Shuo Wang
Hanming Yu
Shi Liu- Department of Pulmonary and Critical Care Medicine, The Fourth Affiliated Hospital of China Medical University, Shenyang, China
Pulmonary fibrosis (PF) is a highly complex and challenging disease affecting the respiratory system. Patients with PF usually have an abbreviated survival period and a consequential high mortality rate after the diagnosis is confirmed, posing serious threats to human health. In clinical practice, PF is typically treated by antifibrotic agents, such as Pirfenidone and Nintedanib. However, these agents have been reported to correlate with substantial adverse effects, escalating costs, and insufficient efficacy. Moreover, it remains unclarified about the multifactorial pathology of PF. Therefore, there is an urgent demand for elucidating these underlying mechanisms and identifying safe, efficient, and targeted therapeutic strategies for PF treatment. The crucial role of the transforming growth factor-β (TGF-β) signaling pathway in PF development has been explored in many studies. MicroRNAs (miRNAs), which function as post-transcriptional regulators of gene expression, can significantly affect the development of PF by modulating TGF-β signaling. In turn, TGF-β signaling can regulate the expression and biogenesis of miRNAs, thereby substantially affecting the progression of PF. Hence, the therapeutic strategies that focus on the drug-targeted regulation of miRNAs, either by augmenting down-regulated miRNAs or inhibiting overexpressed miRNAs, may hinder the pathways related to TGF-β signaling. These strategies may contribute to the prevention and suppression of PF progression and may provide novel insights into the treatment of this disease.
1 Introduction
Pulmonary fibrosis (PF) encapsulates a range of persistent and progressively deteriorating lung disorders that incrementally affects the interstitium. This disease may induce hampered gas exchange, breathlessness, and compromised quality of life, ultimately resulting in respiratory failure and death (1). As the most prevalent subtype of PF, idiopathic pulmonary fibrosis (IPF) is an chronic, progressive, and fibrotic disorder in the interstitial lung (2). Globally, the estimated incidence of IPF ranges from 0.09 and 1.30 per 10,000 individuals, while the average age of patients with IPF is approximately 65–70 years, presenting a significantly higher incidence with an increase in age (3). In the context of the aging population worldwide, the burden of PF on patients and healthcare systems is predicted to rise progressively. According to current treatment guidelines, Pirfenidone and Nintedanib are recommended in the treatment of PF (4). However, the efficacy of these agents in decelerating disease progression and enhancing the quality of life is limited to a certain extent. Additionally, they are often associated with gastrointestinal tolerability concerns (5–7). Therefore, the development of novel drug therapies is of paramount importance for the treatment of this disease.
IPF is characterized by the excessive production and disorganized deposition of extracellular matrix (ECM) components, resulting in irreversible structural distortions and loss of organ function (8). It is now widely recognized that IPF arises from a complex interplay of genetic and environmental risk factors, with repetitive localized microinjuries to the senescent alveolar epithelium playing a central role. These micro-injuries initiate aberrant epithelial–fibroblast communication, the induction of matrix-producing myofibroblasts, and considerable extracellular matrix accumulation and remodelling of lung interstitium (2).
