Physiological Cooperation between Aquaporin 5 and TRPV4: Comparison
View Latest Version
Please note this is a comparison between Version 2 by Jason Zhu and Version 1 by Eszter Ducza.

Aquaporins—among them, AQP5—are responsible for transporting water across biological

membranes, which is an important process in all living organisms. The transient receptor potential

channel 4 (TRPV4) is a cation channel that is mostly calcium-permeable and can also be activated by

osmotic stimuli. It plays a role in a number of different functions in the body, e.g., the development

of bones and cartilage, and it is involved in the body’s osmoregulation, the generation of certain

types of sensation (pain), and apoptosis. Our earlier studies on the uterus and the literature data

aroused our interest in the physiological role of the cooperation of AQP5 and TRPV4. In this review,

we focus on the co-expression and cooperation of AQP5 and TRPV4 in the lung, salivary glands,

uterus, adipose tissues, and lens. Understanding the cooperation between AQP5 and TRPV4 may

contribute to the development of new drug candidates and the therapy of several disorders (e.g.,

preterm birth, cataract, ischemia/reperfusion-induced edema, exercise- or cold-induced asthma).

Aquaporins—among them, AQP5—are responsible for transporting water across biological membranes, which is an important process in all living organisms. The transient receptor potential channel 4 (TRPV4) is a cation channel that is mostly calcium-permeable and can also be activated by osmotic stimuli. It plays a role in a number of different functions in the body, e.g., the development of bones and cartilage, and it is involved in the body’s osmoregulation, the generation of certain types of sensation (pain), and apoptosis. Earlier studies on the uterus and the literature data aroused the interest in the physiological role of the cooperation of AQP5 and TRPV4. Understanding the cooperation between AQP5 and TRPV4 may contribute to the development of new drug candidates and the therapy of several disorders (e.g., preterm birth, cataract, ischemia/reperfusion-induced edema, exercise- or cold-induced asthma).

  • AQP5
  • TRPV4
  • cooperation

1. Lung

AQP5 channels are present in the alveolar epithelium of the lung, in the apical membrane of alveolar type 1 cells of mice, rats, and humans. They mediate the transport of water molecules, mostly the transcellular water pathway [29,30][1].
AQP5 is expressed at sites where extracellular osmolality fluctuates and exposure of mouse lung epithelial cells to hyposmolality was found to result in a dose-dependent decrease in AQP5 expression. It was found that the TRPV4 channel may have an important role in the AQP5 expression changes under hypotonic conditions. The hypotonic reduction of AQP5 was blocked by TRPV4 antagonists (ruthenium red, methanandamide, and miconazole) in lung epithelial cells.
The relationship between AQP5 expression and calcium was also examined, and it was found that, in a normal medium or calcium-containing Krebs medium diluted to generate a hypotonic medium, AQP5 expression is reduced by hypotonic stress; in contrast, nothing happens to AQP5 in the calcium-free diluted Krebs medium. This is evidence that AQP5 needs Ca2+ for hypotonic reduction. To prove the presumption that TRPV4 and AQP5 can cooperate, HEK (human embryonic kidney) cells were examined. When AQP5 was transfected into control HEK cells in which there was no TRPV4, AQP5 reduction was not detected, but when AQP5 was transfected into HEK cells expressing TRPV4, a significant decrease in AQP5 abundance was found. This decrease was also sensitive to ruthenium red; it could be blocked by ruthenium red. These results suggest that TRPV4 is involved in the hypotonic stress-induced modulation of AQP5 abundance [31][2].
Other studies also examined the relationship between TRPV4 and AQP5 in the lung. Weber et al. investigated TRPV4-/- and WT (wild type) alveolar epithelial type I (ATI) cells. It was found that the AQP5 total expression levels and plasma membrane localization are lower in the TRPV4-/- ATI cells than in the wild-type cells. This was examined with fluorescence-coupled antibodies and then supported with Western blot studies, where they found the same: AQP5 expression was reduced in the TRPV4-/- cells compared to the WT cells [32,33][3][4].
Sidhaye et al. examined AQP5 regulation under shear stress, and they found that AQP5 abundance was decreased as a result of shear stress, but this decrease could be prevented by the TRPV antagonist (ruthenium red). The studies were performed in primary human bronchial epithelial cells (NBHE). VGCC (voltage-gated calcium channel) was also found to participate in the regulation of AQP5. TRPV4 activation by 4αPDD (4α-phorbol 12,13-didecanoate, which is a selective TRPV4 agonist [34][5]) was associated with a decrease in AQP5 abundance, but this effect can be blocked by nifedipine (an agent inhibiting VGCC). In contrast, the activation of VGCC (with BayK-8644) also has the same effect on AQP5, but ruthenium red cannot prevent the decrease in AQP5 abundance [35][6].
There is some information about COVID-19 linkage with AQP5 and TRPV4 channels. AQP5 expression is also regulated by inflammatory cytokines, and the elevated level of TNF-α decreases AQP5 expression in mice [36][7], which has a high volume in inflammatory respiratory diseases such as COVID-19 [30][1]. The decreased AQP5 expression may induce the activation of the TRPV4 channel, which causes the loss of the alveo-capillary barrier function and subsequently the development of edema [37,38][8][9].

