首页> 外文期刊>The Journal of Clinical Investigation: The Official Journal of the American Society for Clinical Investigation >Secretoneurin promotes neuroprotection and neuronal plasticity via the Jak2/Stat3 pathway in murine models of stroke.
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Secretoneurin promotes neuroprotection and neuronal plasticity via the Jak2/Stat3 pathway in murine models of stroke.

机译:Secretoneurin 通过卒中小鼠模型中的 Jak2/Stat3 通路促进神经保护和神经元可塑性。

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摘要

Secretoneurin (SN), a neuropeptide derived from secretogranin II, promotes neurite outgrowth of immature cerebellar granule cells. SN also aids in the growth and repair of neuronal tissue, although the precise mechanisms underlying the promotion of brain tissue neuroprotection and plasticity by SN are not understood. Here, in a rat model of stroke and in ischemic human brain tissue, SN was markedly upregulated in both neurons and endothelial cells. SN-mediated neuroprotection rescued primary cortical cell cultures from oxygen/glucose deprivation. SN also induced expression of the antiapoptotic proteins Bcl-2 and Bcl-xL through the Jak2/Stat3 pathway and inhibited apoptosis by blocking caspase-3 activation. In addition, rats with occluded right middle cerebral arteries showed less cerebral infarction, improved motor performance, and increased brain metabolic activity following i.v. administration of SN. Furthermore, SN injection enhanced stem cell targeting to the injured brain in mice and promoted the formation of new blood vessels to increase local cortical blood flow in the ischemic hemisphere. Both in vitro and in vivo, SN not only promoted neuroprotection, but also enhanced neurogenesis and angiogenesis. Our results demonstrate that SN acts directly on neurons after hypoxia and ischemic insult to further their survival by activating the Jak2/Stat3 pathway.
机译:分泌素 (SN) 是一种来源于分泌颗粒蛋白 II 的神经肽,可促进未成熟小脑颗粒细胞的神经突生长。SN 还有助于神经元组织的生长和修复,尽管 SN 促进脑组织神经保护和可塑性的确切机制尚不清楚。在这里,在中风的大鼠模型和缺血性人脑组织中,SN在神经元和内皮细胞中显着上调。SN 介导的神经保护将原代皮质细胞培养物从氧气/葡萄糖剥夺中拯救出来。SN 还通过 Jak2/Stat3 通路诱导抗凋亡蛋白 Bcl-2 和 Bcl-xL 的表达,并通过阻断 caspase-3 激活来抑制细胞凋亡。此外,右大脑中动脉闭塞的大鼠在静脉注射SN后表现出较少的脑梗死,运动性能改善和脑代谢活动增加。此外,SN注射增强了干细胞对小鼠受伤大脑的靶向性,并促进了新血管的形成,以增加缺血半球的局部皮质血流量。无论是在体外还是在体内,SN不仅促进了神经保护,还增强了神经发生和血管生成。我们的结果表明,SN在缺氧和缺血性损伤后直接作用于神经元,通过激活Jak2/Stat3通路来促进其存活。

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