Science and Research

Two succeeding fibroblastic lineages drive dermal development and the transition from regeneration to scarring

During fetal development, mammalian back-skin undergoes a natural transition in response to injury, from scarless regeneration to skin scarring. Here, we characterize dermal morphogenesis and follow two distinct embryonic fibroblast lineages, based on their history of expression of the engrailed 1 gene. We use single-cell fate-mapping, live three dimensional confocal imaging and in silico analysis coupled with immunolabelling to reveal unanticipated structural and regional complexity and dynamics within the dermis. We show that dermal development and regeneration are driven by engrailed 1-history-naive fibroblasts, whose numbers subsequently decline. Conversely, engrailed 1-history-positive fibroblasts possess scarring abilities at this early stage and their expansion later on drives scar emergence. The transition can be reversed, locally, by transplanting engrailed 1-naive cells. Thus, fibroblastic lineage replacement couples the decline of regeneration with the emergence of scarring and creates potential clinical avenues to reduce scarring.

  • Jiang, D.
  • Correa-Gallegos, D.
  • Christ, S.
  • Stefanska, A.
  • Liu, J.
  • Ramesh, P.
  • Rajendran, V.
  • De Santis, M. M.
  • Wagner, D. E.
  • Rinkevich, Y.

Keywords

  • Animals
  • *Cell Lineage
  • Cell Movement
  • *Cell Proliferation
  • Cell Tracking
  • Cells, Cultured
  • Cicatrix/genetics/metabolism/*pathology
  • Disease Models, Animal
  • Fibroblasts/*metabolism/pathology/transplantation
  • Gene Expression Regulation, Developmental
  • Homeodomain Proteins/genetics/metabolism
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Microscopy, Confocal
  • Morphogenesis
  • Phenotype
  • *Regeneration
  • Signal Transduction
  • Single-Cell Analysis
  • Skin/injuries/*metabolism/pathology
  • Skin Transplantation
  • Time Factors
  • Wounds, Penetrating/genetics/metabolism/*pathology
Publication details
DOI: 10.1038/s41556-018-0073-8
Journal: Nature cell biology
Pages: 422-431 
Number: 4
Work Type: Original
Location: CPC-M
Disease Area: General Lung and Other
Partner / Member: HMGU
Access-Number: 29593327
See publication on PubMed


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