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Endoplasmic Reticulum Stress and Inflammation in Obesity and Diabetes
被引:364
作者:

Hummasti, Sarah
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Publ Hlth, Dept Genet & Complex Dis, Boston, MA 02115 USA

Hotamisligil, Goekhan S.
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Publ Hlth, Dept Genet & Complex Dis, Boston, MA 02115 USA
机构:
[1] Harvard Univ, Sch Publ Hlth, Dept Genet & Complex Dis, Boston, MA 02115 USA
[2] Harvard Univ, Sch Publ Hlth, Dept Nutr, Boston, MA 02115 USA
[3] Broad Inst Harvard & Massachusetts Inst Technol, Boston, MA USA
关键词:
obesity;
ER stress;
inflammation;
UNFOLDED PROTEIN RESPONSE;
NECROSIS-FACTOR-ALPHA;
NF-KAPPA-B;
ADIPOSE-TISSUE INFLAMMATION;
SATURATED FATTY-ACIDS;
PANCREATIC BETA-CELL;
BODY-MASS INDEX;
INSULIN-RESISTANCE;
ER STRESS;
T-CELLS;
D O I:
10.1161/CIRCRESAHA.110.225698
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Obesity is a major problem worldwide that increases risk for a wide range of diseases, including diabetes and heart disease. As such, it is increasingly important to understand how excess adiposity can perturb normal metabolic functions. It is now clear that this disruption involves not only pathways controlling lipid and glucose homeostasis but also integration of metabolic and immune response pathways. Under conditions of nutritional excess, this integration can result in a metabolically driven, low-grade, chronic inflammatory state, referred to as "metaflammation," that targets metabolically critical organs and tissues to adversely affect systemic homeostasis. Endoplasmic reticulum dysfunction is another important feature of chronic metabolic disease that is also linked to both metabolic and immune regulation. A thorough understanding of how these pathways intersect to maintain metabolic homeostasis, as well as how this integration is altered under conditions of nutrient excess, is important to fully understand, and subsequently treat, chronic metabolic diseases. (Circ Res. 2010;107:579-591.)
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页码:579 / 591
页数:13
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