<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Stewart DC</submitter><funding>NCRR NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIAMS NIH HHS</funding><funding>Russian Science Foundation</funding><funding>Perelman School of Medicine, University of Pennsylvania</funding><funding>NIH HHS</funding><funding>NIGMS NIH HHS</funding><funding>National Science Foundation</funding><pagination>919-938.e14</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12359077</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>145(4)</volume><pubmed_abstract>Postnatal cutaneous wound healing is characterized by development of a collagen-rich scar lacking the architecture and functional integrity of unwounded tissue. Directing cell behaviors to efficiently heal wounds while minimizing scar formation remains a major wound management goal. In this study, we demonstrate type III collagen (COL3) as a critical regulator of re-epithelialization and scar formation during healing of COL3-enriched, regenerative (Acomys), scar-permissive (CD-1 Mus and wild-type Col3&lt;sup>B6/B6&lt;/sup> mice) and COL3-deficient, scar-promoting (Col3&lt;sup>F/F&lt;/sup>, a murine conditional knockdown model) cutaneous wound models. We define a scar-permissive fibrillar collagen architecture signature characterized by elongated and anisotropically aligned collagen fibers that is dose</pubmed_abstract><journal>The Journal of investigative dermatology</journal><pubmed_title>Type III Collagen Regulates Matrix Architecture and Mechanosensing during Wound Healing.</pubmed_title><pmcid>PMC12359077</pmcid><funding_grant_id>S10OD021633</funding_grant_id><funding_grant_id>S10 RR027128</funding_grant_id><funding_grant_id>P30AR069589</funding_grant_id><funding_grant_id>R01 GM124091</funding_grant_id><funding_grant_id>R01GM124091</funding_grant_id><funding_grant_id>P30 AR069589</funding_grant_id><funding_grant_id>CMMI-1751898</funding_grant_id><funding_grant_id>S10 OD021633</funding_grant_id><funding_grant_id>S10RR027128</funding_grant_id><pubmed_authors>Maden M</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Ruthel G</pubmed_authors><pubmed_authors>Yen WK</pubmed_authors><pubmed_authors>Mauck RL</pubmed_authors><pubmed_authors>Han L</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Volk SW</pubmed_authors><pubmed_authors>Brisson BK</pubmed_authors><pubmed_authors>Gullberg D</pubmed_authors><pubmed_authors>Stewart DC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Type III Collagen Regulates Matrix Architecture and Mechanosensing during Wound Healing.</name><description>Postnatal cutaneous wound healing is characterized by development of a collagen-rich scar lacking the architecture and functional integrity of unwounded tissue. Directing cell behaviors to efficiently heal wounds while minimizing scar formation remains a major wound management goal. In this study, we demonstrate type III collagen (COL3) as a critical regulator of re-epithelialization and scar formation during healing of COL3-enriched, regenerative (Acomys), scar-permissive (CD-1 Mus and wild-type Col3&lt;sup>B6/B6&lt;/sup> mice) and COL3-deficient, scar-promoting (Col3&lt;sup>F/F&lt;/sup>, a murine conditional knockdown model) cutaneous wound models. We define a scar-permissive fibrillar collagen architecture signature characterized by elongated and anisotropically aligned collagen fibers that is dose</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Apr</publication><modification>2026-05-29T10:30:23.799Z</modification><creation>2026-04-08T04:30:04.246Z</creation></dates><accession>S-EPMC12359077</accession><cross_references><pubmed>39236902</pubmed><doi>10.1016/j.jid.2024.08.013</doi></cross_references></HashMap>