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原代培养大鼠中脑细胞上神经降压素结合位点的特性研究。

Characterization of neurotensin binding sites on rat mesencephalic cells in primary culture.

作者信息

Dana C, Pelaprat D, Vial M, Brouard A, Lhiaubet A M, Rostene W

机构信息

U. 339 INSERM, Hôpital Saint-Antoine, Paris France.

出版信息

Brain Res Dev Brain Res. 1991 Aug 19;61(2):259-64. doi: 10.1016/0165-3806(91)90139-a.

DOI:10.1016/0165-3806(91)90139-a
PMID:1661213
Abstract

Many studies have reported the presence of high amounts of neurotensin (NT) binding sites in the mesencephalon of adult rat, and their possible role in mediating the effects of the peptide on the activity of mesencephalic dopaminergic neurons. In the present study, we demonstrate the presence of NT sites in primary cultures of embryonic rat mesencephalic cells. On these cells, a single class of high affinity 125I-NT binding sites was observed. The value of the apparent affinity constant (0.3 nM) did not show any significant change throughout time, from 3 to 14 days in culture. The number of sites, however, increased until day 11 and decreased thereafter. Acetylneurotensin (8-13), NT and neuromedin N were potent competitors of 125I-NT binding, while NT (1-10), NT (1-11) and levocabastine were uneffective. These results indicate that the sites detected in the mesencephalic cultures share common binding properties with the high-affinity NT sites already described in adult rat brain. The neuronal localization of the NT sites was suggested by their presence in neuron-enriched serum-free cultures and their absence in glial cultures. Autoradiographic studies confirmed the cellular localization of NT sites and indicated that, under our experimental conditions, cells labeled by 125I-NT represented 0.14% of the initially plated cell number. Taken together, these results show that the development of mesencephalic neurons in primary culture is associated with an increased expression of NT binding sites. Since such cultures have been shown previously to contain functional dopaminergic neurons, we suggest that they could provide a good model to investigate the modulation of the activity of these neurons by NT.

摘要

许多研究报告称,成年大鼠中脑存在大量神经降压素(NT)结合位点,及其在介导该肽对中脑多巴胺能神经元活性影响方面的可能作用。在本研究中,我们证明了胚胎大鼠中脑细胞原代培养物中存在NT位点。在这些细胞上,观察到一类单一的高亲和力125I-NT结合位点。在培养3至14天的整个时间段内,表观亲和常数的值(0.3 nM)未显示出任何显著变化。然而,位点数量在第11天之前增加,之后减少。乙酰神经降压素(8-13)、NT和神经介素N是125I-NT结合的有效竞争者,而NT(1-10)、NT(1-11)和左卡巴斯汀则无效。这些结果表明,在中脑培养物中检测到的位点与成年大鼠脑中已描述的高亲和力NT位点具有共同的结合特性。NT位点的神经元定位是由其在富含神经元的无血清培养物中的存在以及在胶质细胞培养物中的缺失所提示的。放射自显影研究证实了NT位点的细胞定位,并表明在我们的实验条件下,被125I-NT标记的细胞占最初接种细胞数的0.14%。综上所述,这些结果表明原代培养的中脑神经元的发育与NT结合位点表达的增加有关。由于此前已证明此类培养物含有功能性多巴胺能神经元,我们认为它们可以提供一个良好的模型来研究NT对这些神经元活性的调节作用。

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