2. Salivary Gland Cells

As in the lung, signs of TRPV4 and AQP5 channel cooperation were observed in salivary gland cells. Both channels are localized in the apical region of mouse submandibular gland acinar cells [39,40][10][11]. The examination of salivary gland cells from AQP5-/- and AQP5+/+ mice revealed that when they were placed in HTS (hypotonic external solution), the HTS-stimulated Ca2+ entry (for which the TRPV4 channel is probably responsible) was significantly decreased in cells isolated from AQP5-/- mice [22][12].
To investigate the relationship between AQP5 and TRPV4 in more detail, N and C terminus-truncated AQP5 channels were formed. The expression of N terminus-deleted AQP5 suppressed TRPV4 activation and regulatory volume decrease, but not cell swelling. C-terminal deletion of AQP5 has been shown to disrupt its trafficking to the apical membrane, resulting in the retention of the protein in the cell. Furthermore, hypotonicity increased the association and surface expression of AQP5 and TRPV4. These data demonstrate that the activation of TRPV4 by hypotonicity depends on AQP5, not on cell swelling per se, and that TRPV4 and AQP5 concertedly control regulatory volume decrease [22,39,41][10][12][13].

3. Uterus

AQP5 and TRPV4 channels are also found in uterine tissue [26][14]. In ourthe studies, weresearchers demonstrated the presence of AQP1, 2, 3, 5, 8, and 9 in the late-pregnancy rat uterus, with a prevalent accumulation of the AQP5 subtype near parturition [14][15]. It was established that the AQP5 expression level and myometrial contraction have an inverse correlation in the late-pregnant rat uterus [42][16]. AQP5 expression significantly increased during days 18–21 of pregnancy, and it dramatically decreased on the day of delivery (day 22). Additionally, it was demonstrated that oxytocin specifically downregulated this particular sort of water channel, whereas progesterone and progesterone analogs increased AQP5 expression, which was even more dominant than the estrogenic effect [14,42][15][16]. TRPV4 was reported to have potential influence on uterine smooth muscle contraction in both pregnant and non-pregnant uteri [43,44][17][18]. It was found that TRPV4 expression changes in correlation with the days of gestation, showing the lowest expression on day 18. In addition, this determined an inverse correlation in TRPV4 and AQP5 expression in the uterine tissue based on immunohistochemical studies [26][14]. TRPV4 expression changes through pregnancy and appears to be progesterone-dependent [45][19]. The progesterone analog levonorgestrel can downregulate TRPV4 expression [45][19], and the progesterone level falls at the end of pregnancy [46][20], which increases TRPV4 expression. Progesterone causes an increase in the AQP5 channel, suggesting that there be may a hormone-dependent cooperation between AQP5 and TRPV4 expression [26][14]. The TRPV4 channel can be activated by osmotic stimuli, and the channels are co-expressed in the uterus; therefore, AQP5 expression change triggering osmotic stress, which activates TRPV4, could be a possible mechanism for their relationship. Subsequently, TRPV4 activation causes Ca2+ flow, which contributes to the creation of uterine contractions [26][14].
Citral ((2E)-3,7-dimethylocta-2,6-dienal) is a bioactive component of lemongrass, a naturally occurring TRPV4 antagonist used to investigate the relationship between TRPV4 and AQP5 channels in the late-pregnant rat uterus [47][21]. It was found that AQP5 expression significantly increased, and TRPV4 expression did not change significantly after citral incubation in the 22-day pregnant rat uteri, in vitro. In addition, citral treatment significantly prolonged the normal gestation period and delayed preterm delivery.
TRPV4 and AQP5 are known to have an inverse co-expression in the late-pregnant rat uterus [26][14]. This may lead to the conclusion that from the 18th day of the gestation period, AQP5 expression increases, and a hypotonic milieu develops in the cytoplasm of the uterine cell, which causes smooth muscle cell membrane stretching, which triggers the activation and increased expression of the TRPV4 osmotically sensitive channel. The activation of TRPV4 leads to the Ca2+ current, which in turn plays a role in myometrial contractions and thus in the induction of labor. The decrease in AQP5 expression on the day of delivery can be explained as a result of cell volume regulation [47][21].