Transforming growth factor-β (TGF-β) is a pivotal mediator in fibrogenesis (9, 10). There are three TGF-β isoforms (TGF-β1, β2, and β3), alongside three cell-surface receptors - Type I (TGFBR1), Type II (TGFBRI2), and Type III (TGFBR3), all of which contribute to the TGF-β signaling pathway (11). Triggered by the ligand-receptor interaction (9), TGF-β signaling may be initiated when TGF-β first binds to its specific receptor, TGFBR2, thereby recruiting TGFBR1 into the complex via the unique interface generated by the TGF-β-TGFBR2 complex. This forms a heterotetramer complex consisting of a single dimeric TGF-β molecule binding to two TGFBR1 molecules and two TGFBR2 molecules. The formation of this complex leads to the phosphorylation of TGFBR1 by TGFBR2, which subsequently phosphorylates Smad proteins to propagate signals to the nucleus, bind to consensus sequences, and regulate gene transcription (11). As a co-receptor, TGFBR3 promotes the binding of ligands to TGFBR2, which augments TGF-β signaling (12). As the downstream components of SMAD signaling, Smad2/Smad3 are hypothesized to be paramount intermediators of TGF-β signaling in tissue fibrogenesis. Smad4 can work synergistically with Smad2/3 to facilitate this process, while Smad6 and Smad7 can function as negative regulators to mitigate TGF-β-mediated fibrosis (13). Apart from initializing Smad-dependent signaling chains, TGF-β can instigate Smad-independent signaling cascades, including the MAPK family (Erk (14, 15), JNK (16, 17), and p38 MAPK (18, 19)), Rho-like GTPases (20, 21), and the AKT/phosphatidylinositol-3 kinase pathway (22, 23). IPF is a disease primarily associated with aging, and elevated TGF-β1 is a major factor in its pathogenesis (24). TGF-β is released following epithelial cell injury and serves as a central pro-fibrotic growth factor driving the progression of pulmonary fibrosis. Its multifunctional roles include stimulating the proliferation and differentiation of epithelial cells and fibroblasts, activating ECM production in myofibroblasts, catalyzing epithelial-mesenchymal transition, accelerating epithelial apoptosis and cell migration, and inducing the production of connective tissue growth factor (CTGF) along with other mediators such as Fibroblast Growth Factor (FGF), Insulin-like Growth Factor (IGF), and Platelet-Derived Growth Factor (PDGF) (25).The heightened level of TGF-β1 has been observed in both animal models of IPF and tissue samples from IPF patients (26). The overexpression of active TGF-β1 may result in the progression of PF (27), whereas inhibiting TGF-β signaling can mitigate PF in animal models (28).
MicroRNAs (miRNAs) are a highly conserved group of small single-stranded non-coding RNAs measuring between 19 to 25 nucleotides. They can modulate genes at both the transcriptional and post-transcriptional levels by binding to the 3′-untranslated region (UTR) of target mRNAs (29, 30). In animals, miRNA gene transcription, facilitated by RNA polymerase II (pol II), first yields extended primary transcripts (pri-miRNAs). These pri-miRNAs are subsequently cropped by the RNase-III enzyme Drosha to produce hairpin intermediates (pre-miRNAs) located within the nucleus. Drosha can be fused with its indispensable cofactor DGCR8/Pasha into a large ensemble (500-650 kDa) named the microprocessor complex (31). DGCR8/Pasha, accounting for approximately 120 kDa in size, is equipped with two dsRNA-binding structural domains. Thereafter, the pre-miRNA is shuttled into the cytoplasm through exportin-5, a constituent of the Ran-dependent nuclear transporter receptor family. Upon reaching the cytoplasm, pre-miRNAs are finally processed into approximately 22-nucleotide miRNA duplexes by the cytoplasmic RNase-III protein Dicer, but their cellular persistence is typically transient. Typically, one strand of this transient duplex would degrade while the other would transform into the mature miRNA. The strand choice for retention is determined by the relative thermodynamic stability of both ends of the duplex (32). Dicer, a cog in the miRNA machinery, is known to form interactions with a variety of proteins, each imparting different functions in miRNA stability, effector complex formation, and operational actions. For instance, human AGO2, a member of the Argonaute protein family, has been recently validated to function as a “slicer” enzyme, which can cleave target mRNAs (33, 34).
Mature miRNAs are sorted into exosomes or microvesicles (35), and extracellular miRNAs can also be loaded into high-density lipoproteins (HDL) (36, 37) or bound to AGO2 proteins outside of vesicles (38). These three mechanisms protect miRNAs from degradation and ensure their stability. Given the transporter capability of vesicles, the role of miRNAs in exosomes has garnered increasing attention. Since exosomal miRNAs can stably persist in the blood, urine, and other body fluids of patients, exosomes can reflect their tissue or cellular origin through the presence of specific surface proteins. The use of exosomes and their cargo miRNAs as clinical tools for diagnosing and monitoring diseases holds substantial promise and may even be beneficial for gene therapy in certain conditions.It has been shown that HDL can deliver miRNAs to recipient cells and alter gene expression. For example, HDL delivery of miR-223 significantly reduced EFNA1 and RhoB mRNA levels in hepatocytes (36). Manipulation of HDL-miRNA levels and the use of HDL as a delivery vehicle for RNA and chemicals have demonstrated potential in the treatment of cardiovascular disease. HDL-miR-223 mimic approaches can be used to prevent or treat hypercholesterolemia (hepatic cholesterol biosynthesis) and endothelial activation (monocyte and neutrophil adhesion) and attenuate atherosclerosis (39).
It has been recently revealed that there is a strong association between numerous miRNAs and tissue or organ fibrogenesis (40–43). Promising results have been elicited from miRNA mimics and miRNA inhibitors, and they are expected to become novel therapeutic agents, which are currently under preclinical development (44). KADOTA et al. corroborated the antifibrotic properties of miR-16, miR-26a, miR-26b, miR-141, miR-148a, and miR-200a located in human bronchial epithelial cell-derived extracellular vesicles (HBEC EVs). They further proposed that the introduction of these HBEC EVs may hold promise as an antifibrotic strategy in the treatment of IPF through miRNA-mediated curbs on TGF-β signaling (45).
2 The interaction between TGF-β signaling and MiRNAs
TGF-β signaling can exert impacts on the expression of miRNAs while concurrently being regulated by these miRNAs. Moreover, a majority of the classical TGF-β signaling pathway constituents may be susceptible to miRNA impacts. Specifically, miR-424 enhances profibrotic properties via stimulating the TGF-β/Smad pathway, which can be attributed to the direct engagement with TGIF2, an intrinsic repressor of TGF-β signaling. This further results in sub-mucosal fibrosis within the oral mucosa (46). On the contrary, miR-130a also presents antifibrotic properties by modulating the expression of TGFBR1 via directly targeting TGFBR1, thus inhibiting cardiac fibrosis after myocardial infarction (47). Additionally, miR-326 is validated to correlate with TGF-β1 3’UTR, which inhibits the expression of TGF-β1 at the post-transcriptional stage, thereby mitigating PF (48).
Furthermore, the molecules involved in TGF-β signaling are capable of modulating the expression and biogenesis of miRNAs. The biogenesis of miRNAs encompasses synchronized processes, including miRNA transcription and the consequent processing and maturation of miRNA units. Davis et al. uncovered that TGF-β signaling enhanced the processing of the primary transcript of miR-21 (pri-miR-21) into the precursor miR-21 (pre-miR-21) through the DROSHA complex (49). Receptor-activated Smad (R-Smad) proteins that are exclusive to TGF-β signaling are enlisted to the RNA deconjugating enzyme p68 complex (also termed DDX5) of the ‘pri-miR-21’, where they facilitate the maturation of miRNAs by managing DROSHA, which is a constituent of the DROSHA microprocessor complex.
Marquez et al. reported a unique positive feedback loop, in which TGF-β stimulated the processing of the primary miR-21 precursor (pri-miRNA) into mature miR-21 (50). Interestingly, the mature miR-21 suppressed TGF-β signaling, but the R-Smad protein was also conscripted to the primiR-21 RNA deconjugating enzyme p68 complex. The suppression of SMAD7, a TGF-β signaling inhibitor, can be induced by mature miR-21, thereby facilitating fibrosis. It has been confirmed in numerous studies that the expression of various miRNAs can be altered in different cell types after the treatment with TGF-β family ligands. For example, Ottaviani et al. found that TGF-β incited the lncRNA MIR100HG through SMAD2/3 transcription, which housed miR-100, miR-125b, and let-7a within its intron (51). Additionally, Yang et al. observed that miR1306 negatively influenced TGF-β/Smad3 signaling by targeting TGFBR2 (52). In contrast, SMAD4 was directly associated with the miR-1306 promoter, thereby inhibiting its transcriptional activity.
The connection between TGF-β signaling and miRNA mechanisms has been proved in many studies. In this review, the acting patterns of this interaction and their functions in the occurrence and progression of PF are summarized. This interaction is illustrated in the following Figure 1.
Figure 1. This schema elucidates the role of miRNAs that modulate the pivotal molecules involved in the TGF-β signaling pathway in PF. Likewise, the central molecules of the TGF-β signaling pathway have interactive roles in regulating miRNA expression and biogenesis. Emphasizing the presence of feedback loops, miRNAs involved in forming negative and positive feedback with the TGF-β signaling pathway are specifically highlighted in different colors. Specifically, blue represents negative feedback loops, whereas red represents positive feedback pathways.
3 MiRNAs impeding the progression of PF
3.1 MiR-133a
MiR-133a is mainly expressed in muscle tissues (53) predominantly conserved in skeletal and cardiac muscles. It plays a critical role in various physiological processes, such as fibrosis (54, 55), myocardial infarction (56), scarring (57), cancer (58), and bone metabolism (59). It has been recently revealed that the expression of miR-133a is considerably down-regulated in the lungs of patients with IPF compared with age-matched males without fibrotic lung diseases (60). Wei et al. unveiled a novel role of miR-133a as a negative feedback regulator in the profibrotic signaling pathway of TGF-β1 (55). MiR-133a can impede the differentiation of myofibroblasts by targeting multiple constituents of the profibrotic pathway of TGF-β1, including TGFBR1, CTGF, and collagen type 1-alpha1 (Col1a1). Besides, TGF-β1 promotes the transcription of miR-133a through the activation of both conventional (Smad3) and unconventional (p38MAPK) signaling pathways. This instigates a negative feedback loop, thereby inhibiting the progression of PF. Intriguingly, the overexpression of miR-133a has been found to alleviate PF induced by bleomycin in mice, underscoring its potential therapeutic utility (55) (Table 1).
Table 1. Impact of miRNAs in pulmonary fibrosis.
3.2 MiR-29
The miRNA-29 family, including miR-29a, miR-29b, and miR-29c, has been confirmed to have a pivotal role in the fibrosis process within several organs, thus, garnering interest as a potential antifibrotic regulator (61). CUSHING et al. reported a negative correlation of the level of miR-29 with the expression of profibrotic genes and the severity of fibrosis. In IMR-90 cells, a fetal lung fibroblast cell line commonly utilized in fibrosis molecular mechanism studies, miR-29 is suppressed by TGF-β, and many fibrosis-related genes normally up-regulated by TGF-β are derepressed after the knockdown of miR-29. Remarkably, it has been demonstrated in a comparative analysis between TGF-β and miR-29 targets that miR-29 can independently regulate different subsets of profibrotic genes, such as laminin, integrins, ADAMTS9, ADAM12, NID1 gene, and integrin ITGA11 (62). Xiao et al. found that miR-29 was negatively regulated by TGF-β/Smad signaling during fibrosis, with Smad3 identified as a downstream target. Notably, the overexpression of miR-29 could inversely regulate the expression of TGF-β, connective tissue growth factors (CTGFs), and Smad3 signaling. Importantly, non-invasive miR-29 gene therapies based on the SB transposon system have been developed for the treatment of PF. These therapies could enhance the expression of miR-29 in normal mouse lungs to prevent bleomycin-induced fibrosis. Besides, they can also significantly restore the higher level of miR-29 in fibrotic lungs, thus avoiding the progression of PF in mouse models (63). Chioccioli et al. uncovered that the decreased level of miR-29 in the peripheral blood of IPF patients was correlated with the poor prognosis and significantly decreased survival rate of these patients (64). Astonishingly, the supplementation with the miR-29 mimic, MRG-229, can mitigate the up-regulation of fibrosis-associated genes instigated by TGF-β and inhibit the synthesis and secretion of collagen in both standard and IPF cells in vitro. Moreover, similar outcomes are also observed in bleomycin-induced PF rats and non-human primate models, indicating an improvement in fibrosis. These findings may support the exploration of miR-29 as an innovative and potentially effective therapy for lung diseases characterized by fibrosis.
Interestingly, IPF is characterized by the progression from the periphery toward the center. This disease presents distinct pathological characteristics in different lung regions that may resemble varying stages of the disease, hence it can be considered a heterogeneous and progressive disease (65).
McDonough et al. demonstrated that the expression of many collagen genes in the lungs of IPF patients, least affected by the disease, was up-regulated significantly before observable changes in protein levels. Simultaneously, a decrease in the miRNA level of miR-29 was also observed at this stage, implying that IPF patients, even with normal histology, may exhibit molecular abnormalities (66). These findings may potentially assist in implementing more effective diagnostic measures or tailoring more efficient therapies for patients with PF.
