Coregulation of fibronectin signaling and matrix contraction by tenascin-C and syndecan-4.

Syndecan-4 is a ubiquitously expressed heparan sulfate proteoglycan that modulates cell interactions with the extracellular matrix. It is transiently up-regulated during tissue repair by cells that mediate wound healing. Here, we report that syndecan-4 is essential for optimal fibroblast response to...

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Main Authors: Midwood, K, Valenick, L, Hsia, H, Schwarzbauer, J
Format: Journal article
Language:English
Published: 2004
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author Midwood, K
Valenick, L
Hsia, H
Schwarzbauer, J
author_facet Midwood, K
Valenick, L
Hsia, H
Schwarzbauer, J
author_sort Midwood, K
collection OXFORD
description Syndecan-4 is a ubiquitously expressed heparan sulfate proteoglycan that modulates cell interactions with the extracellular matrix. It is transiently up-regulated during tissue repair by cells that mediate wound healing. Here, we report that syndecan-4 is essential for optimal fibroblast response to the three-dimensional fibrin-fibronectin provisional matrix that is deposited upon tissue injury. Interference with syndecan-4 function inhibits matrix contraction by preventing cell spreading, actin stress fiber formation, and activation of focal adhesion kinase and RhoA mediated-intracellular signaling pathways. Tenascin-C is an extracellular matrix protein that regulates cell response to fibronectin within the provisional matrix. Syndecan-4 is also required for tenascin-C action. Inhibition of syndecan-4 function suppresses tenascin-C activity and overexpression of syndecan-4 circumvents the effects of tenascin-C. In this way, tenascin-C and syndecan-4 work together to control fibroblast morphology and signaling and regulate events such as matrix contraction that are essential for efficient tissue repair.
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spelling oxford-uuid:994a224d-fb6a-4ae0-8016-cb550bc8f2ad2022-03-27T00:13:14ZCoregulation of fibronectin signaling and matrix contraction by tenascin-C and syndecan-4.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:994a224d-fb6a-4ae0-8016-cb550bc8f2adEnglishSymplectic Elements at Oxford2004Midwood, KValenick, LHsia, HSchwarzbauer, JSyndecan-4 is a ubiquitously expressed heparan sulfate proteoglycan that modulates cell interactions with the extracellular matrix. It is transiently up-regulated during tissue repair by cells that mediate wound healing. Here, we report that syndecan-4 is essential for optimal fibroblast response to the three-dimensional fibrin-fibronectin provisional matrix that is deposited upon tissue injury. Interference with syndecan-4 function inhibits matrix contraction by preventing cell spreading, actin stress fiber formation, and activation of focal adhesion kinase and RhoA mediated-intracellular signaling pathways. Tenascin-C is an extracellular matrix protein that regulates cell response to fibronectin within the provisional matrix. Syndecan-4 is also required for tenascin-C action. Inhibition of syndecan-4 function suppresses tenascin-C activity and overexpression of syndecan-4 circumvents the effects of tenascin-C. In this way, tenascin-C and syndecan-4 work together to control fibroblast morphology and signaling and regulate events such as matrix contraction that are essential for efficient tissue repair.
spellingShingle Midwood, K
Valenick, L
Hsia, H
Schwarzbauer, J
Coregulation of fibronectin signaling and matrix contraction by tenascin-C and syndecan-4.
title Coregulation of fibronectin signaling and matrix contraction by tenascin-C and syndecan-4.
title_full Coregulation of fibronectin signaling and matrix contraction by tenascin-C and syndecan-4.
title_fullStr Coregulation of fibronectin signaling and matrix contraction by tenascin-C and syndecan-4.
title_full_unstemmed Coregulation of fibronectin signaling and matrix contraction by tenascin-C and syndecan-4.
title_short Coregulation of fibronectin signaling and matrix contraction by tenascin-C and syndecan-4.
title_sort coregulation of fibronectin signaling and matrix contraction by tenascin c and syndecan 4
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