4. Adipose Tissues

It is a relatively new hypothesis that in obesity, where the hypothalamus receives and integrates signals from peripheral tissues (e.g., adipose and liver) and actively sends signals to manage energy balance, tissue-to-tissue co-expression (TTC) networks may reinforce communication between tissues and clarify genes or sets of genes active in one tissue that are able to induce gene activity changes in other tissues. The most connected hypothalamus gene in this network is Aqp5, which is linked to 169 adipose genes, while the adipose gene Aqp5 is only linked to 2 genes in the hypothalamus. AQP5 in the hypothalamus either ‘sends’ information to the 169 adipose genes (that is, regulates the expression of the 169 adipose genes) or ‘integrates’ (responds to) their signals [48][22].
Madeira et al. made observations to reveal the presence of AQP5 in both 3T3-L1 fibroblasts and mature adipocytes by gene expression analysis. Their results show that human AQP5 is a functional water channel when expressed in adipocytes, and their role may rely on the coordination with specific functional partners in adipocytes. Moreover, the adipose tissue expresses high levels of TRPV4, and the relationship between obesity and TRPV4 has been proven in mice. Mice with a null mutation for TRPV4, or wild-type mice treated with a TRPV4 antagonist, showed elevated thermogenesis in adipose tissues and were protected from diet-induced obesity, adipose inflammation, and insulin resistance [50,51][23][24].

5. Lens

AQP5 forms functional water channels in the rodent lens, and the dynamic membrane insertion of AQP5 may regulate water fluxes in the lens by modulating water permeability in the outer cortex [52][25]. A missense mutation in AQP5 (c.152 T > C, p. L51P) is associated with autosomal dominant congenital cataract, because AQP5 can participate in the maintenance of lens transparency by regulating vimentin expression via miR-124–3p.1 [53][26].
Lens water transport generates a hydrostatic pressure gradient that is regulated by a dual-feedback system through TRPV1 and TRPV4, to sense changes in mechanical tension and extracellular osmolarity. In this system, TRPV1 and TRPV4 reciprocally transduce changes in lens pressure into the modulation of ion transporter activity to effect alterations in circulating ion and water fluxes that act to restore the pressure gradient.
The transport of water through the mouse lens driven by the microcirculation system can be dynamically regulated by stimuli external to the lens, too. Pilocarpine (a muscarinic agonist) treatment induces the removal of TRPV4 from the membrane, increases the hydrostatic pressure gradient, and removes AQP5 from the membranes of peripheral fiber cells located in the anterior influx pathway and equatorial efflux zone. In this situation, TRPV1/4 activation has been linked to AQP5 membrane trafficking, which increases water permeability, and the changes in zonular tension would induce localized changes in water permeability that alter the relative contributions of water influx via the anterior and posterior poles, which would in turn change the curvature of the anterior surface of the aspheric mouse lens [54,55][27][28].

6. Skin

Alterations in AQP levels have been observed in skin diseases with a defective skin barrier such as hidradenitis suppurativa, atopic dermatitis, and psoriasis. AQP5 is mainly distributed in the sweat gland secretory cells and sweat gland excretory duct cells. Downregulation of AQP5 expression was determined in hidradenitis suppurativa and atopic dermatitis [56][29].
AQP5 can regulate keratinocyte proliferation and differentiation, too. AQP5 overexpression in human epidermal keratinocytes (HaCaT) could induce proliferation and dedifferentiation but not influence the apoptosis of HaCaT cells, suggesting that AQP5 mediated the balance between epidermal keratinocyte proliferation and differentiation and may play an important role in maintaining the potential of keratinocytes [57][30]. Keratinocytes also express some members of the vanilloid subfamily of TRP channels, e.g., TRPV1, TRPV3, and TRPV4.
TRPV4 is activated by changes in osmolarity, and it has been suggested that TRPV4 might act as a sensor of humidity or water flux from the skin surface as part of the epidermal permeability barrier homeostasis, as wresearchers have written before. TRPV4 belongs to a group of temperature-sensitive TRP channels, and it is activated by temperatures in the physiological skin temperature range. Warmth activation of TRPV4 leads to a Ca2+ influx through the channels, and the increase in intracellular Ca2+ concentration promotes Rho activation, which leads to the reorganization of the actin cytoskeleton and enhanced integrity of the intercellular junctions and, hence, enhanced barrier function. Therefore, it appears that keratinocytes might have a central role in the thermosensation of the skin that is mediated, at least in part, by TRPV4 channels [58][31].
AQP5 and TRPV4 proteins are both expressed in the upper layers of the palm epidermis. In an in vitro patch clamp assay, the basal activity of TRPV4 was increased in the presence of mutant AQP5 compared with the activity seen with wild-type AQP5. Therefore, AQP5 and TRPV4 might have a similar interaction in keratinocytes for detecting and responding to osmotic and mechanical stress by modulating the epidermal barrier, in particular through alterations in cell–cell junctions, such as the tight junctions [59][32].

