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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >MELATONIN ENHANCES ADULT RAT HIPPOCAMPAL PROGENITOR CELL PROLIFERATION VIA ERK SIGNALING PATHWAY THROUGH MELATONIN RECEPTOR
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MELATONIN ENHANCES ADULT RAT HIPPOCAMPAL PROGENITOR CELL PROLIFERATION VIA ERK SIGNALING PATHWAY THROUGH MELATONIN RECEPTOR

机译:褪黑素通过褪黑素受体通过ERK信号通路增强成年大鼠海马祖细胞的增殖

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Melatonin, a neurohormone secreted mainly by the pineal gland, has a variety of physiological functions and neuroprotective effects. Previous studies have shown that melatonin could stimulate the proliferation of neural stem/progenitor cells (NS/PCs). Recent studies reported that the activities of mitogen-activated protein kinase (MAPK) of neural stem cells (NSCs) changed in response to the prolif-erative effect of melatonin. Therefore, the aim of the present study was to explore the proliferative mechanism mediated by melatonin on the adult rat hippocampal NS/PCs. Treatment with melatonin significantly increased the number of neurospheres in a concentration-dependent manner and up-regulated nestin protein. Pretreatment with luzindole, a melatonin receptor antagonist, and PD98059, a mitogen-activated protein kinase kinase (MEK) inhibitor, prevented the increase in the number of neurospheres formed by the activation of melatonin. The levels of phospho-c-Raf and phospho-extracellular signal-regulated kinase 1/2 (ERK1/2) increased when treated with melatonin. Pretreatment with luzindole or PD98059 prevented the melatonin-induced increase in these signaling molecules. The present results showed that melatonin could induce NS/PCs to proliferate by increasing phosphorylation of ERK1/2 and c-Raf through melatonin receptor. These results provide further evidence for a role of melatonin in promoting neurogenesis, adding to the remarkably pleiotropic nature of this neurohormone. This intrinsic modulator deserves further investigation to better understand its physiological and therapeutic implication.
机译:褪黑激素是一种主要由松果体分泌的神经激素,具有多种生理功能和神经保护作用。先前的研究表明,褪黑激素可以刺激神经干/祖细胞(NS / PCs)的增殖。最近的研究报道,神经干细胞(NSCs)的促分裂原活化蛋白激酶(MAPK)的活性响应于褪黑激素的增生作用而改变。因此,本研究的目的是探讨褪黑激素介导的对成年大鼠海马NS / PCs的增殖机制。褪黑素治疗以浓度依赖性方式显着增加神经球的数量,并上调巢蛋白。用褪黑激素受体拮抗剂luzindole和有丝分裂原激活的蛋白激酶激酶(MEK)抑制剂PD98059进行预处理,可以防止因褪黑激素激活而形成的神经球数量增加。褪黑素处理后,磷酸化c-Raf和磷酸化细胞外信号调节激酶1/2(ERK1 / 2)的水平增加。用luzindole或PD98059预处理可防止褪黑激素诱导的这些信号分子增加。目前的结果表明,褪黑激素可以通过增加褪黑激素受体引起的ERK1 / 2和c-Raf的磷酸化来诱导NS / PCs增殖。这些结果为褪黑素在促进神经发生中的作用提供了进一步的证据,从而增加了这种神经激素的显着多效性。这种内在调节剂值得进一步研究,以更好地了解其生理和治疗意义。

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