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垂体细胞中电压门控性Ca2+通道的表达以及缺水期间L型Ca2+通道的上调。

The expression of voltage-gated ca2+ channels in pituicytes and the up-regulation of L-type ca2+ channels during water deprivation.

作者信息

Wang D, Yan B, Rajapaksha W R A K J S, Fisher T E

机构信息

Department of Physiology, College of Medicine, University of Saskatchewan, Saskatoon, SK, Canada.

出版信息

J Neuroendocrinol. 2009 Oct;21(10):858-66. doi: 10.1111/j.1365-2826.2009.01906.x. Epub 2009 Aug 4.

Abstract

The primary components of the neurohypophysis are the neuroendocrine terminals that release vasopressin and oxytocin, and pituicytes, which are astrocytes that normally surround and envelop these terminals. Pituicytes regulate neurohormone release by secreting the inhibitory modulator taurine in an osmotically-regulated fashion and undergo a marked structural reorganisation in response to dehydration as well as during lactation and parturition. Because of these unique functions, and the possibility that Ca2+ influx could regulate their activity, we tested for the expression of voltage-gated Ca2+ channel alpha1 subunits in pituicytes both in situ and in primary culture. Colocalisation studies in neurohypophysial slices show that pituicytes (identified by their expression of the glial marker S100beta), are immunoreactive for antibodies directed against Ca2+ channel alpha1 subunits Ca(V)2.2 and Ca(V)2.3, which mediate N- and R-type Ca2+ currents, respectively. Pituicytes in primary culture express immunoreactivity for Ca(V)1.2, Ca(V)2.1, Ca(V)2.2, Ca(V)2.3 and Ca(V)3.1 (which mediate L-, P/Q-, N-, R- and T-type currents, respectively) and immunoblotting studies confirmed the expression of these Ca2+ channel alpha1 subunits. This increase in Ca2+ channel expression may occur only in pituicytes in culture, or may reflect an inherent capability of pituicytes to initiate the expression of multiple types of Ca2+ channels when stimulated to do so. We therefore performed immunohistochemistry studies on pituitaries obtained from rats that had been deprived of water for 24 h. Pituicytes in these preparations showed a significantly increased immunoreactivity to Ca(V)1.2, suggesting that expression of these channels is up-regulated during the adaptation to long-lasting dehydration. Our results suggest that Ca2+ channels may play important roles in pituicyte function, including a contribution to the adaptation that occurs in pituicytes when the need for hormone release is elevated.

摘要

神经垂体的主要组成部分是释放血管加压素和催产素的神经内分泌终末,以及垂体细胞,垂体细胞是通常围绕并包裹这些终末的星形胶质细胞。垂体细胞通过以渗透压调节的方式分泌抑制性调节剂牛磺酸来调节神经激素的释放,并在脱水以及哺乳和分娩期间经历明显的结构重组。由于这些独特的功能,以及Ca2+内流可能调节其活性的可能性,我们在原位和原代培养中检测了垂体细胞中电压门控Ca2+通道α1亚基的表达。神经垂体切片的共定位研究表明,垂体细胞(通过其胶质标志物S100β的表达来鉴定)对分别介导N型和R型Ca2+电流的针对Ca2+通道α1亚基Ca(V)2.2和Ca(V)2.3的抗体具有免疫反应性。原代培养中的垂体细胞对Ca(V)1.2、Ca(V)2.1、Ca(V)2.2、Ca(V)2.3和Ca(V)3.1(分别介导L型、P/Q型、N型、R型和T型电流)具有免疫反应性,免疫印迹研究证实了这些Ca2+通道α1亚基的表达。Ca2+通道表达的这种增加可能仅发生在培养的垂体细胞中,或者可能反映了垂体细胞在受到刺激时启动多种类型Ca2+通道表达的内在能力。因此,我们对从缺水24小时的大鼠获得的垂体进行了免疫组织化学研究。这些制剂中的垂体细胞对Ca(V)1.2的免疫反应性显著增加,表明在适应长期脱水过程中这些通道的表达上调。我们的结果表明,Ca2+通道可能在垂体细胞功能中发挥重要作用,包括在激素释放需求增加时垂体细胞发生的适应性变化中起作用。

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