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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Brain-derived neurotrophic factor causes cAMP response element-binding protein phosphorylation in absence of calcium increases in slices and cultured neurons from rat visual cortex.
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Brain-derived neurotrophic factor causes cAMP response element-binding protein phosphorylation in absence of calcium increases in slices and cultured neurons from rat visual cortex.

机译:脑源性神经营养因子导致cAMP反应元件结合蛋白的磷酸化,而切片和培养的大鼠视皮层神经元中的钙却没有增加。

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摘要

Neurotrophins play a crucial role in the developmental plasticity of the visual cortex, but very little is known about the cellular mechanisms involved in their action. In many models of synaptic plasticity, increases in cytosolic calcium concentration and activation of the transcription factor cAMP response element-binding protein (CREB) are crucial factors for the induction and maintenance of long-lasting changes of synaptic efficacy. Whether BDNF modulates intracellular calcium levels in visual cortical neurons and the significance of this action for BDNF signal transduction is still controversial. We investigated whether CREB phosphorylation and calcium changes are elicited by acute BDNF presentation in postnatal visual cortical slices and cultures. We found that BDNF did not cause any calcium increase, but it induced robust CREB phosphorylation in neurons from both preparations. We further analyzed signal transduction and its dependency on calcium changes in cultured neurons. CREB phosphorylation required trkB activation because treatment with the trk inhibitor k252a completely blocked CREB phosphorylation. In agreement with the imaging experiments, we verified that calcium changes were not necessary for CREB activation because preincubation with BAPTA-AM did not diminish the level of CREB phosphorylation induced by BDNF stimulation. CREB phosphorylation was accompanied by gene expression, because we observed the upregulation of c-fos expression, which was also not affected by preincubation with BAPTA-AM. Finally, BDNF caused phosphorylation of mitogen-activated protein kinase (MAPK), and because the treatment with the MAPK inhibitor U0126 completely abolished CREB activation and c-fos upregulation, it is likely that both processes depend mainly on the MAP kinase pathway. These results indicate that MAPK and CREB, but not intracellular calcium, are important mediators of neurotrophin actions in the visual cortex.
机译:神经营养蛋白在视觉皮层的发育可塑性中起着至关重要的作用,但对其作用所涉及的细胞机制知之甚少。在许多突触可塑性模型中,胞浆钙浓度的增加和转录因子cAMP反应元件结合蛋白(CREB)的激活是诱导和维持突触功效长期变化的关键因素。 BDNF是否调节视觉皮层神经元中的细胞内钙水平以及该作用对BDNF信号转导的意义仍存在争议。我们调查了CREB磷酸化和钙的变化是否由出生后视觉皮层切片和培养物中的急性BDNF表现引起。我们发现BDNF不会引起任何钙的增加,但会在两种制剂的神经元中引起强烈的CREB磷酸化。我们进一步分析了信号转导及其对培养的神经元中钙变化的依赖性。 CREB磷酸化需要trkB激活,因为用trk抑制剂k252a处理完全阻断了CREB磷酸化。与成像实验一致,我们证实钙的改变对于CREB激活不是必需的,因为与BAPTA-AM一起预孵育不会降低BDNF刺激引起的CREB磷酸化水平。 CREB磷酸化伴随基因表达,因为我们观察到c-fos表达的上调,这也不受BAPTA-AM预温育的影响。最后,BDNF导致丝裂原激活的蛋白激酶(MAPK)磷酸化,并且由于用MAPK抑制剂U0126进行的治疗完全消除了CREB激活和c-fos上调,因此这两个过程都可能主要取决于MAP激酶途径。这些结果表明,MAPK和CREB,而不是细胞内钙,是视觉皮层中神经营养蛋白作用的重要介体。

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