3.3 MiR-130a-3p
The close association between miR-130a-3p and fibrosis across various tissues has been reported in many studies. Specifically, miR-130a-3p can bind to MAPK1, TGFBR1, and TGFBR2 and inhibit their expression, a mechanism that contributes to alleviating hepatic fibrosis (67). However, in the context of obstructive nephropathy, miR-130a-3p directly targets the 3’-UTR of SnoN to suppress the expression of SnoN, thereby inadvertently promoting the activation of TGF-β1/Smad signaling related to renal fibrosis (68). The correlation of miR-130a-3p with lung inflammation (69) and airway remodeling (70) has been demonstrated in some studies. In the previous, TGFBR2 was identified as a potential target of miR-130a-3p. Besides, the interaction of miR-130a-3p/TGFBR2 axis can inhibit the differentiation of lung fibroblasts via the TGF-β1/Smad signaling pathway. Additionally, it has been found that the down-regulated expression of miR-130a-3p can affect the secretion of inflammatory cytokines (including IL-1β, IL-6, TNF-α, and TGF-β1) in the inflammatory and fibrosis phases and the deposition of the extracellular matrix (α-SMA, FN, HYP, and collagen). Overall, these findings suggest that miR-130a-3p can exert anti-inflammatory and antifibrotic effects in the treatment of PF (71, 72).
3.4 MiR-200
Among vertebrates, the miR-200 family is deemed one of the most conserved miRNAs, encompassing five members: miR-200a, miR-200b, miR-200c, miR-141, and miR-429. This family holds a central role in establishing epithelial phenotypes during embryogenesis and organogenesis (64). Yang unraveled the significant down-regulated expression of miR-200a, miR-200b, and miR-200c in the lungs of mice affected by experimental PF. Concurrently, the expression of miR-200a and miR-200c was down-regulated in the lungs of IPF patients. Interestingly, it was validated that the members of the miR-200 family were inversely correlated with the TGF-β1-induced EMT, and miR-200c even demonstrated the ability to attenuate PF in mice (73). As revealed in recent studies, miR-200a exhibits an antifibrotic effect by inhibiting the profibrotic TGF-β/SMAD-3/α-SMA pathway (74). Moreover, the expression of ZEB1 is up-regulated by the TGF-β pathway in IPF. Hence, it can be speculated that miR-200 s can potentially govern the EMT in IPF by targeting and suppressing ZEB1 and ZEB2/SIP1 (75). These findings could pave the way for future therapeutic strategies targeting miR-200 s in the treatment of IPF.
3.5 MiR-9-5p
The dysregulation of miR-9-5p has been found to correlate with fibrosis in various tissues and organs (76–78). It has been corroborated that the expression of miR-9-5p is down-regulated in PF tissues compared with normal physiological conditions. Interestingly, the overexpression of miR-9-5p has been found to suppress the expression of TGF-β1 and p-Smad2 (79). Recently, Fierro et al. identified a feedback loop between TGF-β1 and miR-9-5p, demonstrating an intriguing interaction. They found that TGF-β1 up-regulated the expression of miR-9-5p through a mechanism dependent on reactive oxygen species (ROS), while miR-9-5p was found to negatively regulate the TGF-β signaling pathway by targeting TGFBR2 and NADPH oxidase 4 (NOX4). These data prove that miR-9-5p exerts antifibrotic effects in a bleomycin-induced PF animal model. Notably, miR-9-5p delays the TGF-β1-dependent transformation of lung fibroblasts into myofibroblasts by inhibiting the phosphorylation of Smad2 and the nuclear translocation of Smad2/3 (80). These findings highlight the complex and dynamic interplay of miR-9-5p in the modulation of fibrosis, offering an intriguing target for the therapeutic intervention of PF.
3.6 MiR-26a
MiR-26a has been reported to play an important role in the regulation of many diseases, such as renal tubulointerstitial fibrosis, lens fibrosis, and cataract (81, 82). MiR-26a can regulate the expression of let-7d by targeting Lin28B, which contributes to the regulatory effect of miR-26a on EMT, and ultimately, may enhance the anti IPF This could help miR-26a to regulate EMT and ultimately enhance the anti-fibrotic activity of miR-26a against IPF (83). LIANG found that overexpression of miR-26a inhibited TGF-β1-induced fibrosis in MRC-5 cells and attenuated experimental pulmonary fibrosis in mice. More importantly, the positive feedback loop between miR-26a and p-Smad3 was associated with pulmonary fibrosis. TGF-β1 negatively regulated miR-26a expression by regulating Smad3, and miR-26a inhibited the nuclear translocation of p-Smad3 in order to block signaling events downstream of TGF-β1, which ultimately attenuated collagen deposition and mitigated pulmonary fibrosis (84).
