Yu Feng Shang
Yi Yang Shen1
Meng Chen Zhang
Tong Ying Wang
Xue Qun Chen
Jun Lin- 1Department of Stomatology, Key Laboratory of Oral Biomedical Research of Zhejiang Province, The First Affiliated Hospital, School of Medicine, Zhejiang University, Zhejiang University School of Stomatology, Hangzhou, China
- 2National Health Commission and Chinese Academy of Medical Sciences Key Laboratory of Medical Neurobiology, MOE Frontier Science Center for Brain Research and Brain Machine Integration, School of Brain Science and Brain Medicine, Zhejiang University, Hangzhou, China
- 3Department of Orthopedics, The Quzhou Affiliated Hospital of Wenzhou Medical University, Quzhou People’s Hospital, Quzhou, China
- 4Department of Neurobiology, Department of Neurology of the Second Affiliated Hospital, School of Brain Science and Brain Medicine, Hangzhou, China
The production and secretion of saliva is an essential function of the salivary glands. Saliva is a complicated liquid with different functions, including moistening, digestion, mineralization, lubrication, and mucosal protection. This review focuses on the mechanism and neural regulation of salivary secretion, and saliva is secreted in response to various stimuli, including odor, taste, vision, and mastication. The chemical and physical properties of saliva change dynamically during physiological and pathophysiological processes. Moreover, the central nervous system modulates salivary secretion and function via various neurotransmitters and neuroreceptors. Smell, vision, and taste have been investigated for the connection between salivation and brain function. The immune and endocrine functions of the salivary glands have been explored recently. Salivary glands play an essential role in innate and adaptive immunity and protection. Various immune cells such as B cells, T cells, macrophages, and dendritic cells, as well as immunoglobins like IgA and IgG have been found in salivary glands. Evidence supports the synthesis of corticosterone, testosterone, and melatonin in salivary glands. Saliva contains many potential biomarkers derived from epithelial cells, gingival crevicular fluid, and serum. High level of matrix metalloproteinases and cytokines are potential markers for oral carcinoma, infectious disease in the oral cavity, and systemic disease. Further research is required to monitor and predict potential salivary biomarkers for health and disease in clinical practice and precision medicine.
Introduction
The production and secretion of saliva are the typical functions of the salivary gland (SG). The SG is the first immune barrier in humans and animals, constantly facing external pathogens. Antibodies are known to be present in saliva, and salivary biomarkers are used to diagnose inflammation and antigen challenge, so SGs are considered to be potential immunization sites and useful proxies (1–5). The structure and function of SGs and the properties and composition of saliva, as well as other tissues in the oral cavity are summarized in Table 1 (1–23). SGs contain a variety of cells, including acinar, epithelial, immune, and endocrine cells. Saliva contains water, ions (Na+ and Ca2+), immunoglobulins, enzymes, mucins, and hormones. Besides, the more granular convoluted tubules in the submandibular glands produce cell growth factors in mice and rats (Table 1) (6).
Table 1 Cells, molecules, and microorganisms in oral tissue and saliva.
There are three bilateral salivary glands, the parotid (PG), submandibular (SMG), and sublingual (SLG) gland, as well as thousands of minor SGs in the oral cavity. The PG, located in front of the ear, is the largest SG in humans, but in mice and rats, the SMG is the largest. The SMG lies in the submandibular area and the SLG in the floor of the mouth (6, 24, 25). Stensen’s duct is the main excretory duct of the PG and opens into the oral cavity in the buccal mucosa near the second maxillary molar. The main excretory duct of the SMG is Wharton’s duct, which enters the oral cavity under the tongue by the lingual frenum called the sublingual caruncle. The SLG has small ducts called ducts of Rivinus and a common duct, Bartholin’s duct, which connects with Wharton’s duct at the sublingual caruncle (24, 25).
