» Articles » PMID: 28424587

Interactions of the Mechanosensitive Channels with Extracellular Matrix, Integrins, and Cytoskeletal Network in Osmosensation

Overview
Specialty Molecular Biology
Date 2017 Apr 21
PMID 28424587
Citations 13
Authors
Affiliations
Soon will be listed here.
Abstract

Life is maintained in a sea water-like internal environment. The homeostasis of this environment is dependent on osmosensory system translation of hydromineral information into osmotic regulatory machinery at system, tissue and cell levels. In the osmosensation, hydromineral information can be converted into cellular reactions through osmoreceptors, which changes thirst and drinking, secretion of antidiuretic vasopressin (VP), reabsorption of water and salt in the kidneys at systemic level as well as cellular metabolic activity and survival status at tissue level. The key feature of osmosensation is the activation of mechanoreceptors or mechanosensors, particularly transient receptor potential vallinoid (TRPV) and canonical (TRPC) family channels, which increases cytosolic Ca levels, activates osmosensory cells including VP neurons and triggers a series of secondary reactions. TRPV channels are sensitive to both hyperosmotic and hyposmotic stimuli while TRPC channels are more sensitive to hyposmotic challenge in neurons. The activation of TRP channels relies on changes in cell volume, membrane stretch and cytoskeletal reorganization as well as hydration status of extracellular matrix (ECM) and activity of integrins. Different families of TRP channels could be activated differently in response to hyperosmotic and hyposmotic stimuli in different spatiotemporal orders, leading to differential reactions of osmosensory cells. Together, they constitute the osmosensory machinery. The activation of this osmoreceptor complex is also associated with the activity of other osmolarity-regulating organelles, such as water channel protein aquaporins, Na-K-2Cl cotransporters, volume-sensitive anion channels, sodium pump and purinergic receptors in addition to intercellular interactions, typically astrocytic neuronal interactions. In this article, we review our current understandings of the composition of osmoreceptors and the processes of osmosensation.

Citing Articles

TRPV1-dependent NKCC1 activation in mouse lens involves integrin and the tubulin cytoskeleton.

Shahidullah M, Mandal A, Delamere N J Cell Physiol. 2024; 239(11):e31369.

PMID: 39014912 PMC: 11560586. DOI: 10.1002/jcp.31369.


The Emergence of TRP Channels Interactome as a Potential Therapeutic Target in Pancreatic Ductal Adenocarcinoma.

Wei Y, Khalaf A, Rui C, Abdul Kadir S, Zainol J, Oglah Z Biomedicines. 2023; 11(4).

PMID: 37189782 PMC: 10136338. DOI: 10.3390/biomedicines11041164.


Focusing on Mechanoregulation Axis in Fibrosis: Sensing, Transduction and Effecting.

Wen D, Gao Y, Ho C, Yu L, Zhang Y, Lyu G Front Mol Biosci. 2022; 9:804680.

PMID: 35359592 PMC: 8963247. DOI: 10.3389/fmolb.2022.804680.


With an Ear Up against the Wall: An Update on Mechanoperception in .

Behnami S, Bonetta D Plants (Basel). 2021; 10(8).

PMID: 34451632 PMC: 8398075. DOI: 10.3390/plants10081587.


TRPV Protein Family-From Mechanosensing to Cancer Invasion.

Karki T, Tojkander S Biomolecules. 2021; 11(7).

PMID: 34356643 PMC: 8301805. DOI: 10.3390/biom11071019.


References
1.
Zhao X, Yan X, Liu Y, Zhang P, Ni X . Co-expression of mouse TMEM63A, TMEM63B and TMEM63C confers hyperosmolarity activated ion currents in HEK293 cells. Cell Biochem Funct. 2016; 34(4):238-41. DOI: 10.1002/cbf.3185. View

2.
Verbalis J . Brain volume regulation in response to changes in osmolality. Neuroscience. 2010; 168(4):862-70. DOI: 10.1016/j.neuroscience.2010.03.042. View

3.
Hollborn M, Vogler S, Reichenbach A, Wiedemann P, Bringmann A, Kohen L . Regulation of the hyperosmotic induction of aquaporin 5 and VEGF in retinal pigment epithelial cells: involvement of NFAT5. Mol Vis. 2015; 21:360-77. PMC: 4390809. View

4.
Yagil C, Sladek C . Osmotic regulation of vasopressin and oxytocin release is rate sensitive in hypothalamoneurohypophysial explants. Am J Physiol. 1990; 258(2 Pt 2):R492-500. DOI: 10.1152/ajpregu.1990.258.2.R492. View

5.
Aure M, Roed A, Galtung H . Intracellular Ca2+ responses and cell volume regulation upon cholinergic and purinergic stimulation in an immortalized salivary cell line. Eur J Oral Sci. 2010; 118(3):237-44. DOI: 10.1111/j.1600-0722.2010.00738.x. View