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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Upregulation of Myeloid Zinc Finger 1 in Dorsal Root Ganglion via Regulating Matrix Metalloproteinase-2/9 and Voltage-gated Potassium 1.2 Expression Contributes to Complete Freund's Adjuvant-induced Inflammatory Pain
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Upregulation of Myeloid Zinc Finger 1 in Dorsal Root Ganglion via Regulating Matrix Metalloproteinase-2/9 and Voltage-gated Potassium 1.2 Expression Contributes to Complete Freund's Adjuvant-induced Inflammatory Pain

机译:通过调节基质金属蛋白酶-2 / 9的背根神经节在背根神经节中上调,电压门控钾1.2表达有助于完全弗氏佐剂诱导的炎症疼痛

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摘要

Myeloid zinc finger 1 (MZF1) belongs to the Kruppel family of zinc-finger transcription factors. Recent studies have demonstrated that in dorsal root ganglion (DRG) neurons, MZF1 is involved in the development and maintenance of neuropathic pain. However, the role of MZF1 in inflammatory pain still remains unknown. In the present study, the mechanism of MZF1 in chronic inflammatory pain was investigated in rats received an intra-plantar injection of complete Freund's adjuvant (CFA). Subsequently, a series of assays including Western blotting, qRT-PCR, immunohistochemistry, and chromatin immunoprecipitation (ChIP) were performed. We found that CFA led to MZF1 upregulation in ipsilateral L4/5 DRGs. Pre- and post-microinjection of MZF1 siRNA into the ipsi-L5 DRG blocked the development of CFA-induced chronic inflammatory pain and alleviated the mechanical allodynia and thermal hyperalgesia in the maintenance phase. CFA also increased MMP-2/9 and Nav1.8 expression but reduced voltage-gated potassium 1.2 (Kv1.2) and Cav1.2 expression in L4/L5 DRGs. Microinjection of MZF1 siRNA into DRG diminished the CFA-induced changes in MMP-2/9 and Kv1.2 expression. However, the expressions of Nav1.8 and Cav1.2 were not changed by the treatment. Double immunofluorescence staining showed that MMP-2/9 and Kv1.2 were co-localized with MZF1 in DRGs. The ChIP-PCR results revealed that MZF1 binds directly to the promoter region of MMP-2/9 gene. Together, the above results imply that upregulation of MZF1 in DRGs might contribute to the development and maintenance of CFA-induced chronic inflammatory pain by regulating MMP-2/9 and Kv1.2 expression. Targeting DRG-localized MZF1 might be a promising therapeutic strategy for the treatment of chronic inflammatory pain in the clinic. (C) 2020 IBRO. Published by Elsevier Ltd. All rights reserved.
机译:髓锌手指1(MZF1)属于Kruppel系列的锌手指转录因子。最近的研究表明,在背根神经节(DRG)神经元中,MZF1参与了神经性疼痛的开发和维持。然而,MZF1在炎症疼痛中的作用仍然是未知的。在本研究中,在大鼠中研究了MZF1在慢性炎症疼痛中的机制接受了跖内注射完整的弗氏佐剂(CFA)。随后,进行了一系列测定,包括蛋白质印迹,QRT-PCR,免疫组织化学和染色质免疫沉淀(芯片)。我们发现CFA导致了IpsilateLal L4 / 5 DRG的MZF1上调。将MZF1 siRNA的微调和后显微注射进入IPSI-L5 DRG阻止了CFA诱导的慢性炎性疼痛的发育,并减轻了维持阶段的机械异常疼痛和热痛觉。 CFA还增加了MMP-2/9和NAV1.8表达,但在L4 / L5 DRG中减少了电压门控钾1.2(KV1.2)和CAV1.2表达。 MZF1 siRNA的显微注射到DRG减少了MMP-2/9和KV1.2表达的CFA诱导的变化。但是,NAV1.8和CAV1.2的表达没有通过治疗改变。双免疫荧光染色表明,MMP-2/9和KV1.2与DRG中的MZF1共局存。芯片PCR结果显示MZF1直接与MMP-2/9基因的启动子区结合。在一起,上述结果意味着通过调节MMP-2/9和KV1.2表达,DRG中MZF1的上调可能有助于CFA诱导的慢性炎性疼痛的开发和维持。靶向DRG局部化MZF1可能是治疗临床慢性炎症疼痛的有希望的治疗策略。 (c)2020年度IBRO。 elsevier有限公司出版。保留所有权利。

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