The SG is composed of parenchyma (glandular secretory tissue) with serous and mucous acinar cells, ductal cells, and myoepithelial cells along with connective tissue. Also, there are fibroblasts, immune cells, neuroendocrine cells, endothelial cells, stromal cells, and pericytes (Figure 1) (8, 13). The average daily flow of salivary secretion in adults is 1000–1500 mL/day and >90% is secreted from these three major SGs. Saliva is a fluid that contains water, ions (14, 22, 23, 26), carbohydrates, peptides (enzymes, hormones (9–12, 17–21), and immunoglobulins), exfoliated cells (epithelial and immune cells), nucleic acids, and microorganisms (Table 1). Saliva plays important roles in moistening and lubrication, mucosal protection and wound healing, anti-microbial action, tooth protection and immunization (27, 28).
Figure 1 Schematic graph of anatomy, histology, and cell types for the salivary glands and the neurocircuits of saliva secretion.
In addition, SGs are involved in neuroendocrine and endocrine functions, taste and smell perception (29, 30). The human minor SG single-cell RNA sequencing atlas (9 samples, 13,824 cells) shows not only the traditional epithelial cells such as acini cells and duct cells, but also diverse immune cells (B lymphocytes) with immunoglobins (such as IgA and IgG), neuroendocrine cells (acidic glycoprotein chromogranin A, CGA and glial cell line-derived neurotrophic factor family receptor α3), and epithelial cells with antibacterial proteins (such as lactoferrin and defensin) (31). Recently, the synthesis and production of corticosterone, testosterone, and melatonin have been reported in the SG of rats, supporting the hypothesis that the SG is an endocrine gland and is involved in the regulation of endocrine function (17, 32).
Molecular and neural mechanisms of salivary secretion
Salivation is one of the classic Pavlov’s conditioned reflexes via environment signals and neuronal mechanisms. The nervous system mediates salivary function, sensory and motor stimuli induce changes in salivary flow and components via cellular and molecular mechanisms (8, 33, 34).
Odor induces secretion from SMGs and SLGs but not PGs in humans. The salivary secretion rate increases in response to food or taste-related odors, while different taste-related odors (sweet, savory, and sour) and macronutrient-related odors (carbohydrates, proteins, fats, and low-calorie compounds) induce a similar increase in salivary secretion rate, but do not influence the viscosity, elasticity, ɑ-amylase, and lingual lipase activity. Combinations of stimuli are essential to induce higher flow rates and increase the activity of salivary enzymes to facilitate digestion (35). Human salivary proteome data show that mechanical and gustatory stimuli do not change the total protein concentration, but increases the volume and total amount of protein. It seems that masticatory and gustatory stimuli activate the parasympathetic and sympathetic nervous systems. Both chewing and gustatory stimuli co-regulate the components and concentrations of proteins in human SGs (36). Swallowing efficiency was positively correlated with cerebellar gray matter volume, however, negatively correlated with age in healthy older adults (52-82 years old, 28 female) (37). In clinical study, reconstructing physiological homeostasis of the masticatory complex decrease the thickness of the masseter muscle and increase the height of the maxillary 2nd molar with flattened occlusal curves and curves of Wilson via botulinum toxin-A injection, it seems reshaping the masticatory complex can reset the muscle-brain neurocircuits in orthodontics (38).
In humans, tastant recognition signals from the taste buds in the mouth, pharynx, and larynx are transmitted through the facial, glossopharyngeal, and vagus nerves, which terminate in the nucleus of the solitary tract in the brainstem (29, 39). A study designed multisensory food cues (1) odor, (2) odor+vision, (3) odor+vision+taste, and (4) odor+vision+taste+mastication to test the saliva secretion response. The multisensory stimuli result in significant changes in salivary secretion rate and its components depending on the combinations of sensory modalities (40). Transient receptor potential (TRP) ion channels in oral epithelial cells respond to temperature change, irritants (capsaicin), and cooling agents (menthol). Capsaicin (a TRPV1 agonist) also induces a higher sIgA secretion rate with an increase of the β-wave and heart rate variability in the electroencephalogram, TRPV1 increases the sIgA secretion rate through the sympathetic nervous system (41, 42). In another report, TRPV1 agonists (nonivamide, 6.0 × 102 ppm) and TRPM8 agonists (menthol, 1.0 × 104 ppm) also modify the components of saliva and increase protein output from whole mouth saliva. And TRPV1 agonists (nonivamide, 6.0 × 102 ppm) induce an acute salivary cystatin S response, which improves mucosal adhesion. The TRPA1 agonist cinnamaldehyde (1.8 × 104 ppm) is more effective than menthol, but it cannot evoke saliva secretion, suggesting that salivary responses are TRP agonist-specific (43).
