TY - JOUR
T1 - Expression of peroxisome proliferator-activated receptor and CCAAT/ enhancer binding protein transcription factors in cultured human sebocytes
AU - Chen, Wen Chieh
AU - Yang, Chao Chun
AU - Sheu, Hamm Ming
AU - Seltmann, Holger
AU - Zouboulis, Christos C.
N1 - Funding Information:
The work was financially supported by a grant from National Science Council Taiwan (NSC 89-2314-B-006-096). H.S. was supported by a grant from the Bundesinstitut für gesundheitlichen Verbraucherschutz und Veterinärmedizin to Ch.C.Z. (BgVV Z 5.1-1328-156). The authors wish to thank Prof. R. Rosenfield (The University of Chicago Hospital, USA) and Dr M Philpott (Queen Marys School of Medicine and Dentistry, UK) for critical review of the manuscript. We also thank Wen-Chuan Hsieh, Ya-Nan Chang, Chia-Chie Chiu, and Anna Schnitger for excellent technical assistance.
PY - 2003/9/1
Y1 - 2003/9/1
N2 - 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, 5α-dihydrotestosterone, dexamethasone, 17β-estradiol and genistein, at 6, 12, 24, and 48 h, respectively. Reverse transcription-PCR analysis showed expression of peroxisome proliferator-activated receptors -α, -δ, -γ1, -γ2 and CCAAT/enhancer binding proteins-α, -β, -γ -δ in native SZ95 sebocytes. In western blot studies, high levels of CCAAT/enhancer binding proteins-α and -β, and peroxisome proliferator-activated receptors-γ were expressed at 6, 24, and 12 h, respectively. Immunostaining of the cultured sebocytes showed the CCAAT/ enhancer binding proteins-α and -β mainly localized within nuclei, whereas peroxisome proliferator-activated receptors-γ 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-α and -β, and peroxisome proliferator-activated receptors-γ on the protein level. Treatment with linoleic acid for 48 h induced further differentiation of sebocytes leading to abundant lipid synthesis.
AB - 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, 5α-dihydrotestosterone, dexamethasone, 17β-estradiol and genistein, at 6, 12, 24, and 48 h, respectively. Reverse transcription-PCR analysis showed expression of peroxisome proliferator-activated receptors -α, -δ, -γ1, -γ2 and CCAAT/enhancer binding proteins-α, -β, -γ -δ in native SZ95 sebocytes. In western blot studies, high levels of CCAAT/enhancer binding proteins-α and -β, and peroxisome proliferator-activated receptors-γ were expressed at 6, 24, and 12 h, respectively. Immunostaining of the cultured sebocytes showed the CCAAT/ enhancer binding proteins-α and -β mainly localized within nuclei, whereas peroxisome proliferator-activated receptors-γ 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-α and -β, and peroxisome proliferator-activated receptors-γ on the protein level. Treatment with linoleic acid for 48 h induced further differentiation of sebocytes leading to abundant lipid synthesis.
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U2 - 10.1046/j.1523-1747.2003.12411.x
DO - 10.1046/j.1523-1747.2003.12411.x
M3 - Article
C2 - 12925198
AN - SCOPUS:0042334918
VL - 121
SP - 441
EP - 447
JO - Journal of Investigative Dermatology
JF - Journal of Investigative Dermatology
SN - 0022-202X
IS - 3
ER -