4 MiRNAs facilitating the progression of PF
4.1 MiR-21
MiR-21 has been implicated in an array of lung diseases, including acute lung injury/acute respiratory distress syndrome (85), asthma (86), PF (87), and lung cancer (88). An increase in the expression level of miR-21 has been documented in both the PF mouse model (in the bleomycin model) and tissue samples in IPF patients (89, 90). Similarly, Zhou et al. observed that TGF-β1 induced the expression of miR-21 upon the interaction with TGFBR1 through the binding of SMAD3 or SMAD2/3/4 complexes to the miR-21 promoter region. This process culminates with the promotion of ECM protein deposition in both human lung fibroblasts IMR-90 and a mouse model related to bleomycin-induced PF. This implies a novel molecular mechanism working via the positive feedback axis of TGFβ1/SMADs/miR-21 (91).
Sato et al. analyzed the influence of TGF-β1 and tissue stiffness on the expression of miR-21 in rat lung fibrocytes and human circulating fibrocytes. They found that fibrocytes treated with varying concentrations of TGF-β1 and cultured on plates exhibited different levels of stiffness. Fibrocytes were cultivated on soft (1 kPa) plates to simulate the characteristics of normal pulmonary tissue as well as on stiff (50 kPa) plates to replicate the conditions in fibrotic lung tissues. Interestingly, the substrate stiffness changes miR-21 expression in fibrocytes. Culturing lung fibrocytes on hard plates increased miR-21 expression compared to culturing lung fibrocytes on soft plates (92).
Radiation-induced lung fibrosis (RILF) is one of the most severe side effects of lung cancer radiotherapy on normal tissues. It poses a considerable challenge to the broader application of radiotherapy in treating lung cancer patients (93, 94). It has been revealed that the expression of miR-21 is significantly up-regulated in regions affected by radiation injury. Concomitantly, miR-21 has been found to down-regulate the expression of Smad7 while amplifying the phosphorylation of Smad2. This, in turn, propels the activation of Smad-dependent TGF-β signaling, a noteworthy contributor to the onset of RILF. Hence, the targeted mitigation of miR-21 in the affected regions may hold potential as an effective therapeutic strategy in preventing the progression of RILF (95).
4.2 MiR-145
MiR-145 is highly expressed in blastomeres, which constitute a collection of pluripotent stem cells. The primary function of miR-145 is to inhibit the self-renewal of embryonic stem cells (ESCs), thereby inducing lineage-specific differentiation. Specifically, miR-145 has been observed to reprogram fibroblasts into smooth muscle cells during development (96–98). As reported in recent studies, patients with COVID-19 and IPF may exhibit the mutual up-regulation of miRNAs, including miR-145-5p, which may play a role in the progression of PF (99). Yang et al. identified that the level of the primary transcript of the miR-145 cluster gene (pri-miR-145) increased in TGF-β1-treated lung fibroblasts. This implied that the up-regulated expression of mature miR-145 may be attributed to the enhanced transcription of the miR-145 gene cluster. Besides, they also confirmed that miR-145 played a pivotal role in promoting the progression of PF by reinforcing the activation of latent TGF-β1. MiR-145 can fulfill this function by up-regulating the expression of α-SMA, thereby boosting the contractility of myofibroblasts. Intriguingly, the mechanical forces presented by cell contraction can act as a trigger to activate latent TGF-β1. It has further been observed that the knockout of miR-145 protected mice from bleomycin-induced PF, suggesting that miR-145 could be targeted as a potential treatment strategy for resisting pathological fibrotic diseases (100).
4.3 MiR-155
As a principal miRNA, miR-155 has been validated to play a pivotal role in the development of fibrosis, with persistent up-regulated expression observed across various fibrotic diseases (101). Notably, miR-155 has been confirmed to enhance collagen synthesis in animal models related to fibrosis and in human fibroblast cell lines derived from fibrotic tissues, thus exacerbating fibrosis. Further, it has been identified that miR-155 is instrumental in the activation of TGF-β1 in fibroblasts and macrophages, offering a potential alternative target for the treatment of fibrotic lesions (102). Kong et al. demonstrated that the TGF-β/Smad4 pathway incited the activity and expression of the miR-155 promoter. This, in turn, stimulates the TGF-β-induced EMT and the dissolution of tight junctions, as well as encouraging cell migration and invasion (103). Sun et al. unraveled that using a miR-155 antagonist could significantly mitigate histological changes and decrease hydroxyproline levels in a mouse model related to bleomycin-induced PF. The inhibition of miR-155 can down-regulate the expression of IL-4, TGF-β, and interferon-γ after BLM treatment. It was further observed that the mitogen-activated protein kinase signaling pathway of TGF-β-activated kinase 1/MAPK 7 (MAP3K7)-binding protein 2 (TAB2) was activated by BLM. However, this process could be suppressed by the miR-155 antagonist. The in vivo application of the antagomir-155 can mitigate BLM-induced pathological changes and may, therefore, represent a promising therapeutic strategy for PF (104).
