前沿| Peptain-1可阻断缺血/再灌注诱导的小鼠视网膜毛细血管变性

IF 4.2 3区 医学 Q2 NEUROSCIENCES Frontiers in Cellular Neuroscience Pub Date : 2024-07-16 DOI:10.3389/fncel.2024.1441924
Mi-Hyun Nam, Armaan Dhillon, Rooban B. Nahomi, Noelle L. Carrillo, Clarinda S. Hougen, Ram H. Nagaraj
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引用次数: 0

摘要

导言神经血管变性会导致血管功能障碍、渗漏、缺血和结构变化,从而导致严重的视力损伤。我们以前曾在两种青光眼动物模型中发现过eptain-1对视网膜神经节细胞的保护作用,eptain-1是一种来自αB-结晶素核心结构域的20个氨基酸肽。在此,我们评估了eptain-1在体外阻断人视网膜内皮细胞(HRECs)凋亡的能力,以及在视网膜缺血/再灌注(I/R)损伤小鼠体内阻断视网膜毛细血管变性的能力。方法用eptain-1或加扰肽(200 μg/mL)处理HRECs 3小时,再用促炎细胞因子组合(IFN-γ 20 ng/mL + TNF-α 20 ng/mL+ IL-1β 20 ng/mL)处理48小时。将 C57BL/6J 小鼠(12 周大)的眼内压升高至 120 mmHg,使其受到 I/R 损伤 60 分钟,然后进行再灌注。在 I/R 损伤后立即和 7 天后静脉注射 Peptain-1 或加扰肽(0.5 μg)。动物在 I/R 损伤后第 14 天安乐死。结果我们的数据显示,培达-1能进入HRECs并阻止促炎细胞因子介导的细胞凋亡。玻璃体内给药的 peptain-1 在 4 小时后分布于整个视网膜血管。I/R 损伤导致视网膜毛细血管变性。与干扰肽不同,培达-1能保护毛细血管免受I/R损伤。讨论我们的研究表明,培达-1可作为一种治疗剂,用于预防视网膜缺血时的毛细血管变性和神经炎症。
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Frontiers | Peptain-1 blocks ischemia/reperfusion-induced retinal capillary degeneration in mice
IntroductionNeurovascular degeneration results in vascular dysfunction, leakage, ischemia, and structural changes that can lead to significant visual impairment. We previously showed the protective effects of peptain-1, a 20 amino acid peptide derived from the αB-crystallin core domain, on retinal ganglion cells in two animal models of glaucoma. Here, we evaluated the ability of peptain-1 to block apoptosis of human retinal endothelial cells (HRECs) in vitro and retinal capillary degeneration in mice subjected to retinal ischemia/reperfusion (I/R) injury.MethodsHRECs were treated with either peptain-1 or scrambled peptides (200 μg/mL) for 3 h and a combination of proinflammatory cytokines (IFN-γ 20 ng/mL + TNF-α 20 ng/mL+ IL-1β 20 ng/mL) for additional 48 h. Apoptosis was measured with cleaved caspase-3 formation via western blot, and by TUNEL assay. C57BL/6J mice (12 weeks old) were subjected to I/R injury by elevating the intraocular pressure to 120 mmHg for 60 min, followed by reperfusion. Peptain-1 or scrambled peptide (0.5 μg) was intravitreally injected immediately after I/R injury and 7 days later. One microliter of PBS was injected as vehicle control, and animals were euthanized on day 14 post-I/R injury. Retinal capillary degeneration was assessed after enzyme digestion followed by periodic acid–Schiff staining.ResultsOur data showed that peptain-1 entered HRECs and blocked proinflammatory cytokine-mediated apoptosis. Intravitreally administered peptain-1 was distributed throughout the retinal vessels after 4 h. I/R injury caused retinal capillary degeneration. Unlike scrambled peptide, peptain-1 protected capillaries against I/R injury. Additionally, peptain-1 inhibited microglial activation and reduced proinflammatory cytokine levels in the retina following I/R injury.DiscussionOur study suggests that peptain-1 could be used as a therapeutic agent to prevent capillary degeneration and neuroinflammation in retinal ischemia.
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来源期刊
CiteScore
7.90
自引率
3.80%
发文量
627
审稿时长
6-12 weeks
期刊介绍: Frontiers in Cellular Neuroscience is a leading journal in its field, publishing rigorously peer-reviewed research that advances our understanding of the cellular mechanisms underlying cell function in the nervous system across all species. Specialty Chief Editors Egidio D‘Angelo at the University of Pavia and Christian Hansel at the University of Chicago are supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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