition, OA patients generally present with synovitis, mainly caused by the phagocytosis of small cartilage pieces that have fallen into the synovial fluid and joining synovial cells. Congestion and plasma cell infiltration may occur in the early stage, and foreign body giant cell reactions may occur in the later stage (16). These pathological changes are characteristics of OA. Many mechanisms are responsible for these pathological changes, including ECM degradation, apoptosis, inflammatory response, and autophagy.
2.1 Degradation of cartilage extracellular matrix
The ECM is a complex network consisting of various macromolecules around cells. Under normal circumstances, the synthesis and metabolism of cartilage extracellular matrix should always keep a dynamic balance. If the ECM of articular cartilage degrades, OA may be induced (17). Metalloproteinase with thrombus motifs, matrix metalloproteinase (MMPs), and Type II collagen are key proteins that induce ECM degradation of articular cartilage and play a key role in maintaining chondrocyte homeostasis (18). Numerous cytokines and non-coding RNA can induce OA by stimulating ECM degradation of articular cartilage. TGF-β is a cytokine which plays an important role in the growth and development of the articular cartilage. TGF-β can stimulate the production of ECM proteins and also block the ECM degradation proteins by increasing protease inhibitor production (19, 20). Therefore, the reduction of TGF-β can induce OA. In addition, many MicroRNAs, such as miR-140 (21), miR-146a (22) and miR-19b (23), can directly regulate chondrocytes and disrupt the balance between the anabolism and catabolism of ECM by affecting their upstream/downstream regulatory factors or pathways. Other studies have shown that chondrocytes will undergo different changes in metabolism after encountering external mechanical stimuli such as hypoxia (Abramson and Attur, 2009), which will eventually lead to the degradation of ECM (24).
2.2 Apoptosis
Many stimuli can cause apoptosis of chondrocytes, and a correlation exists between the damage degree of chondrocytes and apoptosis, and obvious apoptosis occurs in the cartilage of OA patients (25). On the one hand, OA cartilage can produce considerable nitric oxide (NO). Low-level reactive oxygen species (ROS) can induce apoptosis in the presence of NO, and high-level ROS can cause necrosis. On the other hand, mitochondria play a crucial role in cell function and survival, and the damage to the outer membrane of the mitochondria in OA chondrocytes will cause the release of apoptosis factors such as caspase-8 and caspase-9 into the cytoplasm from the gap of the mitochondrial membrane, eventually leading to cell apoptosis (26). Studies have proved that hypoxia can stimulate the generation of ROS in mitochondria of chondrocytes and induce apoptosis (7). In addition, various physical or chemical stimuli can regulate OA through biomarkers or signal pathways such as Bcl-2, Bax, JNK and MAPK that affect apoptosis. For example, Kong et al. (27) found that mechanical stimulation can promote the phosphorylation of JNK and MAPK and regulate the apoptosis of chondrocytes.
2.3 Autophagy
Furthermore, autophagy is closely related to apoptosis and can realize the metabolic needs of cells and the renewal of some organelles. In the early stage of OA, autophagy is activated to avoid apoptosis. In the late stage of OA, apoptosis increases extensively and can be activated at the same time as apoptosis (28). Numerous biomarkers, such as Beclin1, LC3, and P62, are related to autophagy. Takayama et al. (29) established an OA mouse model and treated the subjects with rapamycin. The results showed that the expression of mTOR decreased, LC3 was activated, and the severity of OA was reduced in rapamycin-treated mice. When oxidative stress occurs, cell autophagy will also be activated (30), and AMPK can directly regulate autophagy by acting on the downstream signal molecules of mTOR (31), an occurrence which ultimately affects the pathological process of OA. Studies have proved that oxidative stress and hypoxia can stimulate mitochondrial autophagy and promote cell survival (7).
2.4 Inflammatory reaction
Inflammation is the body’s response to infection, pathogenic microorganisms, trauma, allergy, and other tissues and cells and is also the body’s defensive response (32). For patients in the late stage of OA, pro-inflammatory cytokines and chemokines in synovial fluid increase (33), which could increase the expression of collagenase and aggrecan, induce the inflammatory reaction, and lead to the ECM degradation of articular cartilage (34). TNF, IL-1β, IL-6, and IL-15 are cytokines related to inflammation, and NF-κB, MAPK, and AMPK are common signal pathways to induce the inflammatory response. Some studies have found that regulating NF-κB/SIRT1/AMPK and MAPK/NF-κB signaling pathways can affect the inflammatory response and ultimately affect the pathological process of OA (35) (36). In addition, Hypoxia can also aggravate inflammatory reaction by affecting macrophages, T cells and neutrophils (37). Therefore, the changes of some cytokines and inflammation-related signaling pathways, or the hypoxia environment can aggravate the inflammatory reaction and ultimately affect the pathological process of OA.
In conclusion, the pathological changes of the articular cartilage, subchondral bone, and synovium in OA patients are generally caused by ECM degradation, apoptosis, autophagy and inflammatory reaction. As shown in Figure 1.
Figure 1 Pathological change mechanism of OA.
3 HIFs in pathological mechanism of osteoarthritis
HIFs have different mechanisms in normoxic and hypoxic environments, and they can alleviate the pathological process of osteoarthritis, as shown in Figure 2. Further, HIFs are closely related to the pathological mechanism of OA. Bouaziz et al. (38) and Yang et al. (39) proved the role of HIF-1-α and HIF-2-α in OA for the first time by using the mouse model of functional loss and functional gain respectively. HIFs and HIFs-related genes and signal pathways can participate in the pathological process of OA by affecting ECM degradation, apoptosis, autophagy, and inflammatory response. as shown in Table 1.
Figure 2 Mechanism of HIFs on OA in Normoxic and Hypoxic Environments.
Table 1 Functional characterization of the HIFs in OA.
3.1 HIFs in the degradation of cartilage extracellular matrix
HIFs may be involved in the ECM degradation of articular cartilage. In a hypoxic environment, chondrocytes can make an adaptive response to glycolysis through the HIF-α transcription factor. HIF-1α and HIF-2α are mainly expressed in chondrocytes. HIF-1α promotes cartilage homeostasis by maintaining anaerobic glycolysis, stabilizing articular cartilage phenotype, inducing proper autophagy, and inhibiting ECM degradation of articular cartilage (5). In OA cells, the increased HIF-1α expression can promote the increase of ECM of articular cartilage (67). For example, Kovács et al. (107) confirmed that when OA occurred, depriving the chondrocytes of oxygen could activate HIF-1α and promote ECM of articular cartilage synthesis. Hu et al. (7) established an OA mouse model and detected the levels of the HIF-1α gene and protein in vivo and in vitro experiments. They found that HIF-1α expression was up-regulated in human and mouse knee joint cartilage. HIF-1α can inhibit ECM degradation of articular cartilage by mediating mitochondrial autophagy, thereby alleviating the metabolic imbalance of ECM and finally clearing OA. However, HIF-2α is a catabolic transcription factor. It is involved in the formation of chondrocyte phenotype induced by hypoxia but has the effect of antagonizing part of HIF-1α. In OA, HIF-2α expression in articular cartilage increases, which encourages the catabolic reaction by promoting chondrocyte hypertrophy and differentiation and increasing the expression of MMP family-related factors (108).
