...
首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Dopamine D3 receptor stimulation promotes the proliferation of cells derived from the post-natal subventricular zone.
【24h】

Dopamine D3 receptor stimulation promotes the proliferation of cells derived from the post-natal subventricular zone.

机译:多巴胺D3受体刺激可促进源自出生后脑室下区的细胞增殖。

获取原文
获取原文并翻译 | 示例

摘要

In the adult mammalian brain, neural stem cells persist in the subventricular zone (SVZ) where dopamine D3 receptors are expressed. Here, we demonstrate that addition of 1 microm apomorphine increases cell numbers in post-natal SVZ cell cultures. This effect was prevented by a co-treatment with haloperidol, sulpiride or U-99194A, a D3-preferring antagonist, and mimicked by the dopamine D3 receptor selective agonist 7-hydroxy-dipropylaminotetralin (7-OH-DPAT). EC50 values were 4.04 +/- 1.54 nm for apomorphine and 0.63 +/- 0.13 nm for 7-OH-DPAT, which fits the pharmacological profile of the D3 receptor. D3 receptors were detected in SVZ cells by RT-PCR and immunocytochemistry. D3 receptors were expressed in numerous beta-III tubulin immunopositive cells. The fraction of apoptotic nuclei remained unchanged following apomorphine treatment, thus ruling out any possible effect on cell survival. In contrast, proliferation was increased as both the proportion of nuclei incorporating bromo-deoxyuridine and the expression of the cell division marker cyclin D1 were enhanced. These findings provide support for a regulatory role of dopamine over cellular dynamics in post-natal SVZ.
机译:在成年哺乳动物的大脑中,神经干细胞在多巴胺D3受体表达的脑室下区域(SVZ)中持续存在。在这里,我们证明了添加1微米的阿扑吗啡会增加出生后SVZ细胞培养物中的细胞数量。通过与氟哌啶醇,舒必利或U-99194A(一种D3优先的拮抗剂)共同治疗可防止此作用,并由多巴胺D3受体选择性激动剂7-羟基-二丙基氨基四氢萘(7-OH-DPAT)模拟。阿扑吗啡的EC50值为4.04 +/- 1.54 nm,7-OH-DPAT的EC50值为0.63 +/- 0.13 nm,这与D3受体的药理特性相吻合。通过RT-PCR和免疫细胞化学在SVZ细胞中检测到D3受体。 D3受体在众多的β-III微管蛋白免疫阳性细胞中表达。阿朴吗啡处理后,凋亡核的分数保持不变,因此排除了对细胞存活的任何可能影响。相反,随着掺入溴脱氧尿苷的核比例和细胞分裂标志物cyclin D1的表达均增加,增殖增加。这些发现为多巴胺对产后SVZ中细胞动力学的调节作用提供了支持。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号