Besides, reduced perception of basic taste and smell has been reported in older patients, while there is no significant difference in oral TRP stimulation between older and young groups, indicating that chemo-sensation is retained in the older group. Salivary viscoelasticity decreases with age (higher viscoelasticity in younger vs older groups) (44). In humans, chewing induces salivary secretion through the activation of mechanoreceptors in the periodontal ligaments, and proprioceptors and/or nociceptors in the oral mucosa (10).
The salivary flow rate follows a circadian rhythm with the acrophase at ~15:30 and falling to almost zero during sleep. The concentrations of Na+, Cl–, Ca2+, K+, and protein in whole saliva also show diverse circadian rhythms in SGs (45). There are rhythmic expression of aquaporin 5 and anoctamin 1 in rat SMG by light condition (46). Since the known clock gene, brain-muscle arnt-like 1 (Bmal1) and period 2(Per2) mRNA expression are expressed in a circadian rhythm pattern in mouse mucous acini and striated ducts, SGs might contain a peripheral clock regulating salivary flow and electrolyte flux (47).
Repeated exposure to an image consistently paired with sour candy immediately increases the saliva secretion rate, but this is not maintained in a second experiment days later (48). In general, food imagination can induce salivary secretion and the mouthwatering sensation (8). In another report, images of foods did not induce an increased salivary flow (49). Increased salivary flow has been found after seeing actual food, and much greater flow occurs when watching other people food. The belief of the participants as to whether they can actually consume these foods has an impact on saliva flow. When the same cookies are colored an unattractive green, the increased salivary flow is eliminated, confirming that humans can develop preferences for palatable food through social learning and emphasizing the importance of palatability (50). Antidepressants and antiparkinsonian medications cause xerostomia because of disturbance in the central nervous system (CNS) (51, 52), this mechanism may be the central accumulation of norepinephrine, which activates α2-adrenoceptors and decreases the activity of parasympathetic salivary neurons in the brainstem (53). Schematic graph summarized the anatomy, histology, and cell types for the salivary glands and the neurocircuits of saliva secretion (Figure 1).
The signals from taste-activated chemoreceptors, chewing-activated mechanoreceptors, or nociceptors are transmitted to the nucleus of the solitary tract and then the signals are transmitted to the salivary nuclei (54). Stimulation of the parasympathetic nerves induces protein-poor along with an increased volume of saliva via muscarinic cholinergic receptors in SG acinar cells, whereas stimulation of the sympathetic nerves induces protein-rich along with a small volume of saliva via β1-adrenoceptors (34, 55, 56). VIP mediates protein secretion and participates in parasympathetic-mediated vasodilatation. VIP-immunoreactive nerve fibers are close to acinar cells, secretory ducts, and blood vessels in human SMGs and PGs. In rat SMGs, VIP evokes acinar degranulation through cAMP-activated protein kinase A (57, 58). Polypeptides in saliva can modulate taste through interacting with the receptors on taste buds. Neuropeptide Y in saliva acts on Y2 receptors expressed in the lingual epithelial cells to induce satiation (59).
