ob gene expression and secretion of leptin following differentiation of rat preadipocytes to adipocytes in primary culture

被引:56
|
作者
Mitchell, SE
Rees, WD
Hardie, LJ
Hoggard, N
Tadayyon, M
Arch, JRS
Trayhurn, P
机构
[1] ROWETT RES INST, DIV BIOCHEM SCI, MOL PHYSIOL GRP, BUCKSBURN AB21 9SB, ABERDEEN, SCOTLAND
[2] ROWETT RES INST, FETAL PROGRAMMING GRP, BUCKSBURN AB21 9SB, ABERDEEN, SCOTLAND
[3] SMITHKLINE BEECHAM PHARMACEUT, WELWYN GARDEN CITY AL6 9AR, HERTS, ENGLAND
关键词
D O I
10.1006/bbrc.1996.5964
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Expression of the ob gene and production of leptin have been examined on differentiation of rat fibroblastic preadipocytes to adipocytes in primary culture. Preadipocytes were obtained from the inguinal fat pad of suckling rats, and following differentiation the cells contained lipid droplets and the mRNAs for both lipoprotein lipase and adipsin were detected by Northern blotting. ob mRNA was not, however, detected on Northern blots, but analysis by RT-PCR indicated that the ob gene was expressed, particularly after differentiation. Measurement of leptin in the culture medium by ELISA showed that the ob gene product was secreted by adipocytes from approximately 4 days after the induction of differentiation. Leptin production was sustained over a a-week period with a peak at 8-10 days post-induction. Dexamethasone stimulated leptin production, while an inhibition was observed with the beta-adrenoceptor agonist isoprenaline. These results demonstrate that following the differentiation of fibroblastic preadipocytes to adipocytes in primary culture, leptin is secreted with the cells responding to stimuli which regulate production of the hormone. (C) 1997 Academic Press
引用
收藏
页码:360 / 364
页数:5
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