REGULATED EXPRESSION OF THE OBESE GENE-PRODUCT (LEPTIN) IN WHITE ADIPOSE-TISSUE AND 3T3-L1 ADIPOCYTES

被引:476
作者
MACDOUGALD, OA
HWANG, CS
FAN, HY
LANE, MD
机构
[1] Department of Biological Chemistry, Johns Hopkins Univ. Sch. of Medicine, Baltimore
关键词
OBESITY; PROTEIN SECRETION; OB LOCUS; CCAAT; ENHANCER-BINDING PROTEIN; PREADIPOCYTE DIFFERENTIATION;
D O I
10.1073/pnas.92.20.9034
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A mutation within the obese gene was recently identified as the genetic basis for obesity in the ob/ob mouse, The obese gene product, leptin, is a 16-kDa protein expressed predominantly in adipose tissue, Consistent with leptin's postulated role as an extracellular signaling protein, human embryonic kidney 293 cells transfected with the obese gene secreted leptin with minimal intracellular accumulation. Upon differentiation of 3T3-L1 preadipocytes into adipocytes, the leptin mRNA aas expressed concomitant with mRNAs encoding adipocyte marker proteins, A factor(s) present in calf serum markedly activated expression of leptin by fully differentiated 3T3-L1 adipocytes. A 16-hr fast decreased (by approximate to 85%) the leptin mRNA level of adipose tissue of lean (ob/ + or +/+) mice but had no effect on the approximate to 4-fold higher level in obese (ob/ob) littermates. Since the mutation at the ob locus fails to produce the functional protein, yet its cognate mRNA is overproduced, it appears that leptin is necessary for its own downregulation, Leptin mRNA was also suppressed in adipose tissue of rats during a 16-hr fast and was rapidly induced during a 4-hr refeeding period. Insulin deficiency provoked by streptozotocin also markedly down-regulated leptin mRNA add this suppression was rapidly reversed by insulin, These results suggest that insulin may regulate the expression of leptin.
引用
收藏
页码:9034 / 9037
页数:4
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