Due to the central role of miRNAs in the immune system, miR-155-5p is intimately involved in the inflammatory response. Capsaicin (Cap) quenched the inflammatory response in a rat model of bleomycin-induced PF by interrupting the IL-1β, TNF-α, and TGF-β1 pathways through down-regulating the expression of miR-155-5p. Hence, IPF-related lung injury may be ameliorated by regulating the expression of miR-155 (105).
4.4 MiR-424
MiR-424-5p has been validated to correlate with the occurrence, progression, treatment, and prognosis of tumors, embodying either the role of an oncogene or a tumor suppressor gene (106–108). The results of recent studies have provided novel insights into the function of miR-424 in the landscape of PF. The elevated level of miR-424 has been detected in the extracellular vesicles of lung fibroblasts originating from IPF patients (109). Moreover, a 1.7-fold increase in miR-424 expression was also observed in human fibrotic lung tissues, and a notable 2.6-fold increase was documented in TGF-β1-treated HLFs, compared with non-fibrotic lung tissues. MiR-424 can exert profibrotic effects by targeting the expression of Slit2, a prohibitive regulator that can curb profibrotic signaling of TGF-β1 and function as an inhibitor of the TGF-β1 signaling pathway (110). Xiao revealed that TGF-β propagated the expression of miR-424, which in turn suppressed Smurf2, a negative regulator of TGF-β signaling. Intriguingly, the silencing of Smurf2 by miR-424 augmented the activity of Smad3, thereby cementing the significance of miR-424 in TGF-β signaling. Overall, miR-424 orchestrates a positive feedback loop in the TGF-β signaling pathway, which promotes the differentiation of myofibroblasts in IPF (111).
4.5 MiR-182-5p
MiR-182-5p is markedly over-expressed in the lung tissues of mice suffering from BLM-induced fibrosis. TGF-β1 is a protein with known profibrotic effects, and it can induce the over-expression of miR-182-5p. Interestingly, miR-182-5p plays a role in the down-regulation of Smad7, which is specifically targeted by miR-182-5p, and this negative regulation results in the exacerbation of PF (112). As a major checkpoint in the TGF-β1/Smad signaling pathway, Smad7 is a negative regulator that can inhibit the phosphorylation of Smad2/Smad3, thereby interrupting TGF-β1 signaling (113). More importantly, miR-182-5p forms a positive feedback loop, a mechanism that expedites the deterioration of PF. By diminishing the level of miR-182-5p, it was observed that PF was alleviated through the suppression of profibrotic proteins (namely, fibronectin, α-smooth muscle actin, and p-Smad2/p-Smad3) and the potentiation of Smad7. Remarkably, the concurrent inhibition of miR-182-5p and miR-23a-3p in vitro and in vivo resulted in a reversal of the progression of lipopolysaccharide-induced lung injury and fibrosis in MLE-12 cells and mice (114).
4.6 MiR-199a-5p
It has been shown that miR-199a-5p is significantly increased in the serum of IPF patients compared to healthy controls (115). MiR-199a-5p regulates autophagy and mediates mesenchymal stem cell (MSC) senescence in IPF patients by targeting the Sirt1/AMPK signaling pathway, inhibition of miR-199a-5p rejuvenated IPF-MSCs and increased their capacity to prevent lung fibrosis progression induced by bleomycin in mice (116). Lung fibroblasts overexpressing miR-199a-5p can increase SMAD4 expression, and miR-199a-5p can directly inhibit Caveolin-1 (CAV1 is a key effector of TGF-β signaling in lung fibroblasts) in lung fibroblasts, which can stimulate their proliferation, migration, invasion, and differentiation into myofibroblasts, thus promoting fibrotic (117).