Many studies have found that we can improve the ECM by regulating HIFs through some small molecules. Some protein molecules can regulate HIF-1α and participate in ECM degradation of articular cartilage. For example, pyruvate kinase M2(PKM2) can handle HIF-1α. Low PKM2 knockdown inhibits HIF-1α, which reduces the expression of COL2A1 and SOX-9 and ultimately accelerates the ECM degradation of articular cartilage (46). Some compounds can also regulate HIF-1α expression. For example, Icariin can increase HIF-1α expression, promote anaerobic glycolysis metabolism, increase cell vitality, and promote ECM of articular cartilage production (109). Both wogonin (88) and curcumin (77) can regulate ECM of articular cartilage homeostasis by inhibiting the NF-κB/HIF-2α axis and thus reduce OA progression.
A variety of non-coding RNAs can be involved in the ECM degradation of articular cartilage by mediating HIFs to promote the expression of related genes. Hwang et al. (94) studied human chondrocytes of OA patients. They found that compared with normal cartilage, human OA cartilage had a significantly decreased miR-365 level, increased HIF-2α mRNA level, and significantly increased level of HIF-2α positive cells. Therefore, the decreased expression level of miR-365 in OA can up-regulate the expression of HIF-2α, increase the expression of a variety of catabolic genes, and ultimately promote ECM degradation of articular cartilage. In addition, miR-455 expression is decreased in OA cartilage. MiR-455s can inhibit the expression of HIF-2α and increase the expression of genes related to cartilage degradation (75). HIF-3α also plays a role in regulating the ECM of articular cartilage. Li et al. (105) noted reduced expression of miR-210 in OA cartilage by reverse transcription-polymerase chain reaction (RT-PCR). Through the Western blot (WB) analysis, they further found that miR-210 overexpression could inhibit the mRNA and protein expression level of HIF-3α in OA chondrocytes. When the expression level of HIF-3α is decreased, the mRNA level of COL2A1 is increased and the mRNA levels of MMP13 are reduced, resulting in increased ECM deposition in OA chondrocytes. Therefore, some cytokines, small molecular compounds and non-coding RNA can affect the ECM degradation of articular cartilage by regulating HIFs.
3.2 HIFs in apoptosis of cartilage and bone
Some HIFs participate in the occurrence and development of OA by mediating apoptosis. Different HIFs subtypes have different effects on chondrocyte apoptosis in a hypoxic environment. For example, HIF-1α can inhibit chondrocyte apoptosis, while HIF-2α can promote chondrocyte apoptosis in the hypoxic environment. It is necessary to detect the expression of HIFs in degenerative articular cartilage. Huang et al. (110) intervened in chondrocytes with hypoxia and found that the expressions of HIF-1α and HIF-2α were up-regulated, and the apoptosis rate of chondrocytes increased. In chondrocytes and tissues, HIF-3α is negatively correlated with hypertrophy markers COL10A1 and MMP13. In OA chondrocytes, HIF-3α expression is lower than that of healthy chondrocytes, and MMP13 expression is higher, resulting in a high apoptosis rate (111). In a mouse model of OA induced by mechanical stress, researchers found that the expression of HIF-1α decreased and the expression of caspase 3 increased in the chondrocytes of OA mice and concluded that the HIF-1α signal might participate in chondrocyte apoptosis by inhibiting the caspase cascade and slowing down the process of OA (65).
In addition to a hypoxic environment, many cytokines and growth factors can stabilize and activate HIF-1α, such as the chondrocyte catabolism factors IL-1β and TNF-α. Stimulation of cultured synovial fibroblasts with IL-1β and TNF-α increase HIF-1α mRNA levels. The enhancement of HIF-1α activity can promote energy production and cartilage matrix protein synthesis in OA chondrocytes under hypoxia and can also enhance the expression of anti-apoptosis factors (45). Therefore, many cytokines, protein molecules, and small molecular compounds can accelerate or inhibit apoptosis by regulating HIFs, thereby exerting a certain impact on OA. For example, through immunohistochemistry, WB, and RT-PCR, Ma et al. (48) discovered that the increased Bmal1 expression in mouse Osteoarthritis chondrocytes could up-regulate HIF1α and HIF2α expression, inhibit the levels of MMP13 mRNA and protein, impede apoptosis, and alleviate the process of OA. Yang et al. (84) measured the mRNA and protein expression levels of HIF-2α in mouse OA chondrocytes and confirmed that HIF-2α was up-regulated in OA chondrocytes compared with that of normal cells. Platelet-rich plasma (PRP) inhibits the activation of HIF-2α by reducing the expression of apoptotic markers such as MMP3 and MMP13. Therefore, PRP can reduce the IL-1β-induced apoptosis of chondrocytes by inhibiting HIF-2α. Ryu et al. (9) noted significantly increased levels of HIF-2α in human and mouse OA chondrocytes. Overexpression or knock-down of HIF-2α alone does not induce apoptosis in chondrocytes. However, HIF-2α expression significantly increases chondrocyte apoptosis in the presence of agnostic anti-Fas antibody. Thus, HIF-2α can enhance Fas-mediated apoptosis of chondrocytes and aggravate the pathological process of OA.
Activation of HIF-related signaling pathways may also accelerate or inhibit apoptosis. Using an OA mouse model, Rong et al. (44) found that miR-216a-5p expression was increased in small extracellular vesicles and then gradually transferred to chondrocytes. JAK2 is a target gene of miR-216a-5p. Through the miR -216a-5p/JAK 2/STAT 3 signaling pathway, HIF-1α can induce hypoxic bone marrow mesenchymal stem cells to release small extracellular vesicles and inhibit the apoptosis of chondrocytes. In addition, OA chondrocytes can promote the migration of vascular endothelial cells under the stimulation of TNF-α by secreting chemokines and vascular endothelial growth factors. The invasion of vascular endothelial cells leads to an increase in oxygen tension in the local environment, which activates the JAK-STAT5 pathway. Moreover, the binding of phosphorylated STAT5 to specific sites in the SED7 promoter increases the transcription of SED7. SED7 mediates chondrocyte apoptosis by inhibiting the nuclear localization of HIF-1α and participates in the occurrence and development of OA (112).
Some non-coding RNAs are also involved in apoptosis by mediating HIFs. Song et al. (113) found that in the articular chondrocytes of mice knocked out by HIF-1α, the expression level of CRAT was decreased and that of miR-144-3p was increased. Through further observation and analysis of the articular chondrocytes, they confirmed an increase in the apoptosis of chondrocytes. Therefore, HIF-1α overexpression can stimulate CRAT expression and inhibit miR-144-3p expression, thereby inhibiting apoptosis and ultimately alleviating OA. VEGF and BNIP3 are target genes of HIF-1α. LncHIFCAR promotes hypoxia-induced inflammatory response and matrix synthesis by upregulating VEGF and induces apoptosis by upregulating BNIP3. LncHIFCAR is up-regulated in OA tissues, and LncHIFCAR inhibition may improve hypoxia-induced apoptosis and cell damage and alleviate OA progression by positively regulating HIF-1α and HIF-1α target genes (VEGF and BNIP3) (57). Chen et al. (60) took human chondrocytes and induced an OA chondrocyte model by LPS. They found significantly increased expression levels of circRNA-UBE2G1 and HIF-1α in OA tissues and down-regulated expression levels of miR-373. CircRNA-UBE2G1 binds to miR-373 as competitive endogenous RNA (ceRNA). HIF-1α may also be a target for miR-373. Therefore, circRNA-UBE2G1 can induce apoptosis and ultimately accelerate the OA progression by regulating the miR-373/HIF-1α axis. Therefore, some cytokines, small molecular compounds and non-coding RNA can affect the apoptosis by regulating HIFs.
