Shyu Woei-Cherng, Lin Shinn-Zong, Chiang Ming-Fu, Chen Der-Cherng, Su Ching-Yuan, Wang Hsiao-Jung, Liu Ren-Shyan, Tsai Chang-Hai, Li Hung
Center for Neuropsychiatry, China Medical University and Hospital, Taichung, Republic of China.
J Clin Invest. 2008 Jan;118(1):133-48. doi: 10.1172/JCI32723.
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.
促分泌素原神经肽(SN)是一种源自分泌粒蛋白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。在此,在大鼠中风模型和缺血性人脑组织中,SN在神经元和内皮细胞中均显著上调。SN介导的神经保护作用使原代皮质细胞培养物免受氧/葡萄糖剥夺。SN还通过Jak2/Stat3途径诱导抗凋亡蛋白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,脑梗死面积减小,运动功能改善,脑代谢活性增加。此外,SN注射增强了小鼠体内干细胞对损伤脑的靶向作用,并促进了新血管的形成,以增加缺血半球局部皮质血流。在体外和体内,SN不仅促进神经保护,还增强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途径促进其存活。