Endocrine and immune functions of salivary glands
SGs produce saliva with endocrine and immune functions, review literature overviewed the resident immune cells (B cells, T cells, macrophages, and dendritic cells) in SGs (60, 61). CgA is stored in the secretory granules of endocrine cells, and it is found in serous and ductal cells in human SMGs through immunohistochemistry (IHC) and in situ hybridization (62). In the SMGs of both rats and humans, melatonin and its synthesizing enzyme arylalkylamine N-acetyltransferase have been found in the striated ducts of SMGs; so SGs can produce melatonin (2). In human PGs, SMGs, and labial glands, melatonin is stored in the acinar cells, and released to saliva; heavy immunogold staining has been found in the PG (17). The primary substrate of steroid synthesis and enzyme activity for corticosterone and testosterone production has been detected in the rat SG (32), and estrogen receptor expression has been demonstrated in normal human minor SGs (63). Sex hormone receptors and human epidermal growth factor receptor 2 (HER-2) have been reported in both benign and malignant salivary tumors (64). Androgen receptors and HER-2 are present in high-grade SG carcinomas, and the evaluation of these hormones receptors might benefit targeted therapy or hormone treatment. Steroid hormones are thought to modulate salivary components through autocrine or paracrine pathways (32). Therefore, salivary corticosterone, testosterone, and melatonin might be derived from SGs.
SGs might be one of the critical immune organs involved in innate and adaptive immunity. Vaccines are usually delivered by intramuscular injection, and SGs can be a candidate target for enhancing the immunization response. Immunization of the SG has already been confirmed to protect lethal challenge models of infectious pathogens (65). In the lethal influenza virus infection mouse model, soluble innate inhibitors in saliva such as agglutinin can protect against lower respiratory tract infection. In mice, a potent inhibitor of the virus in saliva can stop the deposited virus in the upper respiratory tract progressing to the lower respiratory tract. Since the saliva in the oral cavity bathes the oropharynx, the potent inhibitor in the saliva can stop the virus in there (66). Since saliva exerts the action of washing away materials such as viruses, a low salivary flow may increase the risk of virus transmission, and a high flow can clean and kill the virus in short time (67, 68).
Saliva functions in innate immunity of the oral cavity may protect against demineralization of teeth. Gel-forming mucins (MUC) are a major constituent, MUC19 is the salivary MUC in mice. A study found MUC19 plays a key role in bacterial clearance, and formation of heterotypic complexes in saliva (binding Streptococcus mutans) in WT- and Mut-Muc19 mice, this represented a novel innate immune function for mucins. Human MUC19 transcripts in salivary glands (n = 7) and MUC19 glycoproteins in glandular mucous cells and saliva are also found (69). Mucosal immunity including the mucus covering the respiratory tract, surfactants, anti-infectious molecules (sIgA, defensins, and interferons), respiratory epithelial cells, and innate immunity cells (nasal goblet cells and macrophages), form a mucosal barrier that plays a vital role in COVID-19 (70). The mucosal immune system in the nasal and oral cavities, acts as the first barrier, with the appearance of sIgA in the saliva (4). It has been reported that the salivary IgA responding to SARS-CoV-2 persists long-term (3 months) and shows a weak correlation with serum IgA. This suggests that the IgA of the oral cavity comes from the SGs as sIgA (5). IgA is dominant in early virus neutralization. Furthermore, after day 49 post-symptom onset, saliva samples neutralize SARS-CoV-2-pseudotyped viral particles. Anti-receptor binding domain IgA is consistently more abundant in saliva than in serum (71). After a second mRNA vaccine injection, IgG and IgA responses to S-protein and its receptor-binding domain are detectable in human saliva (72). Furthermore, cross-reactive sIgA against SARS-CoV-2 spike 1 is detectable in saliva samples from people without SARS-CoV-2 infection (73). So specific salivary IgA, IgG, and IgM play important roles in airway defense during ongoing SARS-CoV-2 and its prognosis. The decrease in lactoferrin and IgA in COVID-19 patients suggests impairment of the immunoprotective mechanisms of the mucosal barrier; lactoferrin may play an essential role in the pathophysiology of severe cases, since these patients might be vulnerable to secondary airway infection. The concentration of lactoferrin is decreased in patients infected with COVID-19 even after rehabilitation (74). IgA can prevent mucosal infection in the mouth and airway, the lower levels of IgA damage this defense mechanism and promote infection with SARS-CoV-2 and other pathogens during and after infection.
