Secretoneurin promotes neuroprotection and neuronal plasticity via the Jak2/Stat3 pathway in murine models of stroke

被引:134
|
作者
Shyu, Woei-Cherng [1 ]
Lin, Shinn-Zong [1 ]
Chiang, Ming-Fu [2 ]
Chen, Der-Cherng [3 ]
Su, Ching-Yuan [4 ]
Wang, Hsiao-Jung [1 ]
Liu, Ren-Shyan [5 ]
Tsai, Chang-Hai [6 ]
Li, Hung [4 ]
机构
[1] China Med Univ & Hosp, Ctr Neuropsychiat, Taichung 40447, Taiwan
[2] Mackay Jr Coll Nursing, Mackay Mem Hosp, Dept Neurosurg, Taipei, Taiwan
[3] Tzu Chi Univ, Buddhist Tzu Chi Gen Hosp, Dept Neurosurg, Hualien, Peoples R China
[4] Acad Sinica, Inst Mol Biol, Taipei 115, Taiwan
[5] Natl Yang Ming Univ, Taipei Vet Gen Hosp, Dept Nucl Med, Taipei 112, Taiwan
[6] China Med Univ & Hosp, Dept Pediat, Taichung, Taiwan
来源
JOURNAL OF CLINICAL INVESTIGATION | 2008年 / 118卷 / 01期
关键词
D O I
10.1172/JCI32723
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
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.
引用
收藏
页码:133 / 148
页数:16
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