Keystone meeting summary: 'Adipogenesis, obesity, and inflammation' and 'Diabetes mellitus and the control of cellular energy metabolism,' January 21-26, 2006, Vancouver, Canada

被引:6
作者
Corvera, Silvia [1 ]
Burkart, Alison
Kim, Ja-Young
Christianson, Jennifer
Wang, Zhao
Scherer, Philipp E.
机构
[1] Univ Massachusetts, Program Mol Med, Sch Med, Worcester, MA 01605 USA
[2] Albert Einstein Coll Med, Dept Cell Biol, Bronx, NY 10461 USA
[3] Yeshiva Univ Albert Einstein Coll Med, Dept Med, Bronx, NY 10461 USA
[4] Yeshiva Univ Albert Einstein Coll Med, Dept Diabet Res, Bronx, NY 10461 USA
[5] Yeshiva Univ Albert Einstein Coll Med, Training Ctr, Bronx, NY 10461 USA
关键词
diabetes; adipocyte; inflammation; mitochondria; ER stress;
D O I
10.1101/gad.1447506
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The dysregulation of specific cellular functions in adipocytes, muscle cells, beta cells, and the liver leads to changes in systemic metabolic processes and ultimately to the pathophysiological manifestations that cause type 2 diabetes. The underlying cellular mechanisms are complex. The two meetings summarized here aimed to highlight the recent advances in our understanding of the molecular basis of feeding and nutrient storage and on the molecular consequences of obesity in terms of promoting risk for type 2 diabetes and cardiovascular disease.
引用
收藏
页码:2193 / 2201
页数:9
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