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SRC 抑制的 C 激酶底物在大鼠星形胶质细胞慢性缩窄损伤后的关键作用。

A critical role of SRC-suppressed C kinase substrate in rat astrocytes after chronic constriction injury.

机构信息

Department of Microbiology and Immunology, Medical College, Nantong University, Nantong, Jiangsu, China.

出版信息

Neuromolecular Med. 2010 Sep;12(3):205-16. doi: 10.1007/s12017-009-8093-y. Epub 2009 Nov 25.

Abstract

Src-suppressed C kinase substrate (SSeCKS), is an in vivo and in vitro protein kinase C substrate that may have a role in both mitogenic regulation and cytoskeletal arrangement. In this study, we mainly investigated the mRNA and protein expression and cellular localization of SSeCKS during chronic constriction injury (CCI). Reverse transcriptase-mediated PCR and western blot analysis revealed that SSeCKS was present in normal whole spinal cord. It gradually increased, and reached a peak at 2 weeks for its mRNA level and 7 days for its protein level after CCI. The protein expression of SSeCKS was further analyzed by immunohistochemistry. The positively stained areas for SSeCKS changed with the similar pattern to that of protein expression detected by immunoblotting analysis. Double immunofluorescence staining showed SSeCKS immunoreactivity was mostly co-localized with neurons, partly with activated astrocytes and rarely with microglia in the superficial laminar of spinal dorsal horn. In cell culture, the expression of pro-inflammation cytokines, p-ERK, and SSeCKS was increased in the spinal astrocytes after stimulated by damaged sensory neurons. However, SSeCKS gene silencing by siRNA inhibited the up-regulation of p-ERK and the pro-inflammation cytokines. Taken together, activated astrocytes released cytokines and iNOS after neuropathic pain via SSeCKS-ERK signaling. SSeCKS might be critical for the activation of astrocytes in the neuropathic pain.

摘要

Src 抑制型蛋白激酶底物(SSeCKS)是一种体内和体外蛋白激酶 C 的底物,可能在有丝分裂调节和细胞骨架排列中起作用。在这项研究中,我们主要研究了慢性压迫损伤(CCI)过程中 SSeCKS 的 mRNA 和蛋白表达及其细胞定位。逆转录介导的 PCR 和 Western blot 分析显示 SSeCKS 存在于正常的全脊髓中。它逐渐增加,在 CCI 后 2 周达到 mRNA 水平的峰值,7 天达到蛋白水平的峰值。通过免疫组织化学进一步分析 SSeCKS 的蛋白表达。SSeCKS 的阳性染色区域与免疫印迹分析检测到的蛋白表达的相似模式发生变化。双重免疫荧光染色显示 SSeCKS 免疫反应性主要与神经元共定位,部分与激活的星形胶质细胞共定位,与小胶质细胞很少共定位。在细胞培养中,损伤感觉神经元刺激后,脊髓星形胶质细胞中促炎细胞因子、p-ERK 和 SSeCKS 的表达增加。然而,siRNA 沉默 SSeCKS 基因抑制了 p-ERK 和促炎细胞因子的上调。总之,神经病理性疼痛通过 SSeCKS-ERK 信号转导,激活的星形胶质细胞释放细胞因子和 iNOS。SSeCKS 可能对神经病理性疼痛中星形胶质细胞的激活至关重要。

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