Mitogen- and ultraviolet-B-induced signaling pathways in normal human melanocytes

J Invest Dermatol. 2002 Feb;118(2):316-22. doi: 10.1046/j.0022-202x.2001.01694.x.

Abstract

In normal human melanocytes various mitogens activate the mitogen-activated protein kinases ERK1/2 and the downstream transcription factor CREB (Ca2+/cAMP response element binding protein). Endothelin-1, basic fibroblast growth factor, and alpha-melanotropin interact synergistically to stimulate human melanocyte proliferation. The former two mitogens phosphorylated ERK1/2, its substrate p90rsk, and CREB. Alpha-melanotropin, forskolin, or dibutyryl cAMP failed to phosphorylate any of those targets, however. The concomitant presence of endothelin-1, basic fibroblast growth factor, and alpha-melanotropin significantly potentiated CREB phosphorylation. The mitogen-induced phosphorylation of p90rsk and CREB was dependent on ERK1/2 activation, and was mediated by intracellular calcium mobilization and by protein kinase C and tyrosine kinase activation, but not by activation of the cAMP-dependent protein kinase A. Exposure of melanocytes to ultraviolet radiation B resulted in the phosphorylation of the stress-induced mitogen- activated protein kinases p38 and JNK/SAPK, but not ERK1/2. Ultraviolet radiation B induced the phosphorylation of CREB via a pathway that was partially dependent on p38, but had no effect on p90rsk or ERK1/2. Therefore, in human melanocytes, CREB is a common downstream target for distinct effectors that are involved in either mitogenic signaling or stress signaling initiated by ultraviolet radiation B.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Calcium / metabolism
  • Cells, Cultured
  • Cyclic AMP / metabolism
  • Cyclic AMP Response Element-Binding Protein / metabolism
  • Enzyme Activation / physiology
  • Humans
  • Intracellular Membranes / metabolism
  • Melanocytes / drug effects*
  • Melanocytes / physiology
  • Melanocytes / radiation effects*
  • Mitogen-Activated Protein Kinases / metabolism
  • Mitogens / pharmacology*
  • Osmolar Concentration
  • Phosphorylation / drug effects
  • Phosphorylation / radiation effects
  • Protein Kinase C / physiology
  • Protein-Tyrosine Kinases / physiology
  • Reference Values
  • Ribosomal Protein S6 Kinases / metabolism
  • Signal Transduction / physiology*
  • Ultraviolet Rays*

Substances

  • Cyclic AMP Response Element-Binding Protein
  • Mitogens
  • Cyclic AMP
  • Protein-Tyrosine Kinases
  • Ribosomal Protein S6 Kinases
  • Protein Kinase C
  • Mitogen-Activated Protein Kinases
  • Calcium