Misoprostol elevates intracellular calcium in Neuro-2a cells via protein kinase A

被引:14
|
作者
Tamiji, Javaneh [2 ,3 ]
Crawford, Dorota A. [1 ,2 ,3 ]
机构
[1] York Univ, Fac Hlth, Bethune Coll, Dept Biol, Toronto, ON M3J 1P3, Canada
[2] York Univ, Sch Kinesiol & Hlth Sci, Toronto, ON M3J 1P3, Canada
[3] York Univ, Neurosci Grad Diploma Program, Toronto, ON M3J 1P3, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Misoprostol; Prostaglandin E-2; Calcium; Fura-2; AM; Protein kinase A; Neuro-2a cell; PROSTANOID RECEPTORS; PROSTAGLANDIN E-2; EP3; RECEPTORS; CA2+ RELEASE; CAMP; PHARMACOLOGY; EXPRESSION; ACTIVATION; PREGNANCY; SUBTYPES;
D O I
10.1016/j.bbrc.2010.07.112
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
Misoprostol, a prostaglandin type E analogue, has been implicated in a number of neurodevelopmental disorders. However, its mode of action in the nervous system is not well understood. Misoprostol acts on the same receptors as prostaglandin E-2 (PGE(2)), a natural lipid-derived compound, which mediates important physiological functions in the nervous system via activation of four EP receptors (EP1-4). In this study we use a ratiometric calcium imaging with fura-2 AM as a calcium indicator to show that misoprostol alters intracellular calcium levels in mouse neuroblastoma (Neuro-2a) cells via similar mechanisms as PGE(2). We demonstrate that the misoprostol-induced increase in calcium is mediated by a protein kinase A (PKA)-dependent mechanism and that the EP4 receptor signaling pathway may play an inhibitory role on calcium regulation. Overall, this study provides further support for the involvement of PGE(2) signaling in calcium homeostasis and suggests its important role in the nervous system. Crown Copyright (C) 2010 Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:565 / 570
页数:6
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