Suppr超能文献

大鼠坐骨神经慢性压迫损伤后,脊髓背角中核STAT2蛋白的下调与神经性疼痛有关。

Downregulation of nuclear STAT2 protein in the spinal dorsal horn is involved in neuropathic pain following chronic constriction injury of the rat sciatic nerve.

作者信息

Huang Zhifeng, Ding Zijing, Xu Yangting, Xi Caiyun, He Liqiong, Luo Hui, Guo Qulian, Huang Changsheng

机构信息

Department of Anesthesiology, Xiangya Hospital, Central South University, Changsha, China.

Xiangya School of Medicine, Central South University, Changsha, China.

出版信息

Front Pharmacol. 2023 Jan 18;14:1069331. doi: 10.3389/fphar.2023.1069331. eCollection 2023.

Abstract

Regulation of gene transcription in the spinal dorsal horn (SDH) plays a critical role in the pathophysiology of neuropathic pain. In this study, we investigated whether the transcription factor STAT2 affects neuropathic pain and evaluated its possible mechanisms. A proteomic analysis showed that the nuclear fraction of STAT2 protein in the SDH was downregulated after chronic constriction injury of the rat sciatic nerve, which was associated with the development of neuropathic pain. Similarly, siRNA-induced downregulation of STAT2 in the SDH of naïve rats also resulted in pain hypersensitivity. Using RNA-sequencing analysis, we showed that reduction of nuclear STAT2 after chronic constriction injury was associated with increased expression of microglial activation markers, including the class II transactivator and major histocompatibility complex class II proteins. In addition, siRNA-induced downregulation of STAT2 promoted microglial activation and pro-inflammatory cytokine expression in the SDH. Taken together, these results showed that chronic constriction injury caused downregulation of nuclear STAT2 in the SDH, which may result in microglial activation and development of neuropathic pain. Our findings indicate that restoration of nuclear expression of STAT2 could be a potential pathway for the treatment of neuropathic pain.

摘要

脊髓背角(SDH)中的基因转录调控在神经性疼痛的病理生理学中起着关键作用。在本研究中,我们调查了转录因子信号转导和转录激活因子2(STAT2)是否影响神经性疼痛,并评估了其可能的机制。蛋白质组学分析表明,大鼠坐骨神经慢性压迫损伤后,SDH中STAT2蛋白的核部分下调,这与神经性疼痛的发展有关。同样,在未处理的大鼠SDH中,小干扰RNA(siRNA)诱导的STAT2下调也导致疼痛超敏反应。通过RNA测序分析,我们发现慢性压迫损伤后核STAT2的减少与小胶质细胞激活标志物的表达增加有关,包括II类反式激活因子和主要组织相容性复合体II类蛋白。此外,siRNA诱导的STAT2下调促进了SDH中小胶质细胞的激活和促炎细胞因子的表达。综上所述,这些结果表明慢性压迫损伤导致SDH中核STAT2下调,这可能导致小胶质细胞激活和神经性疼痛的发展。我们的研究结果表明,恢复STAT2的核表达可能是治疗神经性疼痛的潜在途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b63c/9890072/0d0291219443/fphar-14-1069331-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验