5 Conclusion and perspective
TGF-β is a crucial instigator of pulmonary fibrogenesis and a principal mediator in the progression of PF. The activation of the TGF-β signaling pathway can catalyze the overexpression of profibrotic genes within the organism from various angles, culminating in fibrotic alterations within lung tissues. MiRNAs hold a pivotal role in the progression of PF. The existing findings underline the dual effects of miRNAs, suggesting that they can be utilized not only as diagnostic markers for PF but also as therapeutic targets for the treatment of diseases associated with PF. Of note, therapeutic miRNAs have been investigated in clinical trial stages (118). In the context of escalating disease severity, there are dramatic changes in the gene expression regulation patterns based on down-regulated miRNAs. The miR-29 family plays a dominant role in the early stages of PF, whereas the let-7 family takes precedence in the later stages of this disease (66).
In this comprehensive review, the intricate interplay between the TGF-β signaling mechanism and miRNAs in the progression of PF is elucidated. Antifibrotic miRNAs, such as miR-133a, miR-29, miR-130a-3p, miR-200, miR-9-5p and miR-26a, can inhibit the TGF-β signaling pathway and deter the progression of PF by acting on the positive regulators of signal transduction. Conversely, profibrotic miRNAs, such as miR-21, mir-145, miR-155, miR-424, miR-182-5p and miR-199a-5p, can enhance the TGF-β signaling pathway by repressing relevant negative regulators, thereby promoting the PF phenotype. Interestingly, there are also complex feedback regulatory loops. MiR-133a, miR-29, and miR-9-5p form a negative feedback loop with TGF-β-linked molecules, thus ameliorating PF. Simultaneously, miR-21, mir-145, miR-155, miR-424, and miR-182-5p generate a positive feedback loop with TGF-β-associated molecules, which promotes the progression of PF.
Many of the concerns about drugs with miRNAs are based on the fact that miRNA targeting has a broader and less specific mechanism that can easily lead to off-target effects compared to siRNA targeting, which has a high specificity. This factor is mainly due to incomplete binding at the 3’-UTR of the target sequence, especially at the seed region (119). Some miRNAs (within the same family) share a common seed region (bases 2–7 at the 5′ end), which is a key region for mRNA target recognition (120), and thus miRNA family members can target and repress the same genes. MiRNA therapeutics do not necessarily confine their effects to the intended tissues or cells, but they may also cause systemic side effects. For example, MRX34, a synthetic miR-34a mimic. MiR-34a not only acts as a tumor suppressor, but also affects immune cell signaling. MiR-34a is not only uptaken in tumor tissues, but also similarly uptaken in the bone marrow and the spleen, producing severe immune-associated side effects (121, 122).
Potential off-target effects and immunostimulation of miRNA-based drugs should be rigorously and extensively studied before application to animal models or human use. Overall, further unraveling the dynamic interaction between miRNAs via the TGF-β signaling pathway remains an indispensable trajectory for the development of novel antifibrotic treatment modalities.
Author contributions
SW: Writing – original draft, Writing – review & editing. HY: Writing – original draft. SL: Writing – original draft. YL: Writing – original draft. XG: Writing – review & editing.
Funding
The author(s) declare financial support was received for the research, authorship, and/or publication of this article. Liaoning Provincial Department of Education, General project, LJKZ0768, Mechanism of alveolar epithelial CFTR chloride channel in acute lung injury.
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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Keywords: transforming growth factor-β, MicroRNAs, pulmonary fibrosis, targeted therapy, feedback loop
Citation: Wang S, Yu H, Liu S, Liu Y and Gu X (2024) Regulation of idiopathic pulmonary fibrosis: a cross-talk between TGF-β signaling and MicroRNAs. Front. Med. 11:1415278. doi: 10.3389/fmed.2024.1415278
Edited by:
Alexandre Todorovic Fabro, University of São Paulo, BrazilReviewed by:
Akos Heinemann, Medical University of Graz, AustriaHong Xu, North China University of Science and Technology, China
Wagner Moneda Telini, Centro Universitário de Votuporanga, Brazil
Andrea Jazel Rodriguez Herrera, University of São Paulo, Brazil
Sabrina Batah, University of São Paulo, Brazil
Copyright © 2024 Wang, Yu, Liu, Liu and Gu. 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: Xiu Gu, eGl1Z3VAY211LmVkdS5jbg==