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大鼠脑海绵状室周器官区域来源的培养细胞中血管加压素受体的特性分析。

Characterization of vasopressin receptors in cultured cells derived from the region of rat brain circumventricular organs.

作者信息

Jurzak M, Müller A R, Gerstberger R

机构信息

Max-Planck-Institut für physiologische und klinische Forschung, W. G. Kerckhoff-Institut, Bad Nauheim, Germany.

出版信息

Neuroscience. 1995 Apr;65(4):1145-59. doi: 10.1016/0306-4522(94)00539-h.

Abstract

The aim of the present study was to characterize vasopressin receptors within the two circumventricular organs located in the lamina terminalis of the rat brain, namely the organum vasculosum of the lamina terminalis and the subfornical organ. Cells derived from both structures were isolated, cultured and intracellular Ca2+ concentrations were measured in single fura-2 loaded neurons and astrocytes after application of vasopressin and various vasopressin analogues. Subsequent to Ca2+ measurements, the identification of neurons and astrocytes was verified using immunocytochemistry with cell type-specific antibodies. High proportions of subfornical organ (34%) and organum vasculosum laminae terminalis (28%) neurons exhibited increased intracellular Ca2+ concentration after exposure to 1-1000 nM vasopressin. Within single cells, the response was dose-dependent. Similar results were obtained in subfornical organ (62%) and organum vasculosum laminae terminalis (38%) astrocytes with minor differences in the transient amplitude and pattern distribution when compared with neurons. Since omission of extracellular Ca2+ preserved vasopressin responsiveness, it is likely that intracellular stores were the main source of mobilized Ca2+. The preincubation of neurons and astrocytes with the V1 receptor-specific antagonist d(CH2)5[Tyr(Me)2]8-arginine vasopressin (10-100 nM) selectively and reversibly blocked the vasopressin-mediated response. Oxytocin-induced Ca2+ transients (0.32-1000 nM), which were observed in 32% (63%) or organum vasculosum laminae terminalis and in 54% (42%) of subfornical organ neurons (astrocytes), were not affected by the V1-specific antagonist. These data indicate the presence of a V1-like vasopressin receptor and an oxytocin receptor in cultured neurons and astrocytes from both circumventricular organ structures. In addition, the exposure to the highly selective V2 receptor agonist, 1-desamino,8-D-arginine vasopressin, evoked Ca2+ transients almost exclusively in organum vasculosum laminae terminalis neurons (eight of 18 tested). Only 1 (n = 14) subfornical organ neuron and none of the astrocytes tested (n = 26) responded to 1-desamino,8-D-arginine vasopressin. Since 1-desamino,8-D-arginine vasopressin acting via "classical" V2 receptors is not expected to affect the intracellular Ca2+ concentration, these data indicate the tissue and cell type-specific expression of a 1-desamino,8-D-arginine vasopressin-sensitive vasopressin receptor in neurons of the organum vasculosum laminae terminalis. In summary, the results indicate a heterogeneity of neurohypophyseal peptide receptor subtypes in the primary cell culture of both circumventricular structures.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

本研究的目的是对大鼠脑终板内两个室周器官(即终板血管器和穹窿下器官)中的血管加压素受体进行表征。从这两个结构中分离出细胞,进行培养,并在应用血管加压素和各种血管加压素类似物后,测量单个负载fura - 2的神经元和星形胶质细胞内的Ca2 +浓度。在进行Ca2 +测量之后,使用细胞类型特异性抗体通过免疫细胞化学法验证神经元和星形胶质细胞的身份。暴露于1 - 1000 nM血管加压素后,高比例的穹窿下器官(34%)和终板血管器(28%)神经元表现出细胞内Ca2 +浓度升高。在单个细胞内,反应呈剂量依赖性。在穹窿下器官(62%)和终板血管器(38%)星形胶质细胞中也获得了类似结果,与神经元相比,瞬时振幅和模式分布存在细微差异。由于省略细胞外Ca2 +可保留血管加压素反应性,因此细胞内储存可能是Ca2 +动员的主要来源。用V1受体特异性拮抗剂d(CH2)5[Tyr(Me)2]8 - 精氨酸血管加压素(10 - 100 nM)对神经元和星形胶质细胞进行预孵育,可选择性且可逆地阻断血管加压素介导的反应。在32%(终板血管器为63%)的终板血管器和54%(穹窿下器官为42%)的穹窿下器官神经元(星形胶质细胞)中观察到的催产素诱导的Ca2 +瞬变(0.32 - 1000 nM)不受V1特异性拮抗剂影响。这些数据表明在来自这两个室周器官结构的培养神经元和星形胶质细胞中存在类似V1的血管加压素受体和催产素受体。此外,暴露于高度选择性的V2受体激动剂1 - 去氨基,8 - D - 精氨酸血管加压素后,几乎仅在终板血管器神经元(18个测试中有8个)中诱发Ca2 +瞬变。仅1个(n = 14)穹窿下器官神经元和测试的星形胶质细胞中无一(n = 26)对1 - 去氨基,8 - D - 精氨酸血管加压素有反应。由于通过“经典”V2受体起作用的1 - 去氨基,8 - D - 精氨酸血管加压素预计不会影响细胞内Ca2 +浓度,这些数据表明在终板血管器神经元中存在对1 - 去氨基,8 - D - 精氨酸血管加压素敏感的血管加压素受体的组织和细胞类型特异性表达。总之,结果表明在这两个室周结构的原代细胞培养中神经垂体肽受体亚型存在异质性。(摘要截断于400字)

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