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CLASP1 regulates endothelial cell branching morphology and directed migration
Endothelial cell (EC) branching is critically dependent upon the dynamic nature of the microtubule (MT) cytoskeleton. Extracellular matrix (ECM) mechanosensing is a prominent mechanism by which cytoskeletal reorganization is achieved; yet how ECM-induced signaling is able to target cytoskeletal reor...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5665473/ https://www.ncbi.nlm.nih.gov/pubmed/28860131 http://dx.doi.org/10.1242/bio.028571 |
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author | Myer, Nicole M. Myers, Kenneth A. |
author_facet | Myer, Nicole M. Myers, Kenneth A. |
author_sort | Myer, Nicole M. |
collection | PubMed |
description | Endothelial cell (EC) branching is critically dependent upon the dynamic nature of the microtubule (MT) cytoskeleton. Extracellular matrix (ECM) mechanosensing is a prominent mechanism by which cytoskeletal reorganization is achieved; yet how ECM-induced signaling is able to target cytoskeletal reorganization intracellularly to facilitate productive EC branching morphogenesis is not known. Here, we tested the hypothesis that the composition and density of the ECM drive the regulation of MT growth dynamics in ECs by targeting the MT stabilizing protein, cytoplasmic linker associated protein 1 (CLASP1). High-resolution fluorescent microscopy coupled with computational image analysis reveal that CLASP1 promotes slow MT growth on glass ECMs and promotes short-lived MT growth on high-density collagen-I and fibronectin ECMs. Within EC branches, engagement of either high-density collagen-I or high-density fibronectin ECMs results in reduced MT growth speeds, while CLASP1-dependent effects on MT dynamics promotes elevated numbers of short, branched protrusions that guide persistent and directed EC migration. |
format | Online Article Text |
id | pubmed-5665473 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-56654732017-11-07 CLASP1 regulates endothelial cell branching morphology and directed migration Myer, Nicole M. Myers, Kenneth A. Biol Open Research Article Endothelial cell (EC) branching is critically dependent upon the dynamic nature of the microtubule (MT) cytoskeleton. Extracellular matrix (ECM) mechanosensing is a prominent mechanism by which cytoskeletal reorganization is achieved; yet how ECM-induced signaling is able to target cytoskeletal reorganization intracellularly to facilitate productive EC branching morphogenesis is not known. Here, we tested the hypothesis that the composition and density of the ECM drive the regulation of MT growth dynamics in ECs by targeting the MT stabilizing protein, cytoplasmic linker associated protein 1 (CLASP1). High-resolution fluorescent microscopy coupled with computational image analysis reveal that CLASP1 promotes slow MT growth on glass ECMs and promotes short-lived MT growth on high-density collagen-I and fibronectin ECMs. Within EC branches, engagement of either high-density collagen-I or high-density fibronectin ECMs results in reduced MT growth speeds, while CLASP1-dependent effects on MT dynamics promotes elevated numbers of short, branched protrusions that guide persistent and directed EC migration. The Company of Biologists Ltd 2017-08-31 /pmc/articles/PMC5665473/ /pubmed/28860131 http://dx.doi.org/10.1242/bio.028571 Text en © 2017. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Myer, Nicole M. Myers, Kenneth A. CLASP1 regulates endothelial cell branching morphology and directed migration |
title | CLASP1 regulates endothelial cell branching morphology and directed migration |
title_full | CLASP1 regulates endothelial cell branching morphology and directed migration |
title_fullStr | CLASP1 regulates endothelial cell branching morphology and directed migration |
title_full_unstemmed | CLASP1 regulates endothelial cell branching morphology and directed migration |
title_short | CLASP1 regulates endothelial cell branching morphology and directed migration |
title_sort | clasp1 regulates endothelial cell branching morphology and directed migration |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5665473/ https://www.ncbi.nlm.nih.gov/pubmed/28860131 http://dx.doi.org/10.1242/bio.028571 |
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