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Molecular Cues Guiding Matrix Stiffness in Liver Fibrosis
Tissue and matrix stiffness affect cell properties during morphogenesis, cell growth, differentiation, and migration and are altered in the tissue remodeling following injury and the pathological progression. However, detailed molecular mechanisms underlying alterations of stiffness in vivo are stil...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075297/ https://www.ncbi.nlm.nih.gov/pubmed/27800489 http://dx.doi.org/10.1155/2016/2646212 |
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author | Saneyasu, Takaoki Akhtar, Riaz Sakai, Takao |
author_facet | Saneyasu, Takaoki Akhtar, Riaz Sakai, Takao |
author_sort | Saneyasu, Takaoki |
collection | PubMed |
description | Tissue and matrix stiffness affect cell properties during morphogenesis, cell growth, differentiation, and migration and are altered in the tissue remodeling following injury and the pathological progression. However, detailed molecular mechanisms underlying alterations of stiffness in vivo are still poorly understood. Recent engineering technologies have developed powerful techniques to characterize the mechanical properties of cell and matrix at nanoscale levels. Extracellular matrix (ECM) influences mechanical tension and activation of pathogenic signaling during the development of chronic fibrotic diseases. In this short review, we will focus on the present knowledge of the mechanisms of how ECM stiffness is regulated during the development of liver fibrosis and the molecules involved in ECM stiffness as a potential therapeutic target for liver fibrosis. |
format | Online Article Text |
id | pubmed-5075297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-50752972016-10-31 Molecular Cues Guiding Matrix Stiffness in Liver Fibrosis Saneyasu, Takaoki Akhtar, Riaz Sakai, Takao Biomed Res Int Review Article Tissue and matrix stiffness affect cell properties during morphogenesis, cell growth, differentiation, and migration and are altered in the tissue remodeling following injury and the pathological progression. However, detailed molecular mechanisms underlying alterations of stiffness in vivo are still poorly understood. Recent engineering technologies have developed powerful techniques to characterize the mechanical properties of cell and matrix at nanoscale levels. Extracellular matrix (ECM) influences mechanical tension and activation of pathogenic signaling during the development of chronic fibrotic diseases. In this short review, we will focus on the present knowledge of the mechanisms of how ECM stiffness is regulated during the development of liver fibrosis and the molecules involved in ECM stiffness as a potential therapeutic target for liver fibrosis. Hindawi Publishing Corporation 2016 2016-10-09 /pmc/articles/PMC5075297/ /pubmed/27800489 http://dx.doi.org/10.1155/2016/2646212 Text en Copyright © 2016 Takaoki Saneyasu et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Saneyasu, Takaoki Akhtar, Riaz Sakai, Takao Molecular Cues Guiding Matrix Stiffness in Liver Fibrosis |
title | Molecular Cues Guiding Matrix Stiffness in Liver Fibrosis |
title_full | Molecular Cues Guiding Matrix Stiffness in Liver Fibrosis |
title_fullStr | Molecular Cues Guiding Matrix Stiffness in Liver Fibrosis |
title_full_unstemmed | Molecular Cues Guiding Matrix Stiffness in Liver Fibrosis |
title_short | Molecular Cues Guiding Matrix Stiffness in Liver Fibrosis |
title_sort | molecular cues guiding matrix stiffness in liver fibrosis |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075297/ https://www.ncbi.nlm.nih.gov/pubmed/27800489 http://dx.doi.org/10.1155/2016/2646212 |
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