References

  1. Cui, X.; Chen, W.; Zhou, H.; Gong, Y.; Zhu, B.; Lv, X.; Guo, H.; Duan, J.; Zhou, J.; Marcon, E.; et al. Pulmonary Edema in COVID-19 Patients: Mechanisms and Treatment Potential. Front. Pharmacol. 2021, 12, 664349.
  2. Sidhaye, V.K.; Güler, A.D.; Schweitzer, K.S.; D’Alessio, F.; Caterina, M.J.; King, L.S. Transient receptor potential vanilloid 4 regulates aquaporin-5 abundance under hypotonic conditions. Proc. Natl. Acad. Sci. USA 2006, 103, 4747–4752.
  3. Weber, J.; Rajan, S.; Schremmer, C.; Chao, Y.-K.; Krasteva-Christ, G.; Kannler, M.; Yildirim, A.Ö.; Brosien, M.; Schredelseker, J.; Weissmann, N.; et al. TRPV4 channels are essential for alveolar epithelial barrier function as protection from lung edema. JCI Insight 2020, 5, e134464.
  4. Rajan, S.; Schremmer, C.; Weber, J.; Alt, P.; Geiger, F.; Dietrich, A. Ca2+ Signaling by TRPV4 Channels in Respiratory Function and Disease. Cells 2021, 10, 822.
  5. Watanabe, H.; Davis, J.B.; Smart, D.; Jerman, J.C.; Smith, G.D.; Hayes, P.; Vriens, J.; Cairns, W.; Wissenbach, U.; Prenen, J.; et al. Activation of TRPV4 channels (hVRL-2/mTRP12) by phorbol derivatives. J. Biol. Chem. 2002, 277, 13569–13577.
  6. Sidhaye, V.K.; Schweitzer, K.S.; Caterina, M.J.; Shimoda, L.; King, L.S. Shear stress regulates aquaporin-5 and airway epithelial barrier function. Proc. Natl. Acad. Sci. USA 2008, 105, 3345–3350.
  7. Towne, J.E.; Krane, C.M.; Bachurski, C.J.; Menon, A.G. Tumor Necrosis Factor-α Inhibits Aquaporin 5 Expression in Mouse Lung Epithelial Cells. J. Biol. Chem. 2001, 276, 18657–18664.
  8. Alvarez, D.F.; King, J.A.; Weber, D.; Addison, E.; Liedtke, W.; Townsley, M.I. Transient receptor potential vanilloid 4-mediated disruption of the alveolar septal barrier: A novel mechanism of acute lung injury. Circ. Res. 2006, 99, 988–995.
  9. Hui, D.S.C.; Zumla, A. Severe Acute Respiratory Syndrome: Historical, Epidemiologic, and Clinical Features. Infect. Dis. Clin. N. Am. 2019, 33, 869–889.
  10. Liu, X.; Bandyopadhyay, B.C.; Nakamoto, T.; Singh, B.B.; Liedtke, W.; Melvin, J.E.; Ambudkar, I.S. A role for AQP5 in activation of TRPV4 by hypotonicity: Concerted involvement of AQP5 and TRPV4 in regulation of cell volume recovery. J. Biol. Chem. 2006, 283, 3688.
  11. He, X.; Tse, C.-M.; Donowitz, M.; Alper, S.L.; Gabriel, S.E.; Baum, B.J. Polarized distribution of key membrane transport proteins in the rat submandibular gland. Pflug. Arch. 1997, 433, 260–268.
  12. Arniges, M.; Vázquez, E.; Fernández-Fernández, J.M.; Valverde, M.A. Swelling-activated Ca2+ Entry via TRPV4 Channel Is Defective in Cystic Fibrosis Airway Epithelia. J. Biol. Chem. 2004, 279, 54062–54068.
  13. Hosoi, K. Physiological role of aquaporin 5 in salivary glands. Pflug. Arch. 2016, 468, 519–539.
  14. Ducza, E.; Csányi, A.; Szőke, É.; Pohóczky, K.; Hajagos-Tóth, J.; Kothencz, A.; Tiszai, Z.; Gáspár, R. Significance of transient receptor potential vanilloid 4 and aquaporin 5 co-expression in the rat uterus at term. Heliyon 2019, 5, e02697.
  15. Ducza, E.; Seres, A.B.; Hajagos-Tóth, J.; Falkay, G.; Gáspár, R. Oxytocin regulates the expression of aquaporin 5 in the late-pregnant rat uterus. Mol. Reprod. Dev. 2014, 81, 524–530.
  16. Csányi, A.; Bóta, J.; Falkay, G.; Gáspár, R.; Ducza, E. The Effects of Female Sexual Hormones on the Expression of Aquaporin 5 in the Late-Pregnant Rat Uterus. Int. J. Mol. Sci. 2016, 17, 1300.
