State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yet-Sen University, Guangzhou 510060, China.
State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yet-Sen University, Guangzhou 510060, China.
Cell Immunol. 2018 Jun;328:49-57. doi: 10.1016/j.cellimm.2018.03.006. Epub 2018 Mar 16.
This study was conducted to investigate the use of Alpha 1-antitrypsin (AAT) to inhibit microglia activation in chronic hypertension model and provide a permissive environment for stem cell transplantation. Chronic ocular hypertension of C57BL/6 mice using magnetic microbead injection was induced 3 weeks prior to iPSCs transplantation. The ocular hypertension model was assessed histologically and intraocular pressure was measured. Survival of grafted cells and microglia activation were examined by flow cytometry and immunofluorescence in AAT and PBS treated hosts. Retinal cytokines expression was also detected by real-time PCR. Chronic ocular hypertension resulted in persistent microglia activation and stem cell grafts loss. AAT treatment significantly inhibited microglia activation and facilitated the survival of transplant iPSCs 4w post transplantation compared to PBS treatment. AAT holds tremendous potential for the clinical application to control neuroinflammation factor in glaucoma and improve the stem cell replacement therapy of retinal neurodegenerative disease.
本研究旨在探讨使用 Alpha 1-抗胰蛋白酶 (AAT) 抑制慢性高血压模型中的小胶质细胞活化,为干细胞移植提供许可环境。在 iPSCs 移植前 3 周,使用磁性微珠