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Secretoneurin promotes neuroprotection and neuronal plasticity via the Jak2/Stat3 pathway in murine models of stroke
Woei-Cherng Shyu, … , Chang-Hai Tsai, Hung Li
Woei-Cherng Shyu, … , Chang-Hai Tsai, Hung Li
Published December 13, 2007
Citation Information: J Clin Invest. 2008;118(1):133-148. https://doi.org/10.1172/JCI32723.
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Research Article Cardiology

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

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Abstract

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.

Authors

Woei-Cherng Shyu, Shinn-Zong Lin, Ming-Fu Chiang, Der-Cherng Chen, Ching-Yuan Su, Hsiao-Jung Wang, Ren-Shyan Liu, Chang-Hai Tsai, Hung Li

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Figure 1

Cerebral ischemia increases expression of SN in human and rat brain.

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Cerebral ischemia increases expression of SN in human and rat brain.
(A)...
(A) Representative brain of a stroke patient; boxed region shows infarct area. IHC studies of the penumbral area showed markedly increased SN-IR. (B) SN-IR in the stroke patients’ brains significantly increased at 1 and 3 days after cerebral infarction compared with that of controls. (C and D) IHC and quantitative analysis of SN-IR of animal cerebral ischemia (boxed region) showed greater numbers of SN-IR cells compared with controls. (E and F) Measurement of SN level using ELISA at the indicated time points showed a significant increase of SN expression in both ischemic rats’ brains and stroke patients’ sera compared with controls. (G) Double immunofluorescence with laser-scanning confocal microscopy of ischemic rat brain specimens. The ischemic cortical areas of the rats revealed SN-IR cells coexpressing Neu-N+. Some SN-IR cells showing vascular phenotypes (SMA+ cells) were also found around the perivascular and endothelial regions of the ischemic hemispheres. Data are mean ± SEM. *P < 0.05, **P < 0.01 vs. control. Scale bars: 50 μm.

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