Knock-down of POSH expression is neuroprotective through down-regulating activation of the MLK3–MKK4–JNK pathway following cerebral ischaemia in the rat hippocampal CA1 subfield

Authors

  • Quan-Guang Zhang,

    1. Department of Neurobiology and Biophysics, University of Science and Technology of China, Hefei, Anhui, China
    2. Research Center for Biochemistry and Molecular Biology, Xuzhou Medical College, Xuzhou, China
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  • Rui-Min Wang,

    1. Research Center for Biochemistry and Molecular Biology, Xuzhou Medical College, Xuzhou, China
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  • Xiao-Hui Yin,

    1. Research Center for Biochemistry and Molecular Biology, Xuzhou Medical College, Xuzhou, China
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  • Jing Pan,

    1. Research Center for Biochemistry and Molecular Biology, Xuzhou Medical College, Xuzhou, China
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  • Tian-Le Xu,

    1. Department of Neurobiology and Biophysics, University of Science and Technology of China, Hefei, Anhui, China
    2. Institute of Neuroscience, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China
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  • Guang-Yi Zhang

    1. Department of Neurobiology and Biophysics, University of Science and Technology of China, Hefei, Anhui, China
    2. Research Center for Biochemistry and Molecular Biology, Xuzhou Medical College, Xuzhou, China
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Address correspondence and reprint requests to Guang-Yi Zhang, Research Center for Biochemistry and Molecular Biology, Xuzhou Medical College, 84 West Huai-hai Road, Xuzhou, Jiangsu 221002, China. E-mail: gyzhang@xzmc.edu.cn

Abstract

We investigated the expression and subcellular localization of the multidomain protein POSH (plenty of SH3s) by immunohistochemistry and western blot analysis, as well as its role in the selective activation of mixed-lineage kinases (MLKs) 3, MAP kinase kinase (MKK) 4, c-Jun N-terminal kinases (JNKs) and the c-Jun signalling cascade in the rat hippocampal CA1 region following cerebral ischaemia. Our results indicated that the cytosol immunoreactivity of POSH was strong in the CA1-CA3 pyramidal cell but weak in the DG granule cell of the rat hippocampus both in sham control and after reperfusion. Co-immunoprecipitation experiments showed that the interactions of MLK3, MKK4 and phospho-JNKs with POSH were persistently enhanced during the early (30 min) and the later reperfusion period (from 1 to 3 days) compared with sham controls. Consistently, MLK3–MKK4–JNK activation was rapidly increased with peaks both at 30 min and 3 days of reperfusion. Intracerebroventricular infusion of POSH antisense oligodeoxynucleotides (AS-ODNs) not only significantly reduced the protein level of POSH, markedly decreased its interactions with MLK3, MKK4 and phospho-JNKs, but also attenuated the activation of the JNK signalling pathway. In addition, infusion of POSH AS-ODNs significantly increased the neuronal density in the CA1 region at 5 days of reperfusion. Our results suggest that POSH might serve as a scaffold mediating JNK signalling activation in the hippocampal CA1 region following cerebral ischaemia, and POSH AS-ODNs exerts its protective effects on ischaemic injury through a mechanism of inhibition of the MLK3–MKK4–JNK signalling pathway, involving c-Jun and caspase 3 activation.

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