Migration of melanoblasts into the developing murine hair follicle is accompanied by transient c-Kit expression

J Histochem Cytochem. 2002 Jun;50(6):751-66. doi: 10.1177/002215540205000602.

Abstract

Disruption of the c-Kit/stem cell factor (SCF) signaling pathway interferes with the survival, migration, and differentiation of melanocytes during generation of the hair follicle pigmentary unit. We examined c-Kit, SCF, and S100 (a marker for precursor melanocytic cells) expression, as well as melanoblast/melanocyte ultrastructure, in perinatal C57BL/6 mouse skin. Before the onset of hair bulb melanogenesis (i.e., stages 0-4 of hair follicle morphogenesis), strong c-Kit immunoreactivity (IR) was seen in selected non-melanogenic cells in the developing hair placode and hair plug. Many of these cells were S100-IR and were ultrastructurally identified as melanoblasts with migratory appearance. During the subsequent stages (5 and 6), increasingly dendritic c-Kit-IR cells successively invaded the hair bulb, while S100-IR gradually disappeared from these cells. Towards the completion of hair follicle morphogenesis (stages 7 and 8), several distinct follicular melanocytic cell populations could be defined and consisted broadly of (a) undifferentiated, non-pigmented c-Kit-negative melanoblasts in the outer root sheath and bulge and (b) highly differentiated melanocytes adjacent to the hair follicle dermal papilla above Auber's line. Widespread epithelial SCF-IR was seen throughout hair follicle morphogenesis. These findings suggest that melanoblasts express c-Kit as a prerequisite for migration into the SCF-supplying hair follicle epithelium. In addition, differentiated c-Kit-IR melanocytes target the bulb, while non-c-Kit-IR melanoblasts invade the outer root sheath and bulge in fully developed hair follicles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Cell Movement
  • Hair Follicle / embryology
  • Hair Follicle / physiology*
  • Hair Follicle / ultrastructure
  • Immunohistochemistry
  • Melanocytes / metabolism
  • Melanocytes / physiology*
  • Melanocytes / ultrastructure
  • Mice
  • Mice, Inbred C57BL
  • Microscopy, Electron
  • Morphogenesis
  • Stem Cell Factor / metabolism*
  • Stem Cells / metabolism
  • Stem Cells / physiology
  • Stem Cells / ultrastructure

Substances

  • Stem Cell Factor