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抑制反应性神经胶质增生可防止氧诱导的视网膜病变小鼠模型中的新生血管生长。

Inhibition of reactive gliosis prevents neovascular growth in the mouse model of oxygen-induced retinopathy.

机构信息

Research Department, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.

出版信息

PLoS One. 2011;6(7):e22244. doi: 10.1371/journal.pone.0022244. Epub 2011 Jul 14.

Abstract

Retinal neovascularization (NV) is a major cause of blindness in ischemic retinopathies. Previous investigations have indicated that ischemia upregulates GFAP and PDGF-B expression. GFAP overexpression is a hallmark of reactive gliosis (RG), which is the major pathophysiological feature of retinal damage. In addition, PDGF-B has been implicated in proliferative retinopathies. It was the aim of this study to gain insights on the possible pharmacological interventions to modulate PDGF-B and GFAP expression, and its influence on RG and NV. We used an array of assays to evaluate the effects of YC-1, a small molecule inhibitor of HIF-1 and a novel NO-independent activator of soluble guanylyl cyclase (sGC), on RG and NV, in vivo and in vitro. When compared to the DMSO-treated retinas, dual-intravitreal injections of YC-1, in vivo: (1) suppressed the development and elongation of neovascular sprouts in the retinas of the oxygen-induced retinopathy (OIR) mouse model; and (2) reduced ischemia-induced overexpression of GFAP and PDGF-B at the message (by 64.14±0.5% and 70.27±0.04%) and the protein levels (by 65.52±0.02% and 57.59±0.01%), respectively. In addition, at 100 µM, YC-1 treatment downregulated the hypoxia-induced overexpression of GFAP and PDGF-B at the message level in rMC-1 cells (by 71.42±0.02% and 75±0.03%), and R28 cells (by 58.62±0.02% and 50.00±0.02%), respectively; whereas, the protein levels of GFAP and PDGF-B were reduced (by 78.57±0.02% and 77.55±0.01%) in rMC-1 cells, and (by 81.44±0.02% and 79.16±0.01%) in R28 cells, respectively. We demonstrate that YC-1 reversed RG during ischemic retinopathy via impairing the expression of GFAP and PDGF-B in glial cells. This is the first investigation that delves into the reversal of RG during ischemic retinal vasculopathies. In addition, the study reveals that YC-1 may exert promising therapeutic effects in the treatment of retinal and neuronal pathologies.

摘要

视网膜新生血管(NV)是缺血性视网膜病变致盲的主要原因。先前的研究表明,缺血会上调 GFAP 和 PDGF-B 的表达。GFAP 的过表达是反应性神经胶质增生(RG)的标志,这是视网膜损伤的主要病理生理特征。此外,PDGF-B 与增生性视网膜病变有关。本研究旨在深入了解可能的药物干预措施,以调节 PDGF-B 和 GFAP 的表达,并研究其对 RG 和 NV 的影响。我们使用一系列实验来评估小分子 HIF-1 抑制剂和新型 NO 非依赖性可溶性鸟苷酸环化酶(sGC)激活剂 YC-1 对体内和体外 RG 和 NV 的影响。与 DMSO 处理的视网膜相比,体内双重玻璃体内注射 YC-1:(1)抑制氧诱导的视网膜病变(OIR)小鼠模型中新生血管芽的发育和伸长;(2)减少缺血诱导的 GFAP 和 PDGF-B 的过度表达,mRNA 水平降低 64.14±0.5%和 70.27±0.04%,蛋白质水平降低 65.52±0.02%和 57.59±0.01%。此外,在 100µM 时,YC-1 处理可下调 rMC-1 细胞(mRNA 水平分别降低 71.42±0.02%和 75±0.03%)和 R28 细胞(mRNA 水平分别降低 58.62±0.02%和 50.00±0.02%)中缺氧诱导的 GFAP 和 PDGF-B 过度表达,而 rMC-1 细胞的 GFAP 和 PDGF-B 蛋白水平降低 78.57±0.02%和 77.55±0.01%,R28 细胞的 GFAP 和 PDGF-B 蛋白水平降低 81.44±0.02%和 79.16±0.01%。我们证明,YC-1 通过抑制神经胶质细胞中 GFAP 和 PDGF-B 的表达来逆转缺血性视网膜病变中的 RG。这是首次深入研究缺血性视网膜血管病变中 RG 的逆转。此外,该研究表明,YC-1 可能在治疗视网膜和神经元病变方面具有有前景的治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32d6/3136522/1733a2487040/pone.0022244.g001.jpg

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