Author
Listed:
- Dongsheng Jiang
(Helmholtz Zentrum München, Institute of Lung Biology and Disease, Group Regenerative Biology and Medicine)
- Simon Christ
(Helmholtz Zentrum München, Institute of Lung Biology and Disease, Group Regenerative Biology and Medicine)
- Donovan Correa-Gallegos
(Helmholtz Zentrum München, Institute of Lung Biology and Disease, Group Regenerative Biology and Medicine)
- Pushkar Ramesh
(Helmholtz Zentrum München, Institute of Lung Biology and Disease, Group Regenerative Biology and Medicine)
- Shruthi Kalgudde Gopal
(Helmholtz Zentrum München, Institute of Lung Biology and Disease, Group Regenerative Biology and Medicine)
- Juliane Wannemacher
(Helmholtz Zentrum München, Institute of Lung Biology and Disease, Group Regenerative Biology and Medicine)
- Christoph H. Mayr
(Helmholtz Zentrum München, Institute of Lung Biology and Disease, Group Systems Medicine of Chronic Lung Disease)
- Valerio Lupperger
(Helmholtz Zentrum München, Institute of Computational Biology)
- Qing Yu
(Helmholtz Zentrum München, Institute of Lung Biology and Disease, Group Regenerative Biology and Medicine)
- Haifeng Ye
(Helmholtz Zentrum München, Institute of Lung Biology and Disease, Group Regenerative Biology and Medicine)
- Martin Mück-Häusl
(Helmholtz Zentrum München, Institute of Lung Biology and Disease, Group Regenerative Biology and Medicine)
- Vijayanand Rajendran
(Helmholtz Zentrum München, Institute of Lung Biology and Disease, Group Regenerative Biology and Medicine)
- Li Wan
(Helmholtz Zentrum München, Institute of Lung Biology and Disease, Group Regenerative Biology and Medicine)
- Juan Liu
(Helmholtz Zentrum München, Institute of Lung Biology and Disease, Group Regenerative Biology and Medicine)
- Ursula Mirastschijski
(Mira-Beau gender esthetics
University of Bremen)
- Thomas Volz
(Technical University of Munich, School of Medicine, Klinikum rechts der Isar)
- Carsten Marr
(Helmholtz Zentrum München, Institute of Computational Biology)
- Herbert B. Schiller
(Helmholtz Zentrum München, Institute of Lung Biology and Disease, Group Systems Medicine of Chronic Lung Disease
German Centre for Lung Research (DZL))
- Yuval Rinkevich
(Helmholtz Zentrum München, Institute of Lung Biology and Disease, Group Regenerative Biology and Medicine
German Centre for Lung Research (DZL))
Abstract
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.
Suggested Citation
Dongsheng Jiang & Simon Christ & Donovan Correa-Gallegos & Pushkar Ramesh & Shruthi Kalgudde Gopal & Juliane Wannemacher & Christoph H. Mayr & Valerio Lupperger & Qing Yu & Haifeng Ye & Martin Mück-Hä, 2020.
"Injury triggers fascia fibroblast collective cell migration to drive scar formation through N-cadherin,"
Nature Communications, Nature, vol. 11(1), pages 1-13, December.
Handle:
RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-19425-1
DOI: 10.1038/s41467-020-19425-1
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