3.3 HIFs in inflammatory response
HIFs are closely related to the inflammatory response in OA. Many genes, proteins, and compounds can participate in the inflammatory response by regulating HIF-1α. Under hypoxic conditions, HIF-1α expression is up-regulated in OA synovial fibroblasts, leading to inflammatory cell recruitment and angiogenesis (114). High-mobility group 1 protein (HMGB1) is a protein associated with inflammation. Feng et al. (61) stimulated rat synovial fibroblasts with HMGB1 to investigate the expression of VEGF and HIF-1α in these cells by using WB, RT-PCR, and immunofluorescence. They verified that inflammatory factors such as IL-6, IL-1β, and TNF-α were increased in rat synovial fluid. Moreover, by activating Erk and JNK, HMGB1 up-regulated VEGF and HIF-1α in OA synovial fibroblasts to participate in the inflammatory response. Some compounds can affect inflammatory response by regulating HIFs. The expression of HIF-1α, NLRP3, and IL-1β increases in the absence of oxygen. Imperatorin (IMP) can alleviate synovitis and synovial fibrosis and improve the symptoms of OA by inhibiting HIF-1α/NLRP3 inflammasome signaling (115). Agnuside ameliorated the hypoxia in KOA rats and inhibited the accumulation of HIF-1 α and activation of NLRP3 inflammasome in LPS-treated fibroblast-like synovial cells, thereby alleviating synovitis in KOA rats and alleviating the pathological conditions of OA (43). Li et al. (66) established an OA rat model, intervened with casticin, and detected the inflammatory components and the expression of HIF-1α by using WB, RT-PCR, or ELISA. The results showed that capsaicin inhibited the MIA-induced activation of NLRP3 inflammasomes in OA rats and synovial fibroblasts, inhibited the expression of HIF-1α, and reduced the hypoxia and inflammation of synovial tissue in rats, finally alleviating OA.
In addition, proper exercise and some compounds can also affect the inflammatory response by regulating HIF-2α. Wang et al. (116) established an OA rat model and applied whole-body shaking exercises at different frequencies to detect the expression of relevant genes and proteins by using RT-PCR and WB. They found that in the early OA knee joint cartilage, whole-body vibration training could reduce the levels of inflammatory factors, inhibit HIF-2α expression, and alleviate the pathological changes of the OA cartilage. Through in vivo and in vitro experiments, Cho et al. (81) demonstrated that apigenin could effectively reduce HiF-2α expression and inhibit the manifestations of IL-6 and COX-2 in HIF-2α-induced articular chondrocytes, thereby reducing inflammation and relieving OA. Therefore, many compounds can slow down the inflammatory reaction by regulating different subtypes of HIFs.
3.4 HIFs in autophagy
HIFs are closely related to autophagy. Lu et al. (58) took human OA chondrocytes induced by IL-1β and conducted an in vitro experiment. They found high basal autophagy levels in chondrocytes in an environment with elevated HIF-1α, and the chondrocytes were resistant to IL-1β-induced inflammatory damage. Some special environments and compounds can participate in autophagy by regulating HIFs. Moussa et al. (72) cultured human OA chondrocytes in PRP. RT-PCR and ELISA detected the expressions of autophagy markers such as BECLIN, LC3II, and HIF-1. They finally found that the terms of autophagy markers BECLIN and LC3II were up-regulated, as well as the expression of HIF-1 mRNA. Therefore, PRP can participate in cartilage protection and alleviate OA by up-regulating HIF-1 and promoting autophagy. Qin et al. (103) established an OA mouse model and judged the effect of resveratrol on autophagy and HIF expression by injecting resveratrol into the joint cavity. They confirmed that resveratrol delayed articular cartilage degeneration and promoted chondrocyte autophagy, which could balance the expression of HIF-1α and HIF-2α and ultimately regulate the AMPK/mTOR signaling pathway to protect articular cartilage.
Some non-coding RNA can also be involved in autophagy by mediating HIFs. MiR-146a and HIF-1α expression were up-regulated when the chondrocytes of OA mice were exposed to hypoxia. RT-PCR and WB revealed that miR-146a could induce HIF-1α expression in hypoxia and then promote autophagy by reducing the expression of autophagy inhibitor Bcl-2 and finally alleviate OA (40, 69). By TargetScan analysis, Yang et al. (71) experimented with human OA chondrocytes and revealed that HIF-1α mRNA was the direct target of miR-411. They further verified that miR-411 could directly recognize the predicted HIF-1α mRNA site and inhibit HIF-1α expression in chondrocytes through luciferase reporter gene detection. Therefore, miR-411 promotes chondrocyte autophagy by targeting HIF-1α. Therefore, some special environments, compounds or non-coding RNA can participate in autophagy by regulating HIFs.
4 Conclusion and prospect
Hypoxia and HIFs participate in a series of pathophysiological processes such as cartilage destruction, synovial inflammation, and angiogenesis in OA. Therefore, HIFs may be closely related to the pathological mechanism of OA. With increasing in-depth research on HIFs, their regulatory role in cartilage physiology and pathology gradually becomes clear, and HIFs can participate in various signal pathways to regulate the survival and metabolism of chondrocytes. HIFs can affect the pathological changes of articular cartilage, subchondral bone, and synovium by participating in ECM degradation of articular cartilage, apoptosis, inflammatory reaction, and autophagy. Moreover, HIFs play an essential role in the pathological changes of OA.
Although a growing number of studies have been conducted on the metabolism, growth, and apoptosis of articular cartilage, the study on the role of HIFs in disease regulation, diagnosis and treatment remains in the early stage (117), and many problems need to be solved urgently. First, under different oxygen concentrations, different levels of chondrocytes have distinct responses to oxygen concentrations, so researchers should explore appropriate oxygen concentrations to promote cartilage repair at different levels (118). Second, cartilage repair is a complex process influenced by many factors, so further study on the combination of HIFs and other growth factors need to be made to promote cartilage repair (71). Moreover, the effects of different subtypes of HIFs on chondrocytes vary in a hypoxic environment and the role of each subtype in cartilage repair should be further explored. Finally, the functions of HIFs in different stages of OA may be different, and the subtypes of HIFs should be selectively used to delay the progression of OA in each stage of the disease (119).
As for the future, with the role of different oxygen concentrations, subtypes of HIFs, and combined use of various growth factors in cartilage repair becoming increasingly clear, researchers can consider HIFs as the therapeutic target of OA, an approach which will achieve further breakthroughs and progress in OA treatment. This review summarizes the role of HIFs in ECM degradation, apoptosis, inflammation, and autophagy of OA and expounds on the current research progress of HIFs in the prevention, diagnosis, and treatment of OA, thereby providing a basis for the future treatment of OA with HIFs.
Author contributions
X-AZ: conceptualization, project administration, and funding acquisition. HK and X-AZ: writing – review and editing. All authors contributed to the article and approved the submitted version. HK and X-AZ contributed equally to the article and should be regarded as co-first authors.
