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Cellular Mechanotransduction: From Tension to Function
Living cells are constantly exposed to mechanical stimuli arising from the surrounding extracellular matrix (ECM) or from neighboring cells. The intracellular molecular processes through which such physical cues are transformed into a biological response are collectively dubbed as mechanotransductio...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6041413/ https://www.ncbi.nlm.nih.gov/pubmed/30026699 http://dx.doi.org/10.3389/fphys.2018.00824 |
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author | Martino, Fabiana Perestrelo, Ana R. Vinarský, Vladimír Pagliari, Stefania Forte, Giancarlo |
author_facet | Martino, Fabiana Perestrelo, Ana R. Vinarský, Vladimír Pagliari, Stefania Forte, Giancarlo |
author_sort | Martino, Fabiana |
collection | PubMed |
description | Living cells are constantly exposed to mechanical stimuli arising from the surrounding extracellular matrix (ECM) or from neighboring cells. The intracellular molecular processes through which such physical cues are transformed into a biological response are collectively dubbed as mechanotransduction and are of fundamental importance to help the cell timely adapt to the continuous dynamic modifications of the microenvironment. Local changes in ECM composition and mechanics are driven by a feed forward interplay between the cell and the matrix itself, with the first depositing ECM proteins that in turn will impact on the surrounding cells. As such, these changes occur regularly during tissue development and are a hallmark of the pathologies of aging. Only lately, though, the importance of mechanical cues in controlling cell function (e.g., proliferation, differentiation, migration) has been acknowledged. Here we provide a critical review of the recent insights into the molecular basis of cellular mechanotransduction, by analyzing how mechanical stimuli get transformed into a given biological response through the activation of a peculiar genetic program. Specifically, by recapitulating the processes involved in the interpretation of ECM remodeling by Focal Adhesions at cell-matrix interphase, we revise the role of cytoskeleton tension as the second messenger of the mechanotransduction process and the action of mechano-responsive shuttling proteins converging on stage and cell-specific transcription factors. Finally, we give few paradigmatic examples highlighting the emerging role of malfunctions in cell mechanosensing apparatus in the onset and progression of pathologies. |
format | Online Article Text |
id | pubmed-6041413 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60414132018-07-19 Cellular Mechanotransduction: From Tension to Function Martino, Fabiana Perestrelo, Ana R. Vinarský, Vladimír Pagliari, Stefania Forte, Giancarlo Front Physiol Physiology Living cells are constantly exposed to mechanical stimuli arising from the surrounding extracellular matrix (ECM) or from neighboring cells. The intracellular molecular processes through which such physical cues are transformed into a biological response are collectively dubbed as mechanotransduction and are of fundamental importance to help the cell timely adapt to the continuous dynamic modifications of the microenvironment. Local changes in ECM composition and mechanics are driven by a feed forward interplay between the cell and the matrix itself, with the first depositing ECM proteins that in turn will impact on the surrounding cells. As such, these changes occur regularly during tissue development and are a hallmark of the pathologies of aging. Only lately, though, the importance of mechanical cues in controlling cell function (e.g., proliferation, differentiation, migration) has been acknowledged. Here we provide a critical review of the recent insights into the molecular basis of cellular mechanotransduction, by analyzing how mechanical stimuli get transformed into a given biological response through the activation of a peculiar genetic program. Specifically, by recapitulating the processes involved in the interpretation of ECM remodeling by Focal Adhesions at cell-matrix interphase, we revise the role of cytoskeleton tension as the second messenger of the mechanotransduction process and the action of mechano-responsive shuttling proteins converging on stage and cell-specific transcription factors. Finally, we give few paradigmatic examples highlighting the emerging role of malfunctions in cell mechanosensing apparatus in the onset and progression of pathologies. Frontiers Media S.A. 2018-07-05 /pmc/articles/PMC6041413/ /pubmed/30026699 http://dx.doi.org/10.3389/fphys.2018.00824 Text en Copyright © 2018 Martino, Perestrelo, Vinarský, Pagliari and Forte. http://creativecommons.org/licenses/by/4.0/ 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. |
spellingShingle | Physiology Martino, Fabiana Perestrelo, Ana R. Vinarský, Vladimír Pagliari, Stefania Forte, Giancarlo Cellular Mechanotransduction: From Tension to Function |
title | Cellular Mechanotransduction: From Tension to Function |
title_full | Cellular Mechanotransduction: From Tension to Function |
title_fullStr | Cellular Mechanotransduction: From Tension to Function |
title_full_unstemmed | Cellular Mechanotransduction: From Tension to Function |
title_short | Cellular Mechanotransduction: From Tension to Function |
title_sort | cellular mechanotransduction: from tension to function |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6041413/ https://www.ncbi.nlm.nih.gov/pubmed/30026699 http://dx.doi.org/10.3389/fphys.2018.00824 |
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