TY - JOUR
T1 - CD201+ fascia progenitors choreograph injury repair
AU - Correa-Gallegos, Donovan
AU - Ye, Haifeng
AU - Dasgupta, Bikram
AU - Sardogan, Aydan
AU - Kadri, Safwen
AU - Kandi, Ravinder
AU - Dai, Ruoxuan
AU - Lin, Yue
AU - Kopplin, Robert
AU - Shenai, Disha Shantaram
AU - Wannemacher, Juliane
AU - Ichijo, Ryo
AU - Jiang, Dongsheng
AU - Strunz, Maximilian
AU - Ansari, Meshal
AU - Angelidis, Illias
AU - Schiller, Herbert B.
AU - Voltz, Thomas
AU - Machens, Hans Günther
AU - Rinkevich, Yuval
N1 - Publisher Copyright:
© 2023, The Author(s).
PY - 2023/11/23
Y1 - 2023/11/23
N2 - Optimal tissue recovery and organismal survival are achieved by spatiotemporal tuning of tissue inflammation, contraction and scar formation1. Here we identify a multipotent fibroblast progenitor marked by CD201 expression in the fascia, the deepest connective tissue layer of the skin. Using skin injury models in mice, single-cell transcriptomics and genetic lineage tracing, ablation and gene deletion models, we demonstrate that CD201+ progenitors control the pace of wound healing by generating multiple specialized cell types, from proinflammatory fibroblasts to myofibroblasts, in a spatiotemporally tuned sequence. We identified retinoic acid and hypoxia signalling as the entry checkpoints into proinflammatory and myofibroblast states. Modulating CD201+ progenitor differentiation impaired the spatiotemporal appearances of fibroblasts and chronically delayed wound healing. The discovery of proinflammatory and myofibroblast progenitors and their differentiation pathways provide a new roadmap to understand and clinically treat impaired wound healing.
AB - Optimal tissue recovery and organismal survival are achieved by spatiotemporal tuning of tissue inflammation, contraction and scar formation1. Here we identify a multipotent fibroblast progenitor marked by CD201 expression in the fascia, the deepest connective tissue layer of the skin. Using skin injury models in mice, single-cell transcriptomics and genetic lineage tracing, ablation and gene deletion models, we demonstrate that CD201+ progenitors control the pace of wound healing by generating multiple specialized cell types, from proinflammatory fibroblasts to myofibroblasts, in a spatiotemporally tuned sequence. We identified retinoic acid and hypoxia signalling as the entry checkpoints into proinflammatory and myofibroblast states. Modulating CD201+ progenitor differentiation impaired the spatiotemporal appearances of fibroblasts and chronically delayed wound healing. The discovery of proinflammatory and myofibroblast progenitors and their differentiation pathways provide a new roadmap to understand and clinically treat impaired wound healing.
UR - http://www.scopus.com/inward/record.url?scp=85176382144&partnerID=8YFLogxK
U2 - 10.1038/s41586-023-06725-x
DO - 10.1038/s41586-023-06725-x
M3 - Article
AN - SCOPUS:85176382144
SN - 0028-0836
VL - 623
SP - 792
EP - 802
JO - Nature
JF - Nature
IS - 7988
ER -