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二甲双胍通过抑制中性粒细胞浸润和 MMP-9 表达,而不是直接调节 TJ 蛋白表达,来改善血脑屏障破坏。

Metformin ameliorates BSCB disruption by inhibiting neutrophil infiltration and MMP-9 expression but not direct TJ proteins expression regulation.

机构信息

Department of Orthopaedics, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang Province, China.

Zhejiang Provincial Key Laboratory of Orthopaedics, Wenzhou, Zhejiang Province, China.

出版信息

J Cell Mol Med. 2017 Dec;21(12):3322-3336. doi: 10.1111/jcmm.13235. Epub 2017 Jul 12.

Abstract

Blood-spinal cord barrier (BSCB) disruption is a major process for the secondary injury of spinal cord injury (SCI) and is considered to be a therapeutic target for SCI. Previously, we demonstrated that metformin could improve functional recovery after SCI; however, the effect of metformin on BSCB is still unknown. In this study, we found that metformin could prevent the loss of tight junction (TJ) proteins at day 3 after SCI in vivo, but in vitro there was no significant difference of these proteins between control and metformin treatment in endothelial cells. This indicated that metformin-induced BSCB protection might not be mediated by up-regulating TJ proteins directly, but by inhibiting TJ proteins degradation. Thus, we investigated the role of metformin on MMP-9 and neutrophils infiltration. Neutrophils infiltration is the major source of the enhanced MMP-9 in SCI. Our results showed that metformin decreased MMP-9 production and blocked neutrophils infiltration at day 1 after injury, which might be related to ICAM-1 down-regulation. Also, our in vitro study showed that metformin inhibited TNF-α-induced MMP-9 up-regulation in neutrophils, which might be mediated via an AMPK-dependent pathway. Together, it illustrated that metformin prevented the breakdown of BSCB by inhibiting neutrophils infiltration and MMP-9 production, but not by up-regulating TJ proteins expression. Our study may help to better understand the working mechanism of metformin on SCI.

摘要

血-脊髓屏障(BSCB)破坏是脊髓损伤(SCI)继发性损伤的主要过程,被认为是 SCI 的治疗靶点。先前,我们证明了二甲双胍可以改善 SCI 后的功能恢复;然而,二甲双胍对 BSCB 的影响尚不清楚。在这项研究中,我们发现二甲双胍可以防止 SCI 后第 3 天体内紧密连接(TJ)蛋白的丢失,但在体外,内皮细胞中 TJ 蛋白在对照组和二甲双胍治疗组之间没有显著差异。这表明,二甲双胍诱导的 BSCB 保护可能不是通过直接上调 TJ 蛋白来介导的,而是通过抑制 TJ 蛋白的降解来介导的。因此,我们研究了二甲双胍对 MMP-9 和中性粒细胞浸润的作用。中性粒细胞浸润是 SCI 中增强 MMP-9 的主要来源。我们的结果表明,二甲双胍在损伤后第 1 天减少了 MMP-9 的产生并阻止了中性粒细胞的浸润,这可能与 ICAM-1 的下调有关。此外,我们的体外研究表明,二甲双胍抑制了 TNF-α诱导的中性粒细胞中 MMP-9 的上调,这可能是通过 AMPK 依赖途径介导的。综上所述,二甲双胍通过抑制中性粒细胞浸润和 MMP-9 的产生来防止 BSCB 的破坏,而不是通过上调 TJ 蛋白的表达来实现。我们的研究可能有助于更好地理解二甲双胍对 SCI 的作用机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e5b/5706495/7ca3cdda648d/JCMM-21-3322-g001.jpg

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