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Bcl-2/E1B-19KD-相互作用蛋白 3/轻链 3 相互作用在体内和体外诱导大鼠脊髓损伤中的自噬。

Bcl-2/E1B-19KD-Interacting Protein 3/Light Chain 3 Interaction Induces Mitophagy in Spinal Cord Injury in Rats Both In Vivo and In Vitro.

机构信息

1 Department of Orthopedics, Xinqiao Hospital, Third Military Medical University , Chongqing, China .

2 Department of Cardiothoracic Surgery, PLA 421 Hospital , Guangzhou, China .

出版信息

J Neurotrauma. 2018 Sep 15;35(18):2183-2194. doi: 10.1089/neu.2017.5280. Epub 2018 Jun 7.

Abstract

Autophagy and mitophagy have been shown to occur in spinal cord injury (SCI). Bcl-2/E1B-19KD-interacting protein 3 (BNIP3) and its homologue, NIX, have been implicated in the regulation of mitophagy. The aim of this work was to characterize the mechanisms and role of BNIP3 in SCI-associated mitophagy. Our data showed that BNIP3, targeted to mitochondria, interacted with microtubule-associated protein 1A/1B-light chain 3 (LC3), which is targeted to autophagosomes, thus forming a mitochondria-BNIP3-LC3-autophagosome complex and resulting in mitophagy. Downregulation of BNIP3 by RNA interference strengthened the mitochondrial function and decreased cell death in spinal cord neurons under hypoxia. Particularly, BNIP3 knockdown significantly improved neurological recovery and the number of neuronal nuclei-positive cells post-SCI in rats. The present study demonstrated that BNIP3 interacts with LC3 to induce mitophagy, whereas its inhibition provided protective neuronal effects in SCI rat models both in vivo and in vitro.

摘要

自噬和线粒体自噬已被证明存在于脊髓损伤(SCI)中。Bcl-2/E1B-19KD 相互作用蛋白 3(BNIP3)及其同源物 NIX 已被牵连到线粒体自噬的调节中。本研究旨在描述 BNIP3 在 SCI 相关线粒体自噬中的作用机制。我们的数据表明,靶向线粒体的 BNIP3 与微管相关蛋白 1A/1B-轻链 3(LC3)相互作用,LC3 靶向自噬体,从而形成线粒体-BNIP3-LC3-自噬体复合物,并导致线粒体自噬。通过 RNA 干扰下调 BNIP3 可增强缺氧条件下脊髓神经元的线粒体功能并减少细胞死亡。特别是,BNIP3 敲低显著改善了 SCI 大鼠的神经功能恢复和神经元核阳性细胞数量。本研究表明 BNIP3 与 LC3 相互作用诱导线粒体自噬,而抑制 BNIP3 可在体内和体外 SCI 大鼠模型中提供保护神经元的作用。

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