Stimulation of the proliferation and differentiation of mouse pink-eyed dilution epidermal melanocytes by excess tyrosine in serum-free primary culture

J Cell Physiol. 2002 May;191(2):162-72. doi: 10.1002/jcp.10085.

Abstract

The epidermal cell suspensions of the neonatal dorsal skin derived from wild type mouse at the pink-eyed dilution (p) locus (black, C57BL/10JHir-P/P) and their congenic mutant mouse (pink-eyed dilution, C57BL/10JHir-p/p) were cultured with a serum-free melanocyte growth medium supplemented with additional L-tyrosine (Tyr) from initiation of the primary culture. L-Tyr inhibited the proliferation of P/Pmelanocytes in a dose-dependent manner, whereas L-Tyr stimulated the proliferation of p/p melanoblasts and melanocytes regardless of dose. On the other hand, L-Tyr stimulated (P/P) or induced (p/p) the differentiation of epidermal melanocytes in a dose-dependent manner. In both P/P and p/p melanoblasts and melanocytes cultured with 2.0 mM L-Tyr for 14 days, slight increases in contents of eumelanin marker, pyrrole-2,3,5-tricarboxylic acid (PTCA) and pheomelanin marker, aminohydroxyphenylalanine (AHP) were observed. The average number of total melanosomes (stages I, II, III, and IV) per P/P melanocyte was not changed by L-Tyr treatment, but the proportion of stage IV melanosomes in the total melanosomes was increased. On the contrary, in p/p melanoblasts and melanocytes L-Tyr increased dramatically the number of stage II, III, and IV melanosomes as well as the proportion of stage III melanosomes. Contents of PTCA and eumelanin precursor, 5,6-dihydroxyindole-2-carboxylic acid (DHICA) of cultured media in p/p melanocytes were much more greatly increased than in P/P melanocytes. However, contents of AHP and pheomelanin precursor, 5-S-cysteinyldopa (5-S-CD) of cultured media in p/p melanocytes were increased in a similar tendency to P/Pmelanocytes. These results suggest that p/p melanocytes in the primary culture are induced to synthesize eumelanin by excess L-Tyr, but difficult to accumulate them in melanosomes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carrier Proteins*
  • Cell Differentiation / drug effects
  • Cell Differentiation / physiology*
  • Cell Division / drug effects
  • Cell Division / physiology*
  • Cells, Cultured
  • Culture Media, Serum-Free / pharmacology
  • Dihydroxyphenylalanine / analogs & derivatives*
  • Dihydroxyphenylalanine / metabolism
  • Dose-Response Relationship, Drug
  • Epidermis / drug effects
  • Epidermis / metabolism*
  • Epidermis / ultrastructure
  • Female
  • Indoles / metabolism
  • Male
  • Melanins / metabolism
  • Melanocytes / drug effects
  • Melanocytes / metabolism*
  • Melanocytes / ultrastructure
  • Membrane Glycoproteins*
  • Membrane Proteins / drug effects
  • Membrane Proteins / genetics*
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Inbred Strains
  • Monophenol Monooxygenase / metabolism
  • Oxidoreductases*
  • Proteins / metabolism
  • Proto-Oncogene Proteins c-kit / metabolism
  • Pyrroles / metabolism
  • Tyrosine / drug effects
  • Tyrosine / metabolism*

Substances

  • 5-S-cysteinyl-3,4-dihydroxyphenylalanine
  • Carrier Proteins
  • Culture Media, Serum-Free
  • Indoles
  • Melanins
  • Membrane Glycoproteins
  • Membrane Proteins
  • Proteins
  • Pyrroles
  • pheomelanin
  • P protein, mouse
  • Tyrosine
  • 5,6-dihydroxy-2-indolylcarboxylic acid
  • Dihydroxyphenylalanine
  • pyrrole-2,3,5-tricarboxylic acid
  • Oxidoreductases
  • Tyrp1 protein, mouse
  • tyrosinase-related protein-1
  • Monophenol Monooxygenase
  • Proto-Oncogene Proteins c-kit