Retinoic acid upregulates c-kit ligand production by murine keratinocyte in vitro and increases cutaneous mast cell in vivo

J Dermatol Sci. 1995 Jan;9(1):27-35. doi: 10.1016/0923-1811(94)00349-j.

Abstract

Mouse-transformed epidermal cell line (Pam 212) generated the soluble mediators for promoting the growth of a mast cell line (MC9) in the presence of retinoic acid at a concentration of 10(-6)-10(-7) M. The effective molecule of MC9 cell growth promoting factor (MC9-GF) was non-dialyzable and eluted between the molecular weight of 45 K and 68 K on a TSK 2000 G column. Chromatofocusing analysis revealed that this factor had a pI range between 7.0 and 7.5. Anti-c-kit ligand antibody abrogated MC9-GF activity and RT-PCR analysis demonstrated that retinoic acid upregulates c-kit ligand mRNA expression by Pam cells. Several recombinant cytokines including IL1-alpha, IL-1 beta, IL-2, IL-3 or IL-4 did not promote MC9 cell growth at a concentration of 100 U/ml. The presence of anti-IL-1 alpha, -IL-1 beta, -IL-2, -IL-3 or -IL-4 antibodies did not abrogate the MC9-GF activity except for anti-c-kit ligand antibody.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Cell Line
  • Cytokines / pharmacology
  • DNA / genetics
  • Growth Substances / biosynthesis
  • Hyperplasia
  • In Vitro Techniques
  • Keratinocytes / drug effects*
  • Keratinocytes / metabolism*
  • Mast Cells / drug effects
  • Mast Cells / pathology
  • Mice
  • Mice, Inbred BALB C
  • Molecular Sequence Data
  • Polymerase Chain Reaction
  • Proto-Oncogene Proteins / biosynthesis*
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins c-kit
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptor Protein-Tyrosine Kinases / biosynthesis*
  • Receptor Protein-Tyrosine Kinases / genetics
  • Receptors, Colony-Stimulating Factor / biosynthesis*
  • Receptors, Colony-Stimulating Factor / genetics
  • Skin / drug effects
  • Skin / pathology
  • Tretinoin / pharmacology*
  • Up-Regulation / drug effects

Substances

  • Cytokines
  • Growth Substances
  • Proto-Oncogene Proteins
  • RNA, Messenger
  • Receptors, Colony-Stimulating Factor
  • Tretinoin
  • DNA
  • Proto-Oncogene Proteins c-kit
  • Receptor Protein-Tyrosine Kinases