Department of Anesthesiology, And College of Medicine, University of Illinois at Chicago, Chicago, IL, USA.
Department of Chemistry, College of Liberal Arts and Sciences, University of Illinois at Chicago, Chicago, IL, USA.
Autophagy. 2021 Jun;17(6):1479-1499. doi: 10.1080/15548627.2020.1767371. Epub 2020 May 26.
Retinal ischemia is a major cause of vision loss and a common underlying mechanism associated with diseases, such as diabetic retinopathy and central retinal artery occlusion. We have previously demonstrated the robust neuroprotection in retina induced by post-conditioning (post-C), a brief period of ischemia, 24 h, following a prolonged and damaging initial ischemia. The mechanisms underlying post-C-mediated retinal protection are largely uncharacterized. We hypothesized that macroautophagy/autophagy is a mediator of post-C-induced neuroprotection. This study employed an model of oxygen glucose deprivation (OGD) in the retinal R28 neuronal cell line, and an rat model of retinal ischemic injury. , there were significant increases in autophagy proteins, MAP1LC3-II/LC3-II, and decreases in SQSTM1/p62 (sequestosome 1) in ischemia/post-C . ischemia/sham post-C. Blockade of and decreased LC3-II, increased SQSTM1, attenuated the functional protective effect of post-C, and increased histological damage and TUNEL compared to non-silencing siRNA. TUNEL after ischemia was found in retinal ganglion, amacrine, and photoreceptor cells. Blockade of attenuated the post-C neuroprotection by a brief period of OGD . Moreover, , post-C attenuated cell death, loss of cellular proliferation, and defective autophagic flux from prolonged OGD. Stimulating autophagy using Tat-Beclin 1 rescued retinal neurons from cell death after OGD. As a whole, our results suggest that autophagy is required for the neuroprotective effect of retinal ischemic post-conditioning and augmentation of autophagy offers promise in the treatment of retinal ischemic injury.: BECN1: Beclin 1, autophagy related; DAPI: 4',6-diamidino-2-phenylindole; DR: diabetic retinopathy; EdU: 5-ethynyl-2'-deoxyuridine; ERG: Electroretinogram; FITC: Fluorescein isothiocyanate; GCL: Ganglion cell layer; GFAP: Glial fibrillary acidic protein; INL: Inner nuclear layer; IPL: Inner plexiform layer; MAP1LC3/LC3: Microtubule-associated protein 1 light chain 3; OGD: Oxygen-glucose deprivation; ONL: Outer nuclear layer; OP: Oscillatory potential; PFA: Paraformaldehyde; PL: Photoreceptor layer; post-C: post-conditioning; RFP: Red fluorescent protein; RGC: Retinal ganglion cell; RPE: Retinal pigment epithelium; RT-PCR: Real-time polymerase chain reaction; SEM: Standard error of the mean; siRNA: Small interfering RNA; SQSTM1: Sequestosome 1; STR: Scotopic threshold response; Tat: Trans-activator of transcription; TUNEL: Terminal deoxynucleotidyl transferase dUTP nick end labeling.
视网膜缺血是视力丧失的主要原因,也是与糖尿病视网膜病变和中央视网膜动脉阻塞等疾病相关的常见潜在机制。我们之前已经证明了后处理(post-C)在诱导视网膜中强大的神经保护作用,即短暂的缺血期,在长时间和损伤性初始缺血后 24 小时。后处理介导的视网膜保护的机制在很大程度上尚未确定。我们假设巨自噬/自噬是 post-C 诱导的神经保护的介质。本研究采用视网膜 R28 神经元细胞系的氧葡萄糖剥夺(OGD)模型和大鼠视网膜缺血性损伤模型。结果发现,在缺血/后-C 中,自噬蛋白 MAP1LC3-II/LC3-II 显著增加,而 SQSTM1/p62(自噬体 1)减少。与假缺血/后-C 相比,缺血/Sham 后-C 中的自噬标志物 LC3-II 减少,而 SQSTM1 增加。与非沉默 siRNA 相比,后-C 的功能保护作用减弱,组织学损伤和 TUNEL 增加。在视网膜神经节细胞、无长突细胞和光感受器细胞中发现了 TUNEL 后缺血。Beclin 1 的短暂 OGD 抑制了后-C 的神经保护作用。此外,后-C 减轻了长期 OGD 引起的细胞死亡、细胞增殖丧失和缺陷自噬流。用 Tat-Beclin 1 刺激自噬可挽救 OGD 后视网膜神经元的死亡。总的来说,我们的结果表明自噬是视网膜缺血后处理的神经保护作用所必需的,并且增强自噬为治疗视网膜缺血性损伤提供了希望。