α-lipoic acid inhibits adipocyte differentiation by regulating pro-adipogenic transcription factors via mitogen-activated protein kinase pathways

被引:73
作者
Cho, KJ
Moon, HE
Moini, H
Packer, L
Yoon, DY
Chung, AS
机构
[1] Korea Adv Inst Sci & Technol, Dept Biol Sci, Taejon 305701, South Korea
[2] Univ So Calif, Sch Pharm, Dept Mol Pharmacol & Toxicol, Los Angeles, CA 90089 USA
[3] Korea Inst Biosci & Biotechnol, Cell Biol Lab, Taejon 305333, South Korea
关键词
D O I
10.1074/jbc.M210747200
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
Obesity is associated with a number of pathological disorders such as non-insulin-dependent diabetes, hypertension, hyperlipidemia, and cardiovascular diseases. alpha-Lipoic acid (LA) has been demonstrated to activate the insulin signaling pathway and to exert insulin-like actions in adipose and muscle cells. Based on this similarity LA is expected to promote adipogenesis in pre-adipocytes. Here, however, we report that LA inhibited differentiation of 3T3-L1 pre-adipocytes induced by a hormonal mixture or troglitazone. Northern blot analysis of cells demonstrated that this inhibition was accompanied with attenuated expression of adipocyte-specific fatty acid-binding protein and lipoprotein lipase. Electrophoretic mobility shift assay and Western blot analysis of cells demonstrated that LA modulates transcriptional activity and/or expression of a set of anti- or pro-adipogenic transcription factors. LA treatment of 3T3-L1 pre-adipocytes also resulted in prolonged activation of major mitogen-activated protein kinase signaling pathways but showed little or no effect on the activity of the insulin receptor/Akt signaling pathway. These findings suggest that LA inhibits insulin or the hormonal mixture-induced differentiation of 3T3-L1 pre-adipocytes by modulating activity and/or expression of pro- or anti- adipogenic transcription factors mainly through activating the MAPK pathways.
引用
收藏
页码:34823 / 34833
页数:11
相关论文
共 40 条
[1]  
BERNLOHR DA, 1985, J BIOL CHEM, V260, P5563
[2]   Jun NH2-terminal kinase phosphorylation of p53 on Thr-81 is important for p53 stabilization and transcriptional activities in response to stress [J].
Buschmann, T ;
Potapova, O ;
Bar-Shira, A ;
Ivanov, VN ;
Fuchs, SY ;
Henderson, S ;
Fried, VA ;
Minamoto, T ;
Alarcon-Vargas, D ;
Pincus, MR ;
Gaarde, WA ;
Holbrook, NJ ;
Shiloh, Y ;
Ronai, Z .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (08) :2743-2754
[3]   c-Jun N-terminal kinase phosphorylates peroxisome proliferator-activated receptor-γ1 and negatively regulates its transcriptional activity [J].
Camp, HS ;
Tafuri, SR ;
Leff, T .
ENDOCRINOLOGY, 1999, 140 (01) :392-397
[4]  
Camp HS, 1997, J BIOL CHEM, V272, P10811
[5]   CELLULAR ALTERATIONS IN LIVER, SKELETAL-MUSCLE, AND ADIPOSE-TISSUE RESPONSIBLE FOR INSULIN RESISTANCE IN OBESITY AND TYPE-II DIABETES [J].
CARO, JF ;
DOHM, LG ;
PORIES, WJ ;
SINHA, MK .
DIABETES-METABOLISM REVIEWS, 1989, 5 (08) :665-689
[6]   Oxidant-mediated activation of mitogen-activated protein kinases and nuclear transcription factors in the cardiovascular system: A brief overview [J].
Chakraborti, S ;
Chakraborti, T .
CELLULAR SIGNALLING, 1998, 10 (10) :675-683
[7]   Effect of bioflavonoids extracted from the bark of Pinus maritima on proinflammatory cytokine interleukin-1 production in lipopolysaccharide-stimulated RAW 264.7 [J].
Cho, KJ ;
Yun, CH ;
Yoon, DY ;
Cho, YS ;
Rimbach, G ;
Packer, L ;
Chung, AS .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2000, 168 (01) :64-71
[8]   Mitogen- and stress-activated protein kinase-1 (MSK1) is directly activated by MAPK and SAPK2/p38, and may mediate activation of CREB [J].
Deak, M ;
Clifton, AD ;
Lucocq, JM ;
Alessi, DR .
EMBO JOURNAL, 1998, 17 (15) :4426-4441
[9]   Mitogen-activated protein kinase activation is not necessary for, but antagonizes, 3T3-L1 adipocytic differentiation [J].
deMora, JF ;
Porras, A ;
Ahn, N ;
Santos, E .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (10) :6068-6075
[10]   NUCLEOPROTEIN COMPLEXES THAT REGULATE GENE-EXPRESSION IN ADIPOCYTE DIFFERENTIATION - DIRECT PARTICIPATION OF C-FOS [J].
DISTEL, RJ ;
RO, HS ;
ROSEN, BS ;
GROVES, DL ;
SPIEGELMAN, BM .
CELL, 1987, 49 (06) :835-844