The islet β-cell: fuel responsive and vulnerable

被引:121
作者
Nolan, Christopher J. [1 ,2 ]
Prentki, Marc [3 ,4 ,5 ]
机构
[1] Australian Natl Univ, Dept Endocrinol, Canberra Hosp, Garran, ACT 2605, Australia
[2] Australian Natl Univ, Sch Med, Garran, ACT 2605, Australia
[3] Univ Montreal, Mol Nutr Unit, Montreal, PQ H1W 4A4, Canada
[4] Univ Montreal, Montreal Diabet Res Ctr, Montreal, PQ H1W 4A4, Canada
[5] CRCHUM, Montreal, PQ H1W 4A4, Canada
关键词
D O I
10.1016/j.tem.2008.07.006
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
The pancreatic P-cell senses blood nutrient levels and is modulated by neurohormonal signals so that it secretes insulin according to the need of the organism. Nutrient sensing involves marked metabolic activation, resulting in the production of coupling signals that promote insulin biosynthesis and secretion. The P-cell's high capacity for nutrient sensing, however, necessitates reduced protection to nutrient toxicity. This potentially explains why in susceptible individuals, chronic fuel surfeit results in beta-cell failure and type 2 diabetes. Here we discuss recent insights into first, the biochemical basis of P-cell signaling in response to glucose, amino acids and fatty acids, and second, P-cell nutrient detoxification. We emphasize the emerging role of glycerolipid/fatty acid cycling in these processes.
引用
收藏
页码:285 / 291
页数:7
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