Nasal-spray vaccines not only provoke a whole-body immune response, but also activate a mucosal immune response in the nose and respiratory tract to stop pathogens more quickly (75). Nasal vaccines can make up for the defects of mRNA vaccines in lacking respiratory mucosal immunity, in reaction to the acceleration of viruses evading the immune responses and the increase of transmissibility (76). Intranasal treatment with the novel engineered trimeric ACE2 (eT-ACE2) protein fully protected mice from a δ-variant challenge (500 pfu), and the viral load in lung homogenates was lower 4 days post-infection, while the mortality in the control group was 100% within 8 days in the absence of eT-ACE2 treatment. This study demonstrated that eT-ACE2 (1.5 mg/kg) has a high affinity for S-protein to neutralize SARS-CoV-2 (77). Reducing ACE2 protect from SARS-CoV-2 infection via a novel function of farnesoid X receptor, the drug of suppressing this receptor reduced ACE2 mRNA expression in human nasal epithelial cell (78). With regard to mesenchymal stem cell-derived extracellular vesicles from the oral cavity, a review discusses the mechanisms of how this special stem cell can improve neurodegenerative conditions (7). Enteric viruses infect SGs and release into saliva in mice (79), this indicated the viruses infection in SG and saliva as a potential risk transmission route through talking, coughing, sneezing and kissing, not just fecal contamination. The new study from healthcare workers reported the mRNA-BNT162b2 vaccination drastically induced a systemic immune response by boosting neutralizing antibodies in serum, but not in saliva, therefore oral mucosal immunity is not activated and cannot stop virus acquisition via this route (80). Mosquito (Aedes aegypti) salivary gland extract is known to regulate host immune responses and pathogen transmission, a salivary protein (LTRIN) have been identified from mosquito, this protein can facilitates the transmission of Zika virus by lymphotoxin-β receptor and interfering, LTRIN might a target for Zika infection and treatment (81). In mosquito saliva, anticoagulant, vasodilatory, and immunomodulatory activities is detectable after the bite, the review discussed the innate and adaptive response in skin to mosquito saliva (82).
Dysfunction and disorder in the salivary gland
Systemic diseases, such as infection, inflammatory disorders, genetic diseases, and neoplastic diseases and disorders impact the function of oral organs (83–85). There are many reviews of salivary function and secretion in health and disease (10, 86). Hyposalivation is the objective reduction of salivary secretion, Xerostomia is the feeling of oral dryness and a complaint in hyposalivation. Sjögren syndrome (SS) is a well-known autoimmune disease, in which the exocrine glands are primarily affected by oral dryness, and autoimmune epithelitis is its major pathogenesis. Epithelial cells act as the central regulators of autoimmune responses through presenting antigens. The accumulation of immune cells regulates the local immune responses and further activates epithelial cells leading to a vicious cycle of epithelial cell and immune cell interaction. The epithelium of the SGs is impaired by abnormal B cell and T cell infiltration and secondary chronic inflammation causes the loss of physiological functions (87). IL-17 and chemokine receptor 9+/α4β7- Th17 cells promoted the inflammation, dysfunction, and cell death in salivary gland of NOD/ShiLtJ mice, in human SS patient, serum IgA and IL-17 level are higher with lower retinoic acid level, and there are a numbers of chemokine receptor 9 and IL-17 double-positive cells in biopsy specimens of salivary gland (88). A test from the minor salivary glands of SS patients and healthy individuals, there is no significant difference in leptin expression and leptin receptor distribution in SG, therefore leptin seems not association with the pathogenesis of SS (18). In patients with plaque psoriasis, a chronic, immune-related disease, the secretory function of the PG and SMG is lost and salivary amylase activity and total protein concentration is decreased, meanwhile TNF-1, IL-2, and INF-γ level are higher with lower IL-10 (89), salivary total oxidant status and oxidative status index may be potential diagnostic biomarkers for plaque psoriasis (90).
Angiotensin-converting enzyme 2 (ACE2) and transmembrane protease serine 2 (TMPRSS2) are target molecules for SARS-CoV-2. ACE2 is the only human cellular receptor, furthermore, TMPRSS2 cleavage of the viral spike protein and ACE2 begin the host-pathogen interaction process (91, 92). In saliva, furin cleaves the S protein into S1 and S2 domains and is associated with the infectivity of SARS-CoV-2 (93). S1 with the ACE2 recognition motif is responsible for binding to the cell. The S2 domain regulates fusion of the virus with the host cell (94). So the co-expression of ACE2, TMPRSS2, and furin in the SGs is pivotal for SARS-CoV-2 to change the function of salivary secretion, IHC analyses have shown these three proteins are expressed in the SMGs of humans and rats (95). In SG sections from adult patients with benign disorders (sialolithiasis and mucocele), ACE2 and TMPRSS2 expression is present in the cytoplasm of serous acinar cells (96). Moreover, when samples of SGs from fatal COVID-19 cases are tested using qRT-PCR, IHC, electron microscopy, and histopathological analysis, infection and replication of COVID-19 are found, as shown by the presence of ACE2 and TMPRSS receptors (97). The interaction between ACE2 and the virus downregulates the receptor and induces the accumulation of angiotensin II (98), which reduces parotid secretion through vasoconstrictor action and changes in water and electrolyte transport (99). Losartan (an angiotensin II receptor blocker) decreases saliva and total protein secretion, on account of reducing the mRNA expression of the renin-angiotensin system (RAS) in the parotid and the microthrombotic occlusion in vessels of the SGs (100). The downregulation of ACE2 leads to a dysregulated RAS, inflammation, and constant damage throughout the duration of COVID-19. The plasma ACE2 activity is elevated in patients even after COVID-19 infection for 114 days (101). SARS-CoV-2 can bind to ACE2 receptors in SGs and lyses the cells to induce acute sialadenitis. Although fibrous repair and hyperplasia can repair the damage, the consequence is SG hyposecretion and stenosis in the ducts (102).
Aging is a physiological process with dry mouth and lower salivary flow rates. Fat tissue is increased in SGs from the aged population, and the proportional volume of acinar cell secretion is reduced in elderly individuals (103). Notably, the reduction in the number of olfactory and taste receptors leads to the diminished intensity of stimulation and a decrease in the blood perfusion at the glandular level in elderly individuals (103), supporting the idea that the CNS is involved in the functions of SGs.
Medication-induced salivary dysfunction is a common cause of xerostomia; the drugs target various receptors in SGs and the CNS, hyposalivation, alteration of chemical composition and physical properties, as well as cognitive functions are the causes of xerostomia (60, 104, 105). SG damage includes radiation-induced loss of acinar cells, impaired parasympathetic innervation, and damaged vascular structures (106). Atrophy of the SGs occurs secondary to their denervation in patients (107). The weight of SMGs and aquaporin 5 expression in SMGs are decreased after parasympathectomy (108). Chronic denervation of the trigeminal nerve is linked to atrophy, and increased fatty tissue in the dog PG has been reported, trigeminal dysfunction results in accumulation of abnormal saliva and decreased weight and size of the ipsilateral SG. Denervation and loss of the masticatory–salivary reflex is one of the reasons for the atrophy of SGs (109).
