Expression of peroxisome proliferator-activated receptor and CCAAT/enhancer binding protein transcription factors in cultured human sebocytes

J Invest Dermatol. 2003 Sep;121(3):441-7. doi: 10.1046/j.1523-1747.2003.12411.x.

Abstract

Lipid synthesis and accumulation represent a major step in sebocyte differentiation and it may be of importance for sebocytes to express two families of transcription factors, CCAAT/enhancer binding proteins (c/EBPs) and peroxisome proliferator-activated receptors (PPARs), which were found to play a crucial role in the differentiation of adipocytes. Using the immortalized human sebaceous gland cell line SZ95 we examined the expression of the molecules before and after treatment with testosterone, 5alpha-dihydrotestosterone, dexamethasone, 17beta-estradiol and genistein, at 6, 12, 24, and 48 h, respectively. Reverse transcription-PCR analysis showed expression of peroxisome proliferator-activated receptors -alpha, -delta, -gamma1, -gamma2 and CCAAT/enhancer binding proteins-alpha, -beta, -gamma-delta in native SZ95 sebocytes. In western blot studies, high levels of CCAAT/enhancer binding proteins-alpha and -beta, and peroxisome proliferator-activated receptors-gamma were expressed at 6, 24, and 12 h, respectively. Immunostaining of the cultured sebocytes showed the CCAAT/enhancer binding proteins-alpha and -beta mainly localized within nuclei, whereas peroxisome proliferator-activated receptors-gamma in the cytoplasm. Strong staining of sebocytes was immunohistochemically revealed in the basal layer of sebaceous glands in human scalp and sebaceous nevus. Genistein down-regulated the expression of CCAAT/enhancer binding proteins-alpha and -beta, and peroxisome proliferator-activated receptors-gamma on the protein level. Treatment with linoleic acid for 48 h induced further differentiation of sebocytes leading to abundant lipid synthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / pharmacology
  • CCAAT-Enhancer-Binding Protein-alpha / genetics
  • CCAAT-Enhancer-Binding Protein-beta / genetics
  • CCAAT-Enhancer-Binding Protein-delta
  • CCAAT-Enhancer-Binding Proteins / genetics*
  • Cell Differentiation / physiology
  • Cell Line, Transformed
  • Dexamethasone / pharmacology
  • Dihydrotestosterone / pharmacology
  • Estrogens / pharmacology
  • Gene Expression / drug effects
  • Gene Expression / physiology
  • Genistein / pharmacology
  • Glucocorticoids / pharmacology
  • Gonadal Steroid Hormones / pharmacology
  • Humans
  • RNA, Messenger / analysis
  • Receptors, Cytoplasmic and Nuclear / genetics*
  • Sebaceous Glands / cytology*
  • Testosterone / pharmacology
  • Transcription Factors / genetics*

Substances

  • Antineoplastic Agents
  • CCAAT-Enhancer-Binding Protein-alpha
  • CCAAT-Enhancer-Binding Protein-beta
  • CCAAT-Enhancer-Binding Proteins
  • CCAAT-enhancer-binding protein-gamma
  • CEBPD protein, human
  • Estrogens
  • Glucocorticoids
  • Gonadal Steroid Hormones
  • RNA, Messenger
  • Receptors, Cytoplasmic and Nuclear
  • Transcription Factors
  • Dihydrotestosterone
  • CCAAT-Enhancer-Binding Protein-delta
  • Testosterone
  • Dexamethasone
  • Genistein