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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Differential signaling of glial cell line-derived neurothrophic factor and brain-derived neurotrophic factor in cultured ventral mesencephalic neurons.
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Differential signaling of glial cell line-derived neurothrophic factor and brain-derived neurotrophic factor in cultured ventral mesencephalic neurons.

机译:腹侧中脑神经元中胶质细胞源性神经营养因子和脑源性神经营养因子的差异信号传递。

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摘要

In the ventral mesencephalon, two neurotrophic factors, brain-derived neurotrophic factor and glial cell line-derived neurotrophic factor, have been shown previously to have similar effects on the survival of dopaminergic neurons. Here, we compared the signaling mechanisms for brain-derived neurotrophic factor and glial cell line-derived neurotrophic factor, focusing on the mitogen-associated protein kinase and the transcription factor cyclic-AMP responsive element-binding protein. Double-staining experiments indicated that many neurons co-expressed the receptors for glial cell line-derived neurotrophic factor and brain-derived neurotrophic factor, c-RET and TrkB, suggesting that they are responsive to both brain-derived neurotrophic factor and glial cell line-derived neurotrophic factor. Although both brain-derived neurotrophic factor and glial cell line-derived neurotrophic factor induced a rapid phosphorylation of mitogen-associated protein kinase and cyclic-AMP, responsive element-binding protein, there were significant differences in the kinetics and pharmacology of the phosphorylation. The phosphorylation of mitogen-associated protein kinase by glial cell line-derived neurotrophic factor was transient; within 2 h, the level of mitogen-associated protein kinase phosphorylation returned to baseline. In contrast, the effect of brain-derived neurotrophic factor was long lasting; the mitogen-associated protein kinase remained phosphorylated for up to 4 h after brain-derived neurotrophic factor treatment. PD098059, a specific inhibitor for mitogen-associated protein kinase kinase, completely blocked the glial cell line-derived neurotrophic factor signaling through mitogen-associated protein kinase, but had no effect on brain-derived neurotrophic factor-induced mitogen-associated protein kinase phosphorylation. Both brain-derived neurotrophic factor and glial cell line-derived neurotrophic factor induced the phosphorylation of cyclic-AMP responsive element-binding protein in the nuclei of ventral mesencephalon neurons. However, PD098059 blocked the cyclic-AMP responsive element-binding protein phosphorylation induced by glial cell line-derived neurotrophic factor, but not that by brain-derived neurotrophic factor. These results indicate that, although both brain-derived neurotrophic factor and glial cell line-derived neurotrophic factor act on ventral mesencephalon neurons, the two factors have different signaling mechanisms, which may mediate their distinctive biological functions.
机译:在腹侧中脑中,先前已显示出两种神经营养因子,即脑源性神经营养因子和神经胶质细胞系源性神经营养因子,对多巴胺能神经元的存活具有相似的作用。在这里,我们比较了脑源性神经营养因子和神经胶质细胞系源性神经营养因子的信号传导机制,重点研究了促分裂原相关蛋白激酶和转录因子环状AMP响应元件结合蛋白。双重染色实验表明,许多神经元共表达神经胶质细胞源性神经营养因子和脑源性神经营养因子,c-RET和TrkB的受体,这表明它们对脑源性神经营养因子和神经胶质细胞系均具有响应衍生的神经营养因子。尽管脑源性神经营养因子和神经胶质细胞系源性神经营养因子均诱导了促分裂原相关蛋白激酶和环状AMP,响应元件结合蛋白的快速磷酸化,但是在磷酸化的动力学和药理学方面存在显着差异。胶质细胞源性神经营养因子使丝裂原相关蛋白激酶的磷酸化是瞬时的。在2小时内,与丝裂原相关的蛋白激酶磷酸化水平恢复到基线。相反,脑源性神经营养因子的作用持久。在脑源性神经营养因子治疗后,有丝分裂原相关蛋白激酶保持磷酸化长达4小时。 PD098059是一种与促细胞分裂素相关的蛋白激酶激酶的特异性抑制剂,它通过促细胞分裂剂相关的蛋白激酶完全阻断了神经胶质细胞系的神经营养因子信号转导,但对脑源性神经营养因子诱导的促细胞分裂素相关的蛋白激酶磷酸化没有影响。脑源性神经营养因子和神经胶质细胞系源性神经营养因子均诱导腹侧中脑神经元细胞核中AMP响应元件结合蛋白的磷酸化。然而,PD098059阻断了由神经胶质细胞系衍生的神经营养因子诱导的环-AMP响应元件结合蛋白的磷酸化,但没有阻断脑衍生的神经营养因子所诱导的。这些结果表明,尽管脑源性神经营养因子和胶质细胞系源性神经营养因子都作用于腹侧中脑神经元,但这两种因子具有不同的信号传导机制,可能介导其独特的生物学功能。

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