Re-epithelialization of cutaneous wounds in adult zebrafish combines mechanisms of wound closure in embryonic and adult mammals

Development. 2016 Jun 15;143(12):2077-88. doi: 10.1242/dev.130492. Epub 2016 Apr 27.

Abstract

Re-epithelialization of cutaneous wounds in adult mammals takes days to complete and relies on numerous signalling cues and multiple overlapping cellular processes that take place both within the epidermis and in other participating tissues. Re-epithelialization of partial- or full-thickness skin wounds of adult zebrafish, however, is extremely rapid and largely independent of the other processes of wound healing. Live imaging after treatment with transgene-encoded or chemical inhibitors reveals that re-epithelializing keratinocytes repopulate wounds by TGF-β- and integrin-dependent lamellipodial crawling at the leading edges of the epidermal tongue. In addition, re-epithelialization requires long-range epithelial rearrangements, involving radial intercalations, flattening and directed elongation of cells - processes that are dependent on Rho kinase, JNK and, to some extent, planar cell polarity within the epidermis. These rearrangements lead to a massive recruitment of keratinocytes from the adjacent epidermis and make re-epithelialization independent of keratinocyte proliferation and the mitogenic effect of FGF signalling, which are only required after wound closure, allowing the epidermis outside the wound to re-establish its normal thickness. Together, these results demonstrate that the adult zebrafish is a valuable in vivo model for studying and visualizing the processes involved in cutaneous wound closure, facilitating the dissection of direct from indirect and motogenic from mitogenic effects of genes and molecules affecting wound re-epithelialization.

Keywords: Cell proliferation; FGF; Re-epithelialization; Skin; TGF-β; Wound healing.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actin Cytoskeleton / metabolism
  • Aging / physiology*
  • Animals
  • Cell Movement
  • Cell Proliferation
  • Embryo, Mammalian / physiology*
  • Epidermis / pathology
  • Epithelial Cells / metabolism
  • Fibroblast Growth Factors / metabolism
  • Integrins / metabolism
  • JNK Mitogen-Activated Protein Kinases / metabolism
  • Keratinocytes / pathology
  • Mammals / embryology*
  • Morphogenesis
  • Pseudopodia / metabolism
  • Re-Epithelialization*
  • Signal Transduction
  • Skin / pathology*
  • Transforming Growth Factor beta / metabolism
  • Zebrafish / physiology*
  • rho-Associated Kinases / metabolism

Substances

  • Integrins
  • Transforming Growth Factor beta
  • Fibroblast Growth Factors
  • rho-Associated Kinases
  • JNK Mitogen-Activated Protein Kinases