Cellular mechanotransduction: putting all the pieces together again
- PMID: 16675838
- DOI: 10.1096/fj.05-5424rev
Cellular mechanotransduction: putting all the pieces together again
Abstract
Analysis of cellular mechanotransduction, the mechanism by which cells convert mechanical signals into biochemical responses, has focused on identification of critical mechanosensitive molecules and cellular components. Stretch-activated ion channels, caveolae, integrins, cadherins, growth factor receptors, myosin motors, cytoskeletal filaments, nuclei, extracellular matrix, and numerous other structures and signaling molecules have all been shown to contribute to the mechanotransduction response. However, little is known about how these different molecules function within the structural context of living cells, tissues, and organs to produce the orchestrated cellular behaviors required for mechanosensation, embryogenesis, and physiological control. Recent work from a wide range of fields reveals that organ, tissue, and cell anatomy are as important for mechanotransduction as individual mechanosensitive proteins and that our bodies use structural hierarchies (systems within systems) composed of interconnected networks that span from the macroscale to the nanoscale in order to focus stresses on specific mechanotransducer molecules. The presence of isometric tension (prestress) at all levels of these multiscale networks ensures that various molecular scale mechanochemical transduction mechanisms proceed simultaneously and produce a concerted response. Future research in this area will therefore require analysis, understanding, and modeling of tensionally integrated (tensegrity) systems of mechanochemical control.
Similar articles
-
Tensegrity-based mechanosensing from macro to micro.Prog Biophys Mol Biol. 2008 Jun-Jul;97(2-3):163-79. doi: 10.1016/j.pbiomolbio.2008.02.005. Epub 2008 Feb 13. Prog Biophys Mol Biol. 2008. PMID: 18406455 Free PMC article. Review.
-
Integrins, tensegrity, and mechanotransduction.Gravit Space Biol Bull. 1997 Jun;10(2):49-55. Gravit Space Biol Bull. 1997. PMID: 11540119 Review.
-
Tensegrity: the architectural basis of cellular mechanotransduction.Annu Rev Physiol. 1997;59:575-99. doi: 10.1146/annurev.physiol.59.1.575. Annu Rev Physiol. 1997. PMID: 9074778 Review.
-
Intercellular mechanotransduction: cellular circuits that coordinate tissue responses to mechanical loading.Biochem Biophys Res Commun. 2001 Aug 3;285(5):1077-83. doi: 10.1006/bbrc.2001.5177. Biochem Biophys Res Commun. 2001. PMID: 11478763 Review.
-
Mechanosensitive channels: multiplicity of families and gating paradigms.Sci STKE. 2004 Feb 3;2004(219):re4. doi: 10.1126/stke.2192004re4. Sci STKE. 2004. PMID: 14872099 Review.
Cited by
-
Cytoskeletal prestress regulates nuclear shape and stiffness in cardiac myocytes.Exp Biol Med (Maywood). 2015 Nov;240(11):1543-54. doi: 10.1177/1535370215583799. Epub 2015 Apr 23. Exp Biol Med (Maywood). 2015. PMID: 25908635 Free PMC article.
-
Tissue engineered endometrial barrier exposed to peristaltic flow shear stresses.APL Bioeng. 2020 Jun 2;4(2):026107. doi: 10.1063/5.0001994. eCollection 2020 Jun. APL Bioeng. 2020. PMID: 32548541 Free PMC article.
-
Enhancing structural support of the dermal microenvironment activates fibroblasts, endothelial cells, and keratinocytes in aged human skin in vivo.J Invest Dermatol. 2013 Mar;133(3):658-667. doi: 10.1038/jid.2012.364. Epub 2012 Oct 25. J Invest Dermatol. 2013. PMID: 23096713 Free PMC article.
-
Biomechanical Screening of Cell Therapies for Vocal Fold Scar.Tissue Eng Part A. 2015 Sep;21(17-18):2437-47. doi: 10.1089/ten.TEA.2015.0168. Epub 2015 Jul 22. Tissue Eng Part A. 2015. PMID: 26119510 Free PMC article.
-
Mechanoregulation of YAP and TAZ in Cellular Homeostasis and Disease Progression.Front Cell Dev Biol. 2021 May 24;9:673599. doi: 10.3389/fcell.2021.673599. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 34109179 Free PMC article. Review.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources