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Fibronectin fibril alignment is established upon initiation of extracellular matrix assembly
The physical structure of the extracellular matrix (ECM) is tissue-specific and fundamental to normal tissue function. Proper alignment of ECM fibers is essential for the functioning of a variety of tissues. While matrix assembly in general has been intensively investigated, little is known about th...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8108514/ https://www.ncbi.nlm.nih.gov/pubmed/33625865 http://dx.doi.org/10.1091/mbc.E20-08-0533 |
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author | Garrison, Carly M. Schwarzbauer, Jean E. |
author_facet | Garrison, Carly M. Schwarzbauer, Jean E. |
author_sort | Garrison, Carly M. |
collection | PubMed |
description | The physical structure of the extracellular matrix (ECM) is tissue-specific and fundamental to normal tissue function. Proper alignment of ECM fibers is essential for the functioning of a variety of tissues. While matrix assembly in general has been intensively investigated, little is known about the mechanisms required for formation of aligned ECM fibrils. We investigated the initiation of fibronectin (FN) matrix assembly using fibroblasts that assemble parallel ECM fibrils and found that matrix assembly sites, where FN fibrillogenesis is initiated, were oriented in parallel at the cell poles. We show that these polarized matrix assembly sites progress into fibrillar adhesions and ultimately into aligned FN fibrils. Cells that assemble an unaligned meshwork matrix form matrix assembly sites around the cell periphery, but the distribution of matrix assembly sites in these cells could be modulated through micropatterning or mechanical stretch. While an elongated cell shape corresponds with a polarized matrix assembly site distribution, these two features are not absolutely linked, since we discovered that transforming growth factor beta (TGF-β1) enhances matrix assembly site polarity and assembly of aligned fibrils independent of cell elongation. We conclude that the ultimate orientation of FN fibrils is determined by the alignment and distribution of matrix assembly sites that form during the initial stages of cell–FN interactions. |
format | Online Article Text |
id | pubmed-8108514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-81085142021-06-30 Fibronectin fibril alignment is established upon initiation of extracellular matrix assembly Garrison, Carly M. Schwarzbauer, Jean E. Mol Biol Cell Articles The physical structure of the extracellular matrix (ECM) is tissue-specific and fundamental to normal tissue function. Proper alignment of ECM fibers is essential for the functioning of a variety of tissues. While matrix assembly in general has been intensively investigated, little is known about the mechanisms required for formation of aligned ECM fibrils. We investigated the initiation of fibronectin (FN) matrix assembly using fibroblasts that assemble parallel ECM fibrils and found that matrix assembly sites, where FN fibrillogenesis is initiated, were oriented in parallel at the cell poles. We show that these polarized matrix assembly sites progress into fibrillar adhesions and ultimately into aligned FN fibrils. Cells that assemble an unaligned meshwork matrix form matrix assembly sites around the cell periphery, but the distribution of matrix assembly sites in these cells could be modulated through micropatterning or mechanical stretch. While an elongated cell shape corresponds with a polarized matrix assembly site distribution, these two features are not absolutely linked, since we discovered that transforming growth factor beta (TGF-β1) enhances matrix assembly site polarity and assembly of aligned fibrils independent of cell elongation. We conclude that the ultimate orientation of FN fibrils is determined by the alignment and distribution of matrix assembly sites that form during the initial stages of cell–FN interactions. The American Society for Cell Biology 2021-04-15 /pmc/articles/PMC8108514/ /pubmed/33625865 http://dx.doi.org/10.1091/mbc.E20-08-0533 Text en © 2021 Garrison and Schwarzbauer. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. https://creativecommons.org/licenses/by-nc-sa/3.0/This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License. |
spellingShingle | Articles Garrison, Carly M. Schwarzbauer, Jean E. Fibronectin fibril alignment is established upon initiation of extracellular matrix assembly |
title | Fibronectin fibril alignment is established upon initiation of extracellular matrix assembly |
title_full | Fibronectin fibril alignment is established upon initiation of extracellular matrix assembly |
title_fullStr | Fibronectin fibril alignment is established upon initiation of extracellular matrix assembly |
title_full_unstemmed | Fibronectin fibril alignment is established upon initiation of extracellular matrix assembly |
title_short | Fibronectin fibril alignment is established upon initiation of extracellular matrix assembly |
title_sort | fibronectin fibril alignment is established upon initiation of extracellular matrix assembly |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8108514/ https://www.ncbi.nlm.nih.gov/pubmed/33625865 http://dx.doi.org/10.1091/mbc.E20-08-0533 |
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