Preventing Engrailed-1 activation in fibroblasts yields wound regeneration without scarring
Author(s) -
Shamik Mascharak,
Heather E. desJardins-Park,
Michael F. Davitt,
Michelle Griffin,
Mimi R. Borrelli,
Alessandra L. Moore,
Kellen Chen,
Bryan Duoto,
Malini Chinta,
Deshka S. Foster,
Abra H. Shen,
Michael Januszyk,
Sun Hyung Kwon,
Gerlinde Wernig,
Derrick C. Wan,
H. Peter Lorenz,
Geoffrey C. Gurtner,
Michael T. Longaker
Publication year - 2021
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.aba2374
Subject(s) - wound healing , microbiology and biotechnology , regeneration (biology) , mechanotransduction , engrailed , fibroblast , knockout mouse , biology , pathology , anatomy , immunology , medicine , in vitro , receptor , gene expression , gene , genetics , homeobox
Regeneration without scarring Wounds in adult mammals typically heal by forming fibrotic scars. Mascharaket al. found that a specific population of skin fibroblasts (Engrailed-1 lineage–negative fibroblasts) activate expression ofEngrailed-1 and turn on profibrotic cellular programs in response to local tissue mechanics in wounds (see the Perspective by Konieczny and Naik). When mechanical signaling was inhibited in these cells (using either genetic deletion or small-molecule inhibition), skin wounds in mice no longer formed scars but instead healed by regeneration, restoring skin with normal hair follicles and glands, extracellular matrix, and mechanical strength.Science , this issue p.eaba2374 ; see also p.346
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom