TY - JOUR
T1 - Wound infiltrating adipocytes are not myofibroblasts
AU - Kalgudde Gopal, Shruthi
AU - Dai, Ruoxuan
AU - Stefanska, Ania Maria
AU - Ansari, Meshal
AU - Zhao, Jiakuan
AU - Ramesh, Pushkar
AU - Bagnoli, Johannes W.
AU - Correa-Gallegos, Donovan
AU - Lin, Yue
AU - Christ, Simon
AU - Angelidis, Ilias
AU - Lupperger, Valerio
AU - Marr, Carsten
AU - Davies, Lindsay C.
AU - Enard, Wolfgang
AU - Machens, Hans Günther
AU - Schiller, Herbert B.
AU - Jiang, Dongsheng
AU - Rinkevich, Yuval
N1 - Publisher Copyright:
© 2023, The Author(s).
PY - 2023/12
Y1 - 2023/12
N2 - The origins of wound myofibroblasts and scar tissue remains unclear, but it is assumed to involve conversion of adipocytes into myofibroblasts. Here, we directly explore the potential plasticity of adipocytes and fibroblasts after skin injury. Using genetic lineage tracing and live imaging in explants and in wounded animals, we observe that injury induces a transient migratory state in adipocytes with vastly distinct cell migration patterns and behaviours from fibroblasts. Furthermore, migratory adipocytes, do not contribute to scar formation and remain non-fibrogenic in vitro, in vivo and upon transplantation into wounds in animals. Using single-cell and bulk transcriptomics we confirm that wound adipocytes do not convert into fibrogenic myofibroblasts. In summary, the injury-induced migratory adipocytes remain lineage-restricted and do not converge or reprogram into a fibrosing phenotype. These findings broadly impact basic and translational strategies in the regenerative medicine field, including clinical interventions for wound repair, diabetes, and fibrotic pathologies.
AB - The origins of wound myofibroblasts and scar tissue remains unclear, but it is assumed to involve conversion of adipocytes into myofibroblasts. Here, we directly explore the potential plasticity of adipocytes and fibroblasts after skin injury. Using genetic lineage tracing and live imaging in explants and in wounded animals, we observe that injury induces a transient migratory state in adipocytes with vastly distinct cell migration patterns and behaviours from fibroblasts. Furthermore, migratory adipocytes, do not contribute to scar formation and remain non-fibrogenic in vitro, in vivo and upon transplantation into wounds in animals. Using single-cell and bulk transcriptomics we confirm that wound adipocytes do not convert into fibrogenic myofibroblasts. In summary, the injury-induced migratory adipocytes remain lineage-restricted and do not converge or reprogram into a fibrosing phenotype. These findings broadly impact basic and translational strategies in the regenerative medicine field, including clinical interventions for wound repair, diabetes, and fibrotic pathologies.
UR - http://www.scopus.com/inward/record.url?scp=85160228373&partnerID=8YFLogxK
U2 - 10.1038/s41467-023-38591-6
DO - 10.1038/s41467-023-38591-6
M3 - Article
C2 - 37230982
AN - SCOPUS:85160228373
SN - 2041-1723
VL - 14
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 3020
ER -