Enhanced insulin sensitivity in mice lacking ganglioside GM3

被引:437
作者
Yamashita, T
Hashiramoto, A
Haluzik, M
Mizukami, H
Beck, S
Norton, A
Kono, M
Tsuji, S
Daniotti, JL
Werth, N
Sandhoff, R
Sandhoff, K
Proia, RL
机构
[1] NIDDKD, Genet Dev & Dis Branch, NIH, Bethesda, MD 20892 USA
[2] NIDDKD, Diabet Branch, NIH, Bethesda, MD 20892 USA
[3] Ochanomizu Univ, Glycosci Inst, Bunkyo Ku, Tokyo 1128610, Japan
[4] Univ Nacl Cordoba, Fac Ciencias Quim, Dept Quim Biol, Ctr Invest Quim Biol Cordoba, RA-5000 Cordoba, Argentina
[5] Univ Bonn, Kekule Inst Organ Chem & Biochem, D-53121 Bonn, Germany
[6] Deutsch Krebsforschungszentrum, Abt Zellulare & Mol Pathol, D-69120 Heidelberg, Germany
关键词
D O I
10.1073/pnas.0635898100
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
Gangliosides are sialic acid-containing glycosphingolipids that are present on all mammalian plasma membranes where they participate in recognition and signaling activities. We have established mutant mice that lack GM3 synthase (CMP-NeuAc:lactosylceramide alpha2,3-sialyltransferase; EC 2.4.99.-). These mutant mice were unable to synthesize GM3 ganglioside, a simple and widely distributed glycosphingolipid. The mutant mice were viable and appeared without major abnormalities but showed a heightened sensitivity to insulin. A basis for the increased insulin sensitivity in the mutant mice was found to be enhanced insulin receptor phosphorylation in skeletal muscle. Importantly, the mutant mice were protected from high-fat diet-induced insulin resistance. Our results show that GM3 ganglioside is a negative regulator of insulin signaling, making it a potential therapeutic target in type 2 diabetes.
引用
收藏
页码:3445 / 3449
页数:5
相关论文
共 20 条
[1]   Lubricating cell signaling pathways with gangliosides [J].
Allende, ML ;
Proia, RL .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 2002, 12 (05) :587-592
[2]   The caveolae membrane system [J].
Anderson, RGW .
ANNUAL REVIEW OF BIOCHEMISTRY, 1998, 67 :199-225
[3]   The glycosynapse [J].
Hakomori, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (01) :225-232
[4]   Traveling for the glycosphingolipid path [J].
Hakomori, S .
GLYCOCONJUGATE JOURNAL, 2000, 17 (7-9) :627-647
[5]   Adrenalectomy improves diabetes in A-ZIP/F-1 lipoatrophic mice by increasing both liver and muscle insulin sensitivity [J].
Haluzik, M ;
Dietz, KR ;
Kim, JK ;
Marcus-Samuels, B ;
Shulman, GI ;
Gavrilova, O ;
Reitman, ML .
DIABETES, 2002, 51 (07) :2113-2118
[6]  
Kim BI, 2000, MAX PLANCK SERIES, V1, P105
[7]   Combinatorial ganglioside biosynthesis. [J].
Kolter, T ;
Proia, RL ;
Sandhoff, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (29) :25859-25862
[8]   A genetic model of substrate deprivation therapy for a glycosphingolipid storage disorder [J].
Liu, YJ ;
Wada, R ;
Kawai, H ;
Sango, K ;
Deng, CX ;
Tai, T ;
McDonald, MP ;
Araujo, K ;
Crawley, JN ;
Bierfreund, U ;
Sandhoff, K ;
Suzuki, K ;
Proia, RL .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (04) :497-505
[9]  
MILJAN EA, 2002, SCI STKE, pRE15
[10]   Potential role of TNF-α in the pathogenesis of insulin resistance and type 2 diabetes [J].
Moller, DE .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2000, 11 (06) :212-217