Stem Cell Factor Regulates Human Melanocyte‐Matrix Interactions

GLYNIS SCOTT, JAMES EWING, DANIEL RYAN, CAMILLE ABBOUD

Research output: Contribution to journalArticle

39 Scopus citations

Abstract

Stem cell factor (SCF) is hypothesized to play a critical role in the migration of melanocytes during embryogenesis because mutations in either the SCF gene, or its ligand, c‐kit, result in defects in coat pigmentation in mice and in skin pigmentation in humans. In this report we directly show that SCF alters the adhesion and migration of human melanocytes to extracellular matrix (ECM) ligands and regulates integrin expression at the protein level. SCF decreased adhesion of neonatal and fetal cells to collagen IV, and increased attachment of fetal cells to laminin. Attachment of fetal cells to fibronectin was decreased, but was unchanged in neonatal cells. Flow cytometry analysis of neonatal melanocytes showed that SCF down‐regulated the expression of the α2 receptor, and up‐regulated the expression of the α3, α5 and β1 integrin receptors. SCF down‐regulated expression of α2, α5 and β1 integrins by fetal melanocytes, and up‐regulated expression of the αv and α3 integrin receptors. Analysis of melanocyte migration using time‐lapse videomicroscopy showed that SCF significantly increased migration of neonatal, but not fetal, melanocytes on fibronectin (FN). We conclude that SCF regulates integrin expression at the protein level and that SCF has pleiotropic effects on melanocyte attachment and migration on ECM ligands. We suggest that this may be one mechanism by which SCF regulates melanocyte migration during development of the skin.

Original languageEnglish
Pages (from-to)44-51
Number of pages8
JournalPigment Cell Research
Volume7
Issue number1
DOIs
StatePublished - Feb 1994
Externally publishedYes

Keywords

  • Extracellular matrix
  • Neural crest cells
  • Tyrosine‐kinase receptor

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