کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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2801276 | 1156151 | 2010 | 7 صفحه PDF | دانلود رایگان |
Pituitary melanotrope cells of the amphibian Xenopus laevis are neuroendocrine cells regulating the animal’s skin color adaptation through secretion of α-melanophore-stimulating hormone (α-MSH). To fulfill this function optimally, the melanotrope cell undergoes plastic changes in structure and secretory activity in response to changed background light conditions. Xenopus melanotrope cells display Ca2+ oscillations that are thought to drive α-MSH secretion and gene expression. They also produce brain-derived neurotrophic factor (BDNF), which stimulates in an autocrine way the biosynthesis of the α-MSH precursor, pro-opiomelanocortin (POMC). We have used this physiological adaptation mechanism as a model to investigate the role of BDNF in the regulation of Ca2+ kinetics and Ca2+-dependent gene expression. By dynamic video imaging of isolated cultured melanotropes we demonstrated that BDNF caused a dose-dependent increase in Ca2+ oscillation frequency up to 64.7 ± 2.3% of control level. BDNF also induced a transient Ca2+ peak in Ca2+-free medium, which was absent when calcium stores were blocked by thapsigargin and 2-aminoethoxydiphenyl borate, indicating that BDNF stimulates acute release of Ca2+ from IP3-sensitive intracellular Ca2+ stores. Moreover, we show that thapsigargin inhibits the expression of BDNF transcript IV (by 61.1 ± 28.8%) but does not affect POMC transcript. We conclude that BDNF mobilizes Ca2+ from IP3-sensitive intracellular Ca2+ stores and propose the possibility that the resulting Ca2+ oscillations selectively stimulate expression of the BDNF gene.
Research highlights
► BDNF mobilizes Ca2+ from IP3-sensitive intracellular Ca2+ stores in Xenopus laevis melanotrope cell.
► Mobilization of intracellular Ca2+ leads to stimulated Ca2+ oscillations.
► Stimulated Ca2+ oscillation frequency may selectively stimulate expression of the BDNF gene.
Journal: General and Comparative Endocrinology - Volume 169, Issue 2, 1 November 2010, Pages 123–129