  17. Singh, V.; Ram, M.; Kandasamy, K.; Thangamalai, R.; Choudhary, S.; Dash, J.R.; Kumar, D.; Parida, S.; Singh, T.U.; Mishra, S.K. Molecular and functional characterization of TRPV4 channels in pregnant and nonpregnant mouse uterus. Life Sci. 2015, 122, 51–58.
  18. Ying, L.; Becard, M.; Lyell, D.; Han, X.; Shortliffe, L.; Husted, C.I.; Alvira, C.M.; Cornfield, D.N. The transient receptor potential vanilloid 4 channel modulates uterine tone during pregnancy. Sci. Transl. Med. 2015, 7, 319ra204.
  19. Li, C.; Wu, Y.; Zhu, Q.; Zhang, H.-Y.; Huang, Z.; Zhang, D.; Qi, H.; Liang, G.-L.; He, X.-Q.; Wang, X.-F.; et al. TRPV4 is involved in levonorgestrel-induced reduction in oviduct ciliary beating. J. Pathol. 2019, 248, 77–87.
  20. Boroditsky, R.S.; Reyes, F.I.; Winter, J.S.; Faiman, C. Maternal serum estrogen and progesterone concentrations preceding normal labor. Obstet. Gynecol. 1978, 51, 686–691.
  21. Seres-Bokor, A.; Kemény, K.K.; Taherigorji, H.; Schaffer, A.; Kothencz, A.; Gáspár, R.; Ducza, E. The Effect of Citral on Aquaporin 5 and Trpv4 Expressions and Uterine Contraction in Rat—An Alternative Mechanism. Life 2021, 11, 897.
  22. Dobrin, R.; Zhu, J.; Molony, C.; Argman, C.; Parrish, M.L.; Carlson, S.; Allan, M.F.; Pomp, D.; Schadt, E.E. Multi-tissue coexpression networks reveal unexpected subnetworks associated with disease. Genome Biol. 2009, 10, R55.
  23. Madeira, A.; Mósca, A.F.; Moura, T.F.; Soveral, G. Aquaporin-5 is expressed in adipocytes with implications in adipose differentiation. IUBMB Life 2015, 67, 54–60.
  24. Ye, L.; Kleiner, S.; Wu, J.; Sah, R.; Gupta, R.K.; Banks, A.S.; Cohen, P.; Khandekar, M.J.; Boström, P.; Mepani, R.J.; et al. TRPV4 Is a Regulator of Adipose Oxidative Metabolism, Inflammation, and Energy Homeostasis. Cell 2012, 151, 96–110.
  25. Petrova, R.S.; Webb, K.F.; Vaghefi, E.; Walker, K.; Schey, K.L.; Donaldson, P.J. Dynamic functional contribution of the water channel AQP5 to the water permeability of peripheral lens fiber cells. Am. J. Physiol. Physiol. 2018, 314, C191–C201.
  26. Tang, S.; Di, G.; Hu, S.; Liu, Y.; Dai, Y.; Chen, P. AQP5 regulates vimentin expression via miR-124-3p.1 to protect lens transparency. Exp. Eye Res. 2021, 205, 108485.
  27. Nakazawa, Y.; Petrova, R.S.; Sugiyama, Y.; Nagai, N.; Tamura, H.; Donaldson, P.J. Regulation of the Membrane Trafficking of the Mechanosensitive Ion Channels TRPV1 and TRPV4 by Zonular Tension, Osmotic Stress and Activators in the Mouse Lens. Int. J. Mol. Sci. 2021, 22, 12658.
  28. Petrova, R.S.; Bavana, N.; Zhao, R.; Schey, K.L.; Donaldson, P.J. Changes to Zonular Tension Alters the Subcellular Distribution of AQP5 in Regions of Influx and Efflux of Water in the Rat Lens. Investig. Opthalmology Vis. Sci. 2020, 61, 36.
  29. Tricarico, P.M.; Mentino, D.; De Marco, A.; Del Vecchio, C.; Garra, S.; Cazzato, G.; Foti, C.; Crovella, S.; Calamita, G. Aquaporins Are One of the Critical Factors in the Disruption of the Skin Barrier in Inflammatory Skin Diseases. Int. J. Mol. Sci. 2022, 23, 4020.
  30. Zhou, J.; Dong, Y.; Liu, J.; Ren, J.; Wu, J.; Zhu, N. AQP5 regulates the proliferation and differentiation of epidermal stem cells in skin aging. Braz. J. Med Biol. Res. 2020, 53, e10009.
  31. Sokabe, T.; Tominaga, M. The TRPV4 cation channel: A molecule linking skin temperature and barrier function. Commun. Integr. Biol. 2010, 3, 619–621.
  32. Diana CBlaydon David, P. Kelsell Defective channels lead to an impaired skin barrier. J. Cell Sci. 2014, 127, 4343–4350.
More
© Text is available under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/)
ScholarVision Creations
Feedback