Two endogenous gonadotropin-releasing hormones generate dissimilar Ca2+ signals in identified goldfish gonadotropes

被引:39
作者
Johnson, JD [1 ]
Van Goor, F [1 ]
Wong, CJH [1 ]
Goldberg, JI [1 ]
Chang, JP [1 ]
机构
[1] Univ Alberta, Dept Sci Biol, Edmonton, AB T6G 2E9, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
pituitary; neuroendocrine; Fura-2; imaging; gonadotropin; neuropeptide; secretion; coding; spatial calcium signals;
D O I
10.1006/gcen.1999.7349
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Ca2+ signals are involved in the signal transduction of neuroendocrine regulators. In goldfish, two endogenous gonadotropin-releasing hormones, salmon (s)GnRH and chicken (c)GnRH-II, control maturational gonadotropin secretion. Although considerable evidence suggests that sGnRH and cGnRH-II exert their activity on goldfish gonadotropes through a single population of receptors, differences in signal transduction mechanisms between these peptides have been demonstrated. We used ratio-metric Fura-2 Ca2+ imaging of single morphologically identified gonadotropes to quantitatively compare the Ca2+ signals evoked by sGnRH and cGnRH-II. The amplitude and the rate of rise of sGnRH- and cGnRH-II-evoked Ca2+ signals increased with concentration. At maximal concentrations, Ca2+ signals generated by cGnRH-II rose significantly faster than those elicited by sGnRH, while other parameters such as the maximum amplitude, average Ca2+ increase, and latency did not differ between the two peptides. Ca2+ signals evoked by sGnRH or cGnRH-II were often spatially restricted to one part of the cell over the duration of the response. We provide a comprehensive account of the spatial and temporal aspects, including calculated kinetics, of GnRH-evoked Ca2+ signals in single identified gonadotropes. This is the first report of quantified differences in Ca2+ signals generated by two endogenous GnRH neuropeptides, which may act through the same receptor population in this cell type. (C) 1999 Academic Press.
引用
收藏
页码:178 / 191
页数:14
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