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Injury triggers fascia fibroblast collective cell migration to drive scar formation through N-cadherin

Scars are more severe when the subcutaneous fascia beneath the dermis is injured upon surgical or traumatic wounding. Here, we present a detailed analysis of fascia cell mobilisation by using deep tissue intravital live imaging of acute surgical wounds, fibroblast lineage-specific transgenic mice, a...

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Detalles Bibliográficos
Autores principales: Jiang, Dongsheng, Christ, Simon, Correa-Gallegos, Donovan, Ramesh, Pushkar, Kalgudde Gopal, Shruthi, Wannemacher, Juliane, Mayr, Christoph H., Lupperger, Valerio, Yu, Qing, Ye, Haifeng, Mück-Häusl, Martin, Rajendran, Vijayanand, Wan, Li, Liu, Juan, Mirastschijski, Ursula, Volz, Thomas, Marr, Carsten, Schiller, Herbert B., Rinkevich, Yuval
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7648088/
https://www.ncbi.nlm.nih.gov/pubmed/33159076
http://dx.doi.org/10.1038/s41467-020-19425-1
Descripción
Sumario:Scars are more severe when the subcutaneous fascia beneath the dermis is injured upon surgical or traumatic wounding. Here, we present a detailed analysis of fascia cell mobilisation by using deep tissue intravital live imaging of acute surgical wounds, fibroblast lineage-specific transgenic mice, and skin-fascia explants (scar-like tissue in a dish – SCAD). We observe that injury triggers a swarming-like collective cell migration of fascia fibroblasts that progressively contracts the skin and form scars. Swarming is exclusive to fascia fibroblasts, and requires the upregulation of N-cadherin. Both swarming and N-cadherin expression are absent from fibroblasts in the upper skin layers and the oral mucosa, tissues that repair wounds with minimal scar. Impeding N-cadherin binding inhibits swarming and skin contraction, and leads to reduced scarring in SCADs and in animals. Fibroblast swarming and N-cadherin thus provide therapeutic avenues to curtail fascia mobilisation and pathological fibrotic responses across a range of medical settings.