Endocrine diseases such as diabetes mellitus are associated with salivary gland dysfunction in humans (110), polyuria and dehydration cause reduced salivary flow. Enlarged acinar cells and ductal atrophy occur in the SMG, and salivary flow is reduced in mice with type-2 diabetes along with increased mitochondrial dysfunction and higher expression of PTEN-induced putative kinase 1 and parkin. This suggests a mitophagy mechanism in hyposalivation (111). Patients with SG dysfunction often complain about difficulty in swallowing, chewing, and speaking (51) as well as manifestations of halitosis (112), dry buccal mucosa, glossitis (113), cracked and peeling lips (114), oral candidiasis (115, 116), and active caries (117). Moreover, salivary dysfunction can have severe consequences, including appetite loss, sleep deprivation, depression, and impaired immune function. Saliva and SGs are critical for taste sensation: dissolved tastants in saliva act on the taste receptors on taste buds to produce sensation (30). Hyposalivation decreases the tastants released from foods, resulting in changed taste. Xerostomia is one of the severe consequences in patients undergoing chemotherapy (118), so it is important to assess the changes in taste and smell to guide the dosage of drug in real time, rather than computed tomography or magnetic resonance imaging. Salivary hypofunction in the elderly is associated with less food consumption. Hyposalivation impairs chewing and swallowing, resulting in the loss of appetite and an imbalance of food intake, since flavor perception contributes to food intake (119, 120). Hyposalivation in older adults along with lower nutrient intake causes further health problems (121). Besides, hyposalivation leads to insomnia, fragmented sleep, and daytime somnolence, because of drinking at night and disruption of the circadian rhythm. In SS patients, poor sleep quality results in depression and impaired immune function (122, 123). Given the deficiency of anti-viral proteins in saliva and of the oral and respiratory mucosal barrier, hyposalivation is a potential risk factor for SARAS-CoV-2 and other respiratory infections (124, 125).
Salivary biomarkers in health and diseases
Salivary biomarkers are a powerful tool for prognosis, diagnosis, and precision medicine. Increasingly, discoveries in the study of saliva and meta-analysis by clinical scientists support the conclusion that salivary biomarkers can act as a reporter for physiological and pathophysiological condition, as well as the local oral and periodontal environment. This has been applied to early detection and monitoring in health and disease (126–128).
Increases in matrix metalloproteinase (MMP)-8, MMP-9, tissue inhibitor of matrix metalloproteinase-1, myeloperoxidase, and complement component C3c in saliva are strongly correlated with periodontitis (129). The study reported increased S100A12 expression in inflamed gingival tissue and involved in periodontitis (130). And high baseline levels of complement component C3c in saliva can serve as a marker for evaluating responses to full-mouth non-surgical periodontal treatment, including oral hygiene instructions, scaling, and root planing (131).
SS is characterized by lymphoplasmacytic infiltration of the salivary and lacrimal glands. In the salivary proteome of SS patients, fatty acid-binding protein, β-actin, and glutathione S-transferase are decreased, while α-amylase precursor, cystatin precursor, and keratin6-L are increased (132). Another study reported that the levels of cystatin C, lysozyme C, and carbonic anhydrase VI are lower, while the levels of psoriasin and caspase 14 are higher in SS patients (133).
COVID-19, the infectious disease caused by SARS-CoV-2 (one of the coronaviruses), was declared a pandemic by the World Health Organization and remains at a steady state (134). Salivary testing and monitoring might provide an easy and effective point-of-care platform for the quick and long-term diagnosis of COVID-19 (135). Eleven cases out of 12 (91.67%) and 20 out of 23 (86.96%) COVID-19 patients are reported to be 2019-nCoV RNA-positive in saliva (136, 137). However, in saliva swabs, half of 15 COVID-19 patients and 13 cases out of 31 (41.94%) are 2019-nCoV RNA-positive in saliva (135, 138). The diagnostic value of saliva greatly depends on how it is obtained. In samples from salivary gland ducts, 4 of 31 COVID-19 patients (12.90%) are found to be 2019-nCoV RNA-positive (135).
