Article ID Journal Published Year Pages File Type
2801820 General and Comparative Endocrinology 2008 9 Pages PDF
Abstract
We have tested the hypothesis that the type and kinetics of voltage-activated Ca2+ channels in a neuroendocrine cell depend on the cell's long-term external input. For this purpose, the presence and kinetics of both low (LVA) and high-voltage-activated (HVA) L-type Ca2+ channels have been assessed in melanotrope pituitary cells of the amphibian Xenopus laevis. The secretory activity of this cell type can readily be manipulated in vivo by changing the animal's environmental light condition, from a black to a white background. We here show that, compared to white background-adapted Xenopus, melanotropes from black background-adapted frogs have (1) a much larger size, as revealed by their 2.5 times larger membrane capacitance (P < 0.001), (2) a 2 times higher HVA current density (P < 0.05), (3) a clearly smaller Ca2+-dependent inactivation (10%; P < 0.05), (4) L-type channels with 5 times slower activation and inactivation kinetics (P < 0.05), and (5) slower kinetics of L-type channels that become faster and more similar to those in white-background adapted cells when the intracellular Ca2+-buffering capacity is reduced. Furthermore, white-adapted melanotropes possess LVA-type Ca2+ channels, which are lacking from cells from black-adapted animals. The melanotrope calmodulin mRNA level does not differ between the two adaptation states. These results indicate that HVA L-type channel kinetics differ in relation to environmentally induced changes in cellular secretory state, probably mediated via intracellular Ca2+-buffering, whereas the occurrence of LVA Ca2+ channels may depend on environmentally controlled channel gene expression.
Related Topics
Life Sciences Biochemistry, Genetics and Molecular Biology Endocrinology
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