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血管内皮生长因子A(VEGFA)和血管生成素2(ANGPT2)抗体对链脲佐菌素诱导的糖尿病视网膜病变发病早期小胶质细胞激活的影响

Effects of VEGFA and ANGPT2 Antibodies on the Activation of Microglia in the Early Stages of Streptozotocin-Induced Pathogenesis of Diabetic Retinopathy.

作者信息

Iwagawa Toshiro, Inokuchi Yuta, Saita Kosuke, Soeda Tetsuhiro, Usui-Ouchi Ayumi, Aihara Makoto, Watanabe Sumiko

机构信息

Department of Retinal Biology and Pathology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.

Product Research Department, Chugai Pharmaceutical Co., Ltd., Tokyo, Japan.

出版信息

Genes Cells. 2025 Jul;30(4):e70036. doi: 10.1111/gtc.70036.

Abstract

Diabetic retinopathy (DR) is known as a microvascular complication, in which various inflammatory symptoms, including activation of microglia, are observed. A model of hyperglycemia resembling type 1 diabetes mellitus (DM) induced in mice by intraperitoneal injection of streptozotocin (STZ) has been widely used. We examined the effects of anti- vascular endothelial growth factor A (VEGFA) and anti-angiopoietin-2 (ANGPT2) antibodies in addition to a bispecific antibody against VEGFA and ANGPT2 by intravitreously administrated to the eyes on early signs, especially the activation of microglia in STZ-treated mice eyes. After 14 weeks of STZ administration, alterations in activity by ERG and CD31 staining patterns were not observed. Although a difference in the number of microglia in the retina between normal and STZ-model retinas was not observed, the morphology of microglia had changed from ramified in control to amoeboid shape in STZ model at 4 days after the antibodies injection. Detailed morphological examination showed decreases in area, ramification index, and tree length in the STZ-model retinas compared with normal retinas. Recovery from these decreases was demonstrated mainly by the administration of the bispecific antibody. These results suggest that anti-VEGFA/ANGPT2 therapy may suppress the activation of microglia in the early stages of DR.

摘要

糖尿病视网膜病变(DR)是一种微血管并发症,在其中可观察到包括小胶质细胞激活在内的各种炎症症状。通过腹腔注射链脲佐菌素(STZ)在小鼠中诱导出的类似1型糖尿病(DM)的高血糖模型已被广泛使用。我们通过向眼睛玻璃体内注射抗血管内皮生长因子A(VEGFA)和抗血管生成素-2(ANGPT2)抗体以及一种针对VEGFA和ANGPT2的双特异性抗体,来研究其对早期症状的影响,特别是对STZ处理的小鼠眼睛中小胶质细胞激活的影响。在给予STZ 14周后,未观察到视网膜电图(ERG)活动和CD31染色模式的改变。虽然在正常视网膜和STZ模型视网膜之间未观察到视网膜中小胶质细胞数量的差异,但在注射抗体4天后,小胶质细胞的形态已从对照中的分支状变为STZ模型中的阿米巴样形状。详细的形态学检查显示,与正常视网膜相比,STZ模型视网膜的面积、分支指数和树突长度均减少。主要通过给予双特异性抗体证明了这些减少的恢复。这些结果表明,抗VEGFA/ANGPT2疗法可能在DR的早期阶段抑制小胶质细胞的激活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a260/12187618/8b321dbefcfc/GTC-30-0-g001.jpg

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