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首页> 外文期刊>Biochemical and Biophysical Research Communications >CART peptide promotes the survival of hippocampal neurons by upregulating brain-derived neurotrophic factor.
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CART peptide promotes the survival of hippocampal neurons by upregulating brain-derived neurotrophic factor.

机译:CART肽通过上调脑源性神经营养因子来促进海马神经元的存活。

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摘要

The neuropeptide cocaine- and amphetamine-regulated transcript (CARTp) plays a role in various physiological processes. CARTp is highly expressed in rat hippocampus and can promote the survival and differentiation of neurons in primary hippocampal cell cultures. However, little is known about the neurotrophic mechanism of CARTp on the hippocampal neuron. We show that CARTp fragment 55-102 promoted the survival of cultured hippocampal neurons by increasing the number of surviving neurons and their viability. The tyrosine kinase B (TrkB) antibody, known to inhibit the activity of brain-derived neurotrophic factor (BDNF), blocked the survival-promoting effect of CARTp on hippocampal neurons. Further study by reverse-transcription PCR showed that BDNF mRNA expression significantly increased after CARTp treatment. The prepro BDNF and mature BDNF protein also increased in level as seen on Western blot analysis. Thus, the neurotrophic effects of CARTp on cultured hippocampal neurons are mediated through the upregulation of BDNF mRNA expression and protein synthesis. The results of the present study suggest the therapeutic efficacy of CARTp in neurodegenerative disorders.
机译:神经肽可卡因和苯丙胺调节的转录本(CARTp)在各种生理过程中发挥作用。 CARTp在大鼠海马中高表达,可以促进原代海马细胞培养物中神经元的存活和分化。然而,关于CARTp对海马神经元的神经营养机制知之甚少。我们显示,CARTp片段55-102通过增加存活神经元的数量及其生存能力来促进培养的海马神经元的存活。已知抑制脑源性神经营养因子(BDNF)活性的酪氨酸激酶B(TrkB)抗体阻断了CARTp对海马神经元的存活促进作用。通过逆转录PCR的进一步研究表明,在CARTp处理后,BDNF mRNA表达显着增加。如蛋白质印迹分析所示,prepro BDNF和成熟的BDNF蛋白的水平也增加了。因此,CARTp对培养的海马神经元的神经营养作用是通过上调BDNF mRNA表达和蛋白质合成来介导的。本研究的结果提示了CARTp在神经退行性疾病中的治疗功效。

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