Saliva is a sensitive and specific prognostic and diagnostic tool by measuring the concentration of free circulating cortisol and melatonin (139, 140). It is also used as a conventional test in clinical and basic research. Salivary samples permit the real-time diagnosis and monitoring of hormonal secretions and the control of the concentration of hormones used as drugs (such as glucocorticoid replacement therapy) (141). In 100 healthy volunteers, there are different patterns in 3 biomarkers (cortisol, amylase and CGA) on day- and night-saliva: higher level cortisol in lower BMI (body mass index) group, and higher CGA with lower amylase in older group, and lower CGA in male group (vs female); the cortisol levels follow the higher level on day with lower on night as previous studies (142). Salivary cortisol is useful for the screening of Cushing’s syndrome, it is easy to detect the impaired circadian rhythm of the hypothalamic–pituitary–adrenal axis presented by Cushing’s syndrome patients by the higher cortisol values in saliva at night (143, 144). Inflammatory profiles of saliva and serum in inflammatory bowel disease share similar elevated IL-6 and MMP-10 levels in stimulated saliva (145). Macrophage colony-stimulating factor 1 in saliva is positively associated with caries in healthy children (7–9 years old) (146).
Several cytokines in saliva have been regarded as possible biomarkers for oral squamous cell carcinoma (OSCC). Salivary IL-6 levels are elevated not only in OSCC patients but also in chronic oral inflammatory diseases such as chronic periodontitis (CP) and oral lichen planus (OLP). The salivary IL-6 level in OSCC patients is significantly higher than that of in healthy volunteers, CP, and OLP patients, indicating that IL-6 can serve as a promising biomarker for OSCC detection, and can also be biomarker for identifying CP and/or OLP (147, 148). The salivary IL-8 level is also elevated in both OSCC patients and oral pre-cancer patients compared to healthy controls, so it might be candidate for the risk of oral diseases (149).
A salivary microRNA has been reported as a new biomarker for OSCC screening. miR-30c-5p is significantly decreased in the saliva of OSCC patients. High expression of the miR-targeted genes is negatively correlated with miR-30c-5p in tissue, and this might be linked to the short overall survival in patients (150).
In HIV/SIV-induced periodontal disease in the rhesus macaques model, phytocannabinoids reduce gingival/systemic inflammation and salivary dysbiosis and improve the metabolic dysfunction (151). In children with chronic kidney disease, the higher activity of peroxidase and superoxide dismutase in stimulated saliva, as well as elevated concentrations of uric acid and albumin in non-stimulated saliva and stimulated saliva have been reported (vs control). Salivary advanced oxidation protein products can be a potential biomarker and diagnostic value in children patients. Additionally, ferric ion reducing antioxidant and uric acid in salivary are higher in children patients, it might be as marker for disease progression (152, 153). Salivary biomarkers will be effective and non-invasive in the prognosis and monitoring of disease progression and evaluating the response to treatment.
Conclusions and perspectives
In this review, we summarize the progress in studies of salivary secretion and function. Many sensory stimuli can modulate the salivary secretion, flow rate, and composition via the CNS. Substantial evidence supports the endocrine and immune functions of SGs. Abundant biomarkers in saliva are a potential tool for monitoring, prognosis, diagnosis, and precision medicine in health and disease. Based on endocrine and neuroendocrine reflexes in salivary secretion, it is necessary to explore the neural circuits in the brain–peripheral organ axis.
Author contributions
JL and XC supervised the project. YS, JL and XC wrote drafts of the manuscript. MCZ, YS, ML and TW collected the literature. All authors contributed to the article and approved the submitted version.
Funding
This work was supported by the National Natural Science Foundation of China 81970978 to JL and 81930054; 32120103007 to XQC.
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: salivary gland, endocrine gland, immune function, saliva, neuroendocrine
Citation: Shang YF, Shen YY, Zhang MC, Lv MC, Wang TY, Chen XQ and Lin J (2023) Progress in salivary glands: Endocrine glands with immune functions. Front. Endocrinol. 14:1061235. doi: 10.3389/fendo.2023.1061235
Received: 04 October 2022; Accepted: 09 January 2023;
Published: 03 February 2023.
Edited by:
Wensheng Li, Sun Yat-sen University, ChinaReviewed by:
Fengying Gong, Peking Union Medical College Hospital (CAMS), ChinaYa-Xiong Tao, Auburn University, United States
Copyright © 2023 Shang, Shen, Zhang, Lv, Wang, Chen and Lin. 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: Jun Lin, linjun2@zju.edu.cn