Glucose-mediated control of ghrelin release from primary cultures of gastric mucosal cells

被引:81
作者
Sakata, Ichiro [1 ,2 ]
Park, Won-Mee [1 ]
Walker, Angela K. [1 ]
Piper, Paul K. [3 ]
Chuang, Jen-Chieh [1 ]
Osborne-Lawrence, Sherri [1 ]
Zigman, Jeffrey M. [1 ,3 ,4 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Internal Med, Div Hypothalam Res, Dallas, TX 75390 USA
[2] Saitama Univ, Grad Sch Sci & Engn, Div Life Sci, Saitama 3388570, Japan
[3] Univ Texas SW Med Ctr Dallas, Div Endocrinol & Metab, Dept Internal Med, Dallas, TX 75390 USA
[4] Univ Texas SW Med Ctr Dallas, Dept Psychiat, Dallas, TX 75390 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2012年 / 302卷 / 10期
基金
美国国家卫生研究院;
关键词
secretion; INSULIN-SECRETION; BETA-CELLS; O-ACYLTRANSFERASE; ANOREXIA-NERVOSA; GLUCAGON-RELEASE; GLYCEMIC CONTROL; ALPHA-CELLS; K+ CHANNELS; HORMONE; MICE;
D O I
10.1152/ajpendo.00041.2012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Sakata I, Park WM, Walker AK, Piper PK, Chuang JC, Osborne-Lawrence S, Zigman JM. Glucose-mediated control of ghrelin release from primary cultures of gastric mucosal cells. Am J Physiol Endocrinol Metab 302: E1300-E1310, 2012. First published March 13, 2012; doi:10.1152/ajpendo.00041.2012.-The peptide hormone ghrelin is released from a distinct group of gastrointestinal cells in response to caloric restriction, whereas its levels fall after eating. The mechanisms by which ghrelin secretion is regulated remain largely unknown. Here, we have used primary cultures of mouse gastric mucosal cells to investigate ghrelin secretion, with an emphasis on the role of glucose. Ghrelin secretion from these cells upon exposure to different D-glucose concentrations, the glucose antimetabolite 2-deoxy-D-glucose, and other potential secretagogues was assessed. The expression profile of proteins involved in glucose transport, metabolism, and utilization within highly enriched pools of mouse ghrelin cells and within cultured ghrelinoma cells was also determined. Ghrelin release negatively correlated with D-glucose concentration. Insulin blocked ghrelin release, but only in a low D-glucose environment. 2-Deoxy-D-glucose prevented the inhibitory effect of high D-glucose exposure on ghrelin release. mRNAs encoding several facilitative glucose transporters, hexokinases, the ATP-sensitive potassium channel subunit Kir6.2, and sulfonylurea type 1 receptor were expressed highly within ghrelin cells, although neither tolbutamide nor diazoxide exerted direct effects on ghrelin secretion. These findings suggest that direct exposure of ghrelin cells to low ambient D-glucose stimulates ghrelin release, whereas high D-glucose and glucose metabolism within ghrelin cells block ghrelin release. Also, low D-glucose sensitizes ghrelin cells to insulin. Various glucose transporters, channels, and enzymes that mediate glucose responsiveness in other cell types may contribute to the ghrelin cell machinery involved in regulating ghrelin secretion under these different glucose environments, although their exact roles in ghrelin release remain uncertain.
引用
收藏
页码:E1300 / E1310
页数:11
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