Organelle selection determines agonist-specific Ca2+ signals in pancreatic acinar and β cells

被引:166
|
作者
Yamasaki, M
Masgrau, R
Morgan, AJ
Churchill, GC
Patel, S
Ashcroft, SJH
Galione, A
机构
[1] Univ Oxford, Dept Pharmacol, Oxford OX1 3QT, England
[2] UCL, Dept Physiol, London WC1E 6BT, England
[3] Churchill Hosp, Oxford Ctr Diabet Endocrinol & Metab, Oxford OX3 7LJ, England
关键词
D O I
10.1074/jbc.M311088200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
How different extracellular stimuli can evoke different spatiotemporal Ca2+ signals is uncertain. We have elucidated a novel paradigm whereby different agonists use different Ca2+-storing organelles ("organelle seleetion") to evoke unique responses. Some agonists select the endoplasmic reticulum (ER), and others select lysosome-related (acidic) organelles, evoking spatial Ca2+ responses that mirror the organellar distribution. In pancreatic acinar cells, acetylcholine and bombesin exclusively select the ER Ca2+ store, whereas cholecystokinin additionally recruits a lysosome-related organelle. Similarly, in a pancreatic beta cell line MIN6, acetylcholine selects only the ER, whereas glucose mobilizes Ca2+ from a lysosome-related organelle. We also show that the key to organelle selection is the agonist-specific coupling messenger(s) such that the ER is selected by recruitment of inositol 1,4,5-trisphosphate (or cADP-ribose), whereas lysosome-related organelles are selected by NAADP.
引用
收藏
页码:7234 / 7240
页数:7
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