Funding
The work was supported by the Innovative Talents Support Program for Universities of Liaoning Province, No.WR2019024.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
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References
1. Xia B, Di C, Zhang J, Hu S, Jin H, Tong P. Osteoarthritis pathogenesis: a review of molecular mechanisms. Calcif Tissue Int (2014) 95(6):495–505. doi: 10.1007/s00223-014-9917-9
2. Prieto-Alhambra D, Judge A, Javaid MK, Cooper C, Diez-Perez A, Arden NK. Incidence and risk factors for clinically diagnosed knee, hip and hand osteoarthritis: Influences of age, gender and osteoarthritis affecting other joints. Ann Rheum Dis (2014) 73(9):1659–64. doi: 10.1136/annrheumdis-2013-203355
3. Abramoff B, Caldera FE. Osteoarthritis: Pathology, diagnosis, and treatment options. Med Clin North Am (2020) 104(2):293–311. doi: 10.1016/j.mcna.2019.10.007
4. Brooks PM, March LM. New insights into osteoarthritis. Med J Aust (1995) 163(7):367–9. doi: 10.5694/j.1326-5377.1995.tb124631.x
5. Zhang F-J, Luo W, Lei G-H. Role of HIF-1α and HIF-2α in osteoarthritis. Joint Bone Spine. (2015) 82(3):144–7. doi: 10.1016/j.jbspin.2014.10.003
6. Cowman SJ, Koh MY. Revisiting the HIF switch in the tumor and its immune microenvironment. Trends Cancer. (2022) 8(1):28–42. doi: 10.1016/j.trecan.2021.10.004
7. Hu S, Zhang C, Ni L, Huang C, Chen D, Shi K, et al. Stabilization of HIF-1α alleviates osteoarthritis via enhancing mitophagy. Cell Death Dis (2020) 11(6):481. doi: 10.1038/s41419-020-2680-0
8. Chen Y, Zhao B, Zhu Y, Zhao H, Ma C. HIF-1-VEGF-Notch mediates angiogenesis in temporomandibular joint osteoarthritis. Am J Transl Res (2019) 11(5):2969–82.
9. Ryu JH, Shin Y, Huh YH, Yang S, Chun CH, Chun JS. Hypoxia-inducible factor-2α regulates fas-mediated chondrocyte apoptosis during osteoarthritic cartilage destruction. Cell Death Differ (2012) 19(3):440–50. doi: 10.1038/cdd.2011.111
10. Saito T, Kawaguchi H. HIF-2α as a possible therapeutic target of osteoarthritis. Osteoarthritis Cartilage. (2010) 18(12):1552–6. doi: 10.1016/j.joca.2010.10.006
11. Charlier E, Relic B, Deroyer C, Malaise O, Neuville S, Collée J, et al. Insights on molecular mechanisms of chondrocytes death in osteoarthritis. Int J Mol Sci (2016) 17(12). doi: 10.3390/ijms17122146
12. Fernández-Torres J, Zamudio-Cuevas Y, Martínez-Nava GA, López-Reyes AG. Hypoxia-inducible factors (HIFs) in the articular cartilage: A systematic review. Eur Rev Med Pharmacol Sci (2017) 21(12):2800–10.
13. Augstein A, Poitz DM, Braun-Dullaeus RC, Strasser RH, Schmeisser A. Cell-specific and hypoxia-dependent regulation of human HIF-3α: inhibition of the expression of HIF target genes in vascular cells. Cell Mol Life Sci (2011) 68(15):2627–42. doi: 10.1007/s00018-010-0575-4
14. Martin DF. Pathomechanics of knee osteoarthritis. Med Sci Sports Exerc. (1994) 26(12):1429–34. doi: 10.1249/00005768-199412000-00003
15. Hu Y, Chen X, Wang S, Jing Y, Su J. Subchondral bone microenvironment in osteoarthritis and pain. Bone Res (2021) 9(1):20. doi: 10.1038/s41413-021-00147-z
16. Mathiessen A, Conaghan PG. Synovitis in osteoarthritis: Current understanding with therapeutic implications. Arthritis Res Ther (2017) 19(1):18. doi: 10.1186/s13075-017-1229-9
17. Li SH, Wu QF. MicroRNAs target on cartilage extracellular matrix degradation of knee osteoarthritis. Eur Rev Med Pharmacol Sci (2021) 25(3):1185–97. doi: 10.26355/eurrev_202102_24821
18. Yang CY, Chanalaris A, Troeberg L. ADAMTS and ADAM metalloproteinases in osteoarthritis - looking beyond the 'usual suspects'. Osteoarthritis Cartilage. (2017) 25(7):1000–9. doi: 10.1016/j.joca.2017.02.791
19. van der Kraan PM, Blaney Davidson EN, Blom A, van den Berg WB. TGF-beta signaling in chondrocyte terminal differentiation and osteoarthritis: Modulation and integration of signaling pathways through receptor-smads. Osteoarthritis Cartilage. (2009) 17(12):1539–45. doi: 10.1016/j.joca.2009.06.008
20. Blaney Davidson EN, van der Kraan PM, van den Berg WB. TGF-beta and osteoarthritis. Osteoarthritis Cartilage. (2007) 15(6):597–604. doi: 10.1016/j.joca.2007.02.005
21. Nilsson S, Mäkelä S, Treuter E, Tujague M, Thomsen J, Andersson G, et al. Mechanisms of estrogen action. Physiol Rev (2001) 81(4):1535–65. doi: 10.1152/physrev.2001.81.4.1535
22. Taganov KD, Boldin MP, Chang K-J, Baltimore D. NF-kappaB-dependent induction of microRNA miR-146, an inhibitor targeted to signaling proteins of innate immune responses. Proc Natl Acad Sci U S A. (2006) 103(33):12481–6. doi: 10.1073/pnas.0605298103
23. Zhou Y, Li R-J, Li M, Liu X, Zhu H-Y, Ju Z, et al. Overexpression of GRK6 attenuates neuropathic pain via suppression of CXCR2 in rat dorsal root ganglion. Mol Pain. (2016) 12. doi: 10.1177/1744806916646381
24. Abramson SB, Attur M. Developments in the scientific understanding of osteoarthritis. Arthritis Res Ther (2009) 11(3):227. doi: 10.1186/ar2655
25. Del Carlo M, Loeser RF. Nitric oxide-mediated chondrocyte cell death requires the generation of additional reactive oxygen species. Arthritis Rheumatol (2002) 46(2):394–403. doi: 10.1002/art.10056
26. Grishko VI, Druzhyna N, LeDoux SP, Wilson GL. Nitric oxide-induced damage to mtDNA and its subsequent repair. Nucleic Acids Res (1999) 27(22):4510–6. doi: 10.1093/nar/27.22.4510
27. Kong D, Zheng T, Zhang M, Wang D, Du S, Li X, et al. Static mechanical stress induces apoptosis in rat endplate chondrocytes through MAPK and mitochondria-dependent caspase activation signaling pathways. PloS One (2013) 8(7):e69403. doi: 10.1371/journal.pone.0069403
28. Almonte-Becerril M, Navarro-Garcia F, Gonzalez-Robles A, Vega-Lopez MA, Lavalle C, Kouri JB. Cell death of chondrocytes is a combination between apoptosis and autophagy during the pathogenesis of osteoarthritis within an experimental model. Apoptosis. (2010) 15(5):631–8. doi: 10.1007/s10495-010-0458-z
29. Takayama K, Kawakami Y, Kobayashi M, Greco N, Cummins JH, Matsushita T, et al. Local intra-articular injection of rapamycin delays articular cartilage degeneration in a murine model of osteoarthritis. Arthritis Res Ther (2014) 16(6):482. doi: 10.1186/s13075-014-0482-4
30. Roca-Agujetas V, de Dios C, Lestón L, Marí M, Morales A, Colell A. Recent insights into the mitochondrial role in autophagy and its regulation by oxidative stress. Oxid Med Cell Longev (2019) 2019:3809308. doi: 10.1155/2019/3809308
31. Alers S, Löffler AS, Wesselborg S, Stork B. Role of AMPK-mTOR-Ulk1/2 in the regulation of autophagy: Cross talk, shortcuts, and feedbacks. Mol Cell Biol (2012) 32(1):2–11. doi: 10.1128/MCB.06159-11
32. Lieberthal J, Sambamurthy N, Scanzello CR. Inflammation in joint injury and post-traumatic osteoarthritis. Osteoarthritis Cartilage. (2015) 23(11):1825–34. doi: 10.1016/j.joca.2015.08.015
33. Greene MA, Loeser RF. Aging-related inflammation in osteoarthritis. Osteoarthritis Cartilage. (2015) 23(11):1966–71. doi: 10.1016/j.joca.2015.01.008
34. Khan NM, Haseeb A, Ansari MY, Devarapalli P, Haynie S, Haqqi TM. Wogonin, a plant derived small molecule, exerts potent anti-inflammatory and chondroprotective effects through the activation of ROS/ERK/Nrf2 signaling pathways in human osteoarthritis chondrocytes. Free Radic Biol Med (2017) 106:288–301. doi: 10.1016/j.freeradbiomed.2017.02.041
35. Wang C, Gao Y, Zhang Z, Chi Q, Liu Y, Yang L, et al. Safflower yellow alleviates osteoarthritis and prevents inflammation by inhibiting PGE2 release and regulating NF-κB/SIRT1/AMPK signaling pathways. Phytomedicine. (2020) 78:153305. doi: 10.1016/j.phymed.2020.153305
36. Yao M, Zhang C, Ni L, Ji X, Hong J, Chen Y, et al. Cepharanthine ameliorates chondrocytic inflammation and osteoarthritis via regulating the MAPK/NF-κB-Autophagy pathway. Front Pharmacol (2022) 13:854239. doi: 10.3389/fphar.2022.854239
37. McGettrick AF, O'Neill LAJ. The role of HIF in immunity and inflammation. Cell Metab (2020) 32(4):524–36. doi: 10.1016/j.cmet.2020.08.002
38. Bouaziz W, Sigaux J, Modrowski D, Devignes C-S, Funck-Brentano T, Richette P, et al. Interaction of HIF1α and β-catenin inhibits matrix metalloproteinase 13 expression and prevents cartilage damage in mice. Proc Natl Acad Sci U S A. (2016) 113(19):5453–8. doi: 10.1073/pnas.1514854113
39. Yang S, Kim J, Ryu J-H, Oh H, Chun C-H, Kim BJ, et al. Hypoxia-inducible factor-2alpha is a catabolic regulator of osteoarthritic cartilage destruction. Nat Med (2010) 16(6):687–93. doi: 10.1038/nm.2153
40. Chen G, Gao X, Wang J, Yang C, Wang Y, Liu Y, et al. Hypoxia-induced microRNA-146a represses bcl-2 through Traf6/IRAK1 but not Smad4 to promote chondrocyte autophagy. Biol Chem (2017) 398(4):499–507. doi: 10.1515/hsz-2016-0211
41. Tong J, Deng C, Sun G, Zhou J, Zhong P, Wang T, et al. Electroacupuncture upregulates HIF-1 and SOX9 expression in knee osteoarthritis. Evid Based Complement Alternat Med (2021) 2021:2047097. doi: 10.1155/2021/2047097
42. Zhang L, Zhang L, Huang Z, Xing R, Li X, Yin S, et al. Increased HIF-1 in knee osteoarthritis aggravate synovial fibrosis via fibroblast-like synoviocyte pyroptosis. Oxid Med Cell Longev (2019) 2019:6326517. doi: 10.1155/2019/6326517
43. Zhang L, Li X, Zhang H, Huang Z, Zhang N, Zhang L, et al. Agnuside alleviates synovitis and fibrosis in knee osteoarthritis through the inhibition of HIF-1 and NLRP3 inflammasome. Mediators Inflamm (2021) 2021:5534614. doi: 10.1155/2021/5534614
44. Rong Y, Zhang J, Jiang D, Ji C, Liu W, Wang J, et al. Hypoxic pretreatment of small extracellular vesicles mediates cartilage repair in osteoarthritis by delivering miR-216a-5p. Acta Biomater. (2021) 122:325–42. doi: 10.1016/j.actbio.2020.12.034
45. Yudoh K, Nakamura H, Masuko-Hongo K, Kato T, Nishioka K. Catabolic stress induces expression of hypoxia-inducible factor (HIF)-1 alpha in articular chondrocytes: Involvement of HIF-1 alpha in the pathogenesis of osteoarthritis. Arthritis Res Ther (2005) 7(4):R904–R14. doi: 10.1186/ar1765
46. Yang X, Chen W, Zhao X, Chen L, Li W, Ran J, et al. Pyruvate kinase M2 modulates the glycolysis of chondrocyte and extracellular matrix in osteoarthritis. DNA Cell Biol (2018) 37(3):271–7. doi: 10.1089/dna.2017.4048
47. Lin J-L, Wang MJ, Lee D, Liang C-C, Lin S. Hypoxia-inducible factor-1alpha regulates matrix metalloproteinase-1 activity in human bone marrow-derived mesenchymal stem cells. FEBS Lett (2008) 582(17):2615–9. doi: 10.1016/j.febslet.2008.06.033
48. Ma Z, Jin X, Qian Z, Li F, Xu M, Zhang Y, et al. Deletion of clock gene Bmal1 impaired the chondrocyte function due to disruption of the HIF1α-VEGF signaling pathway. Cell Cycle (2019) 18(13):1473–89. doi: 10.1080/15384101.2019.1620572
49. Zhang Y, Li S, Jin P, Shang T, Sun R, Lu L, et al. Dual functions of microRNA-17 in maintaining cartilage homeostasis and protection against osteoarthritis. Nat Commun (2022) 13(1):2447. doi: 10.1038/s41467-022-30119-8
50. Chen C-W, Sun J, Li Y-M, Shen P-A, Chen Y-Q. Action mechanisms of du-huo-ji-sheng-tang on cartilage degradation in a rabbit model of osteoarthritis. Evid Based Complement Alternat Med (2011) 2011:571479. doi: 10.1093/ecam/neq002
51. Shirakura M, Tanimoto K, Eguchi H, Miyauchi M, Nakamura H, Hiyama K, et al. Activation of the hypoxia-inducible factor-1 in overloaded temporomandibular joint, and induction of osteoclastogenesis. Biochem Biophys Res Commun (2010) 393(4):800–5. doi: 10.1016/j.bbrc.2010.02.086
52. Ichimaru S, Nakagawa S, Arai Y, Kishida T, Shin-Ya M, Honjo K, et al. Hypoxia potentiates anabolic effects of exogenous hyaluronic acid in rat articular cartilage. Int J Mol Sci (2016) 17(7):1013. doi: 10.3390/ijms17071013
53. Sartori-Cintra AR, Mara C, Argolo DL, Coimbra IB. Regulation of hypoxia-inducible factor-1α (HIF-1α) expression by interleukin-1β (IL-1 β), insulin-like growth factors I (IGF-I) and II (IGF-II) in human osteoarthritic chondrocytes. Clinics (Sao Paulo). (2012) 67(1):35–40. doi: 10.6061/clinics/2012(01)06
54. Lin Y-M, Huang Y-L, Fong Y-C, Tsai C-H, Chou M-C, Tang C-H. Hepatocyte growth factor increases vascular endothelial growth factor-a production in human synovial fibroblasts through c-met receptor pathway. PloS One (2012) 7(11):e50924. doi: 10.1371/journal.pone.0050924
55. Gelse K, Pfander D, Obier S, Knaup KX, Wiesener M, Hennig FF, et al. Role of hypoxia-inducible factor 1 alpha in the integrity of articular cartilage in murine knee joints. Arthritis Res Ther (2008) 10(5):R111. doi: 10.1186/ar2508
56. Song J, Kang Y-H, Yoon S, Chun C-H, Jin E-J. Correction: HIF-1α:CRAT:miR-144-3p axis dysregulation promotes osteoarthritis chondrocyte apoptosis and VLCFA accumulation. Oncotarget. (2019) 10(44):4609–10. doi: 10.18632/oncotarget.27091
57. Sun J, Song X, Su L, Cao S. Long non-coding RNA LncHIFCAR promotes osteoarthritis development via positively regulating HIF-1α and activating the PI3K/AKT/mTOR pathway. Int J Clin Exp Pathol (2018) 11(6):3000–9.
58. Lu J, Peng Y, Zou J, Wang J, Lu S, Fu T, et al. Hypoxia inducible factor-1α is a regulator of autophagy in osteoarthritic chondrocytes. Cartilage (2021) 13(2_suppl):1030S–40S. doi: 10.1177/19476035211035434
59. Shimomura S, Inoue H, Arai Y, Nakagawa S, Fujii Y, Kishida T, et al. Mechanical stimulation of chondrocytes regulates HIF-1α under hypoxic conditions. Tissue Cell (2021) 71:101574. doi: 10.1016/j.tice.2021.101574
60. Chen G, Liu T, Yu B, Wang B, Peng Q. CircRNA-UBE2G1 regulates LPS-induced osteoarthritis through miR-373/HIF-1a axis. Cell Cycle (2020) 19(13):1696–705. doi: 10.1080/15384101.2020.1772545
61. Feng Y, Hu S, Liu L, Ke J, Long X. HMGB1 contributes to osteoarthritis of temporomandibular joint by inducing synovial angiogenesis. J Oral Rehabil. (2021) 48(5):551–9. doi: 10.1111/joor.13129
62. Okada K, Mori D, Makii Y, Nakamoto H, Murahashi Y, Yano F, et al. Hypoxia-inducible factor-1 alpha maintains mouse articular cartilage through suppression of NF-κB signaling. Sci Rep (2020) 10(1):5425. doi: 10.1038/s41598-020-62463-4
63. Li L, Pang Y, Zhang L, Li M, Zhu C, Fang S, et al. Triiodothyronine potentiates angiogenesis-related factor expression through PI3K/AKT signaling pathway in human osteoarthritic osteoblasts. Iran J Basic Med Sci (2020) 23(6):819–25. doi: 10.22038/ijbms.2020.43634
64. Huang H, Zhang Z-F, Qin F-W, Tang W, Liu D-H, Wu P-Y, et al. Icariin inhibits chondrocyte apoptosis and angiogenesis by regulating the TDP-43 signaling pathway. Mol Genet Genomic Med (2019) 7(4):e00586. doi: 10.1002/mgg3.586
65. Mino-Oka A, Izawa T, Shinohara T, Mori H, Yasue A, Tomita S, et al. Roles of hypoxia inducible factor-1α in the temporomandibular joint. Arch Oral Biol (2017) 73:274–81. doi: 10.1016/j.archoralbio.2016.10.028
66. Li X, Mei W, Huang Z, Zhang L, Zhang L, Xu B, et al. Casticin suppresses monoiodoacetic acid-induced knee osteoarthritis through inhibiting HIF-1α/NLRP3 inflammasome signaling. Int Immunopharmacol. (2020) 86:106745. doi: 10.1016/j.intimp.2020.106745
67. Wang P, Zhu P, Liu R, Meng Q, Li S. Baicalin promotes extracellular matrix synthesis in chondrocytes via the activation of hypoxia-inducible factor-1α. Exp Ther Med (2020) 20(6):226. doi: 10.3892/etm.2020.9356
68. Yang H, Huang J, Mao Y, Wang L, Li R, Ha C. Vitexin alleviates interleukin-1β-induced inflammatory responses in chondrocytes from osteoarthritis patients: Involvement of HIF-1α pathway. Scand J Immunol (2019) 90(2):e12773. doi: 10.1111/sji.12773
69. Zhang F, Wang J, Chu J, Yang C, Xiao H, Zhao C, et al. MicroRNA-146a induced by hypoxia promotes chondrocyte autophagy through bcl-2. Cell Physiol Biochem (2015) 37(4):1442–53. doi: 10.1159/000438513
70. Li Q, Wen Y, Wang L, Chen B, Chen J, Wang H, et al. Hyperglycemia-induced accumulation of advanced glycosylation end products in fibroblast-like synoviocytes promotes knee osteoarthritis. Exp Mol Med (2021) 53(11):1735–47. doi: 10.1038/s12276-021-00697-6
71. Yang F, Huang R, Ma H, Zhao X, Wang G. miRNA-411 regulates chondrocyte autophagy in osteoarthritis by targeting hypoxia-inducible factor 1 alpha (HIF-1α). Med Sci Monit (2020) 26:e921155. doi: 10.12659/MSM.921155
72. Moussa M, Lajeunesse D, Hilal G, El Atat O, Haykal G, Serhal R, et al. Platelet rich plasma (PRP) induces chondroprotection via increasing autophagy, anti-inflammatory markers, and decreasing apoptosis in human osteoarthritic cartilage. Exp Cell Res (2017) 352(1):146–56. doi: 10.1016/j.yexcr.2017.02.012
73. Mousaei Ghasroldasht M, Moayednia A, Shahrezaee M. Effectiveness of platelet-ich plasma based on gene expression in knee osteoarthritis. Arch Bone Jt Surg (2019) 7(5):435–40.
74. Zhou X, Zheng Y, Sun W, Zhang Z, Liu J, Yang W, et al. D-mannose alleviates osteoarthritis progression by inhibiting chondrocyte ferroptosis in a HIF-2α-dependent manner. Cell Prolif. (2021) 54(11):e13134. doi: 10.1111/cpr.13134
75. Ito Y, Matsuzaki T, Ayabe F, Mokuda S, Kurimoto R, Matsushima T, et al. Both microRNA-455-5p and -3p repress hypoxia-inducible factor-2α expression and coordinately regulate cartilage homeostasis. Nat Commun (2021) 12(1):4148.
76. Chern C-M, Zhou H, Wang Y-H, Chang C-L, Chiou W-F, Chang W-T, et al. Osthole ameliorates cartilage degradation by downregulation of NF-κB and HIF-2α pathways in an osteoarthritis murine model. Eur J Pharmacol (2020) 867:172799. doi: 10.1016/j.ejphar.2019.172799
77. Zhou Y, Ming J, Deng M, Li Y, Li B, Li J, et al. Chemically modified curcumin (CMC2.24) alleviates osteoarthritis progression by restoring cartilage homeostasis and inhibiting chondrocyte apoptosis via the NF-κB/HIF-2α axis. J Mol Med (Berl) (2020) 98(10):1479–91. doi: 10.1007/s00109-020-01972-1
78. Li W, Wu N, Wang J, Wang Y, Wu M, Wang H. Role of HIF-2α/NF-κB pathway in mechanical stress-induced temporomandibular joint osteoarthritis. Oral Dis (2021) 28(8):2239–47. doi: 10.1111/odi.13986
79. Lee M, Won Y, Shin Y, Kim JH, Chun JS. Reciprocal activation of hypoxia-inducible factor (HIF)-2α and the zinc-ZIP8-MTF1 axis amplifies catabolic signaling in osteoarthritis. Osteoarthritis Cartilage. (2016) 24(1):134–45. doi: 10.1016/j.joca.2015.07.016
80. Wang K, Li Y, Dai Y, Han L, Zhu Y, Xue C, et al. Peptides from Antarctic krill ( euphausia superba) improve osteoarthritis via inhibiting HIF-2α-Mediated death receptor apoptosis and metabolism regulation in osteoarthritic mice. J Agric Food Chem (2019) 67(11):3125–33. doi: 10.1021/acs.jafc.8b05841
81. Cho C, Kang L-J, Jang D, Jeon J, Lee H, Choi S, et al. Cirsium japonicum var. maackii and apigenin block hif-2α-induced osteoarthritic cartilage destruction. J Cell Mol Med (2019) 23(8):5369–79. doi: 10.1111/jcmm.14418
82. Sperry MM, Yu Y-H, Kartha S, Ghimire P, Welch RL, Winkelstein BA, et al. Intra-articular etanercept attenuates pain and hypoxia from TMJ loading in the rat. J Orthop Res (2020) 38(6):1316–26. doi: 10.1002/jor.24581
83. Li W, Cai L, Zhang Y, Cui L, Shen G. Intra-articular resveratrol injection prevents osteoarthritis progression in a mouse model by activating SIRT1 and thereby silencing HIF-2α. J Orthop Res (2015) 33(7):1061–70. doi: 10.1002/jor.22859
84. Yang J, Guo A, Li Q, Wu J. Platelet-rich plasma attenuates interleukin-1β-induced apoptosis and inflammation in chondrocytes through targeting hypoxia-inducible factor-2α. Tissue Cell (2021) 73:101646. doi: 10.1016/j.tice.2021.101646
85. Yang Q, Zhou Y, Cai P, Fu W, Wang J, Wei Q, et al. Up-regulated HIF-2α contributes to the osteoarthritis development through mediating the primary cilia loss. Int Immunopharmacol. (2019) 75:105762. doi: 10.1016/j.intimp.2019.105762
86. Zhou K, He S, Yu H, Pei F, Zhou Z. Inhibition of syndecan-4 reduces cartilage degradation in murine models of osteoarthritis through the downregulation of HIF-2α by miR-96-5p. Lab Invest. (2021) 101(8):1060–70. doi: 10.1038/s41374-021-00595-5
87. Zhang X, Prasadam I, Fang W, Crawford R, Xiao Y. Chondromodulin-1 ameliorates osteoarthritis progression by inhibiting HIF-2α activity. Osteoarthritis Cartilage. (2016) 24(11):1970–80. doi: 10.1016/j.joca.2016.06.005
88. Tang Q, Zheng G, Feng Z, Tong M, Xu J, Hu Z, et al. Wogonoside inhibits IL-1β induced catabolism and hypertrophy in mouse chondrocyte and ameliorates murine osteoarthritis. Oncotarget. (2017) 8(37):61440–56. doi: 10.18632/oncotarget.18374
89. Cheng C, Zhang F-J, Tian J, Tu M, Xiong Y-L, Luo W, et al. Osteopontin inhibits HIF-2α mRNA expression in osteoarthritic chondrocytes. Exp Ther Med (2015) 9(6):2415–9. doi: 10.3892/etm.2015.2434
90. Wang P, Ye Y, Yuan W, Tan Y, Zhang S, Meng Q. Curcumin exerts a protective effect on murine knee chondrocytes treated with IL-1β through blocking the NF-κB/HIF-2α signaling pathway. Ann Transl Med (2021) 9(11):940. doi: 10.21037/atm-21-2701
91. Jhun JY, Na HS, Shin JW, Jung KA, Seo HB, Ryu JY, et al. Notoginseng radix and rehmanniae radix preparata extract combination (YH23537) reduces pain and cartilage degeneration in rats with monosodium iodoacetate-induced osteoarthritis. J Med Food (2018) 21(8):745–54. doi: 10.1089/jmf.2017.4041
92. Murahashi Y, Yano F, Kobayashi H, Makii Y, Iba K, Yamashita T, et al. Intra-articular administration of IκBα kinase inhibitor suppresses mouse knee osteoarthritis via downregulation of the NF-κB/HIF-2α axis. Sci Rep (2018) 8(1):16475. doi: 10.1038/s41598-018-34830-9
93. Choi M-C, Choi WH. Mithramycin a alleviates osteoarthritic cartilage destruction by inhibiting HIF-2α expression. Int J Mol Sci (2018) 19(5):1411. doi: 10.3390/ijms19051411
94. Hwang HS, Park SJ, Lee MH, Kim HA. MicroRNA-365 regulates IL-1β-induced catabolic factor expression by targeting HIF-2α in primary chondrocytes. Sci Rep (2017) 7(1):17889. doi: 10.1038/s41598-017-18059-6
95. Moon SJ, Woo YJ, Jeong JH, Park MK, Oh HJ, Park JS, et al. Rebamipide attenuates pain severity and cartilage degeneration in a rat model of osteoarthritis by downregulating oxidative damage and catabolic activity in chondrocytes. Osteoarthritis Cartilage. (2012) 20(11):1426–38. doi: 10.1016/j.joca.2012.08.002
96. Kim HE, Rhee J, Park S, Yang J, Chun JS. Upregulation of atrogin-1/FBXO32 is not necessary for cartilage destruction in mouse models of osteoarthritis. Osteoarthritis Cartilage. (2017) 25(3):397–400. doi: 10.1016/j.joca.2016.07.008
97. Oh H, Kwak JS, Yang S, Gong MK, Kim JH, Rhee J, et al. Reciprocal regulation by hypoxia-inducible factor-2α and the NAMPT-NAD(+)-SIRT axis in articular chondrocytes is involved in osteoarthritis. Osteoarthritis Cartilage. (2015) 23(12):2288–96. doi: 10.1016/j.joca.2015.07.009
98. Ishizuka S, Sakai T, Hiraiwa H, Hamada T, Knudson W, Omachi T, et al. Hypoxia-inducible factor-2α induces expression of type X collagen and matrix metalloproteinases 13 in osteoarthritic meniscal cells. Inflammation Res (2016) 65(6):439–48. doi: 10.1007/s00011-016-0926-1
99. Bouvard B, Abed E, Yéléhé-Okouma M, Bianchi A, Mainard D, Netter P, et al. Hypoxia and vitamin d differently contribute to leptin and dickkopf-related protein 2 production in human osteoarthritic subchondral bone osteoblasts. Arthritis Res Ther (2014) 16(5):459. doi: 10.1186/s13075-014-0459-3
100. Yang S, Ryu J-H, Oh H, Jeon J, Kwak J-S, Kim J-H, et al. NAMPT (visfatin), a direct target of hypoxia-inducible factor-2α, is an essential catabolic regulator of osteoarthritis. Ann Rheum Dis (2015) 74(3):595–602. doi: 10.1136/annrheumdis-2013-204355
101. Khan WS, Adesida AB, Hardingham TE. Hypoxic conditions increase hypoxia-inducible transcription factor 2alpha and enhance chondrogenesis in stem cells from the infrapatellar fat pad of osteoarthritis patients. Arthritis Res Ther (2007) 9(3):R55. doi: 10.1186/ar2211
102. Chen L, Wang Y, Li S, Zhou W, Sun L. High expression of NDRG3 in osteoarthritis patients. Arthroplasty. (2021) 3(1):1. doi: 10.1186/s42836-020-00064-2
103. Qin N, Wei L, Li W, Yang W, Cai L, Qian Z, et al. Local intra-articular injection of resveratrol delays cartilage degeneration in C57BL/6 mice by inducing autophagy via AMPK/mTOR pathway. J Pharmacol Sci (2017) 134(3):166–74. doi: 10.1016/j.jphs.2017.06.002
104. Weng T, Xie Y, Yi L, Huang J, Luo F, Du X, et al. Loss of vhl in cartilage accelerated the progression of age-associated and surgically induced murine osteoarthritis. Osteoarthritis Cartilage. (2014) 22(8):1197–205. doi: 10.1016/j.joca.2014.06.031
105. Li Z, Meng D, Li G, Xu J, Tian K, Li Y. Overexpression of microRNA-210 promotes chondrocyte proliferation and extracellular matrix deposition by targeting HIF-3α in osteoarthritis. Mol Med Rep (2016) 13(3):2769–76. doi: 10.3892/mmr.2016.4878
106. Yang M, Yan X, Yuan F-Z, Ye J, Du M-Z, Mao Z-M, et al. MicroRNA-210-3p promotes chondrogenic differentiation and inhibits adipogenic differentiation correlated with HIF-3 signalling in bone marrow mesenchymal stem cells. BioMed Res Int (2021) 2021:6699910. doi: 10.1155/2021/6699910
107. Kovács B, Vajda E, Nagy EE. Regulatory effects and interactions of the wnt and OPG-RANKL-RANK signaling at the bone-cartilage interface in osteoarthritis. Int J Mol Sci (2019) 20(18):4653. doi: 10.3390/ijms20184653
108. Hirata M, Kugimiya F, Fukai A, Saito T, Yano F, Ikeda T, et al. C/EBPβ and RUNX2 cooperate to degrade cartilage with MMP-13 as the target and HIF-2α as the inducer in chondrocytes. Hum Mol Genet (2012) 21(5):1111–23. doi: 10.1093/hmg/ddr540
109. Wang P, Xiong X, Zhang J, Qin S, Wang W, Liu Z. Icariin increases chondrocyte vitality by promoting hypoxia-inducible factor-1α expression and anaerobic glycolysis. Knee. (2020) 27(1):18–25. doi: 10.1016/j.knee.2019.09.012
110. Huang Z, Zhou M, Wang Q, Zhu M, Chen S, Li H. Mechanical and hypoxia stress can cause chondrocytes apoptosis through over-activation of endoplasmic reticulum stress. Arch Oral Biol (2017) 84:125–32. doi: 10.1016/j.archoralbio.2017.09.021
111. Markway BD, Cho H, Zilberman-Rudenko J, Holden P, McAlinden A, Johnstone B. Hypoxia-inducible factor 3-alpha expression is associated with the stable chondrocyte phenotype. J Orthop Res (2015) 33(11):1561–70. doi: 10.1002/jor.22930
112. Xiaoshi J, Maoquan L, Jiwei W, Jinqiu N, Ke Z. SETD7 mediates the vascular invasion in articular cartilage and chondrocytes apoptosis in osteoarthriis. FASEB J (2021) 35(3):e21283. doi: 10.1096/fj.202000373RRRR
113. Song J, Kang Y-H, Yoon S, Chun C-H, Jin E-J. HIF-1α:CRAT:miR-144-3p axis dysregulation promotes osteoarthritis chondrocyte apoptosis and VLCFA accumulation. Oncotarget. (2017) 8(41):69351–61. doi: 10.18632/oncotarget.20615
114. del Rey MJ, Izquierdo E, Caja S, Usategui A, Santiago B, Galindo M, et al. Human inflammatory synovial fibroblasts induce enhanced myeloid cell recruitment and angiogenesis through a hypoxia-inducible transcription factor 1alpha/vascular endothelial growth factor-mediated pathway in immunodeficient mice. Arthritis Rheumatol (2009) 60(10):2926–34. doi: 10.1002/art.24844
115. Zhang H, Ding L, Shi X, Mei W, Huang Z, Zhang L, et al. Imperatorin alleviated NLR family pyrin domain-containing 3 inflammasome cascade-induced synovial fibrosis and synovitis in rats with knee osteoarthritis. Bioengineered. (2021) 12(2):12954–64. doi: 10.1080/21655979.2021.2012949
116. Wang L, Wang Z, Liu Q, Su J, Wang T, Li T. Effect of whole body vibration on HIF-2α expression in SD rats with early knee osteoarthritis. J Bone Miner Metab (2020) 38(4):491–500. doi: 10.1007/s00774-020-01092-3
117. Coimbra IB, Jimenez SA, Hawkins DF, Piera-Velazquez S, Stokes DG. Hypoxia inducible factor-1 alpha expression in human normal and osteoarthritic chondrocytes. Osteoarthritis Cartilage. (2004) 12(4):336–45. doi: 10.1016/j.joca.2003.12.005
118. Im S, Kim D-W. Nkx3.2 induces oxygen concentration-independent and lysosome-dependent degradation of HIF-1α to modulate hypoxic responses in chondrocytes. Cell Signal (2017) 36:127–38. doi: 10.1016/j.cellsig.2017.05.001
Keywords: osteoarthritis, HIFs, degradation of extracellular matrix, apoptosis, autophagy, inflammatory reaction
Citation: Zhang X-A and Kong H (2023) Mechanism of HIFs in osteoarthritis. Front. Immunol. 14:1168799. doi: 10.3389/fimmu.2023.1168799
Received: 18 February 2023; Accepted: 09 March 2023;
Published: 20 March 2023.
Edited by:
Yufeng Yao, Huazhong University of Science and Technology, ChinaReviewed by:
Yubao Ma, Beijing Rehabilitation Hospital, Capital Medical University, ChinaHongsong Zhang, Nanjing Medical University, China
Copyright © 2023 Zhang and Kong. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Xin-An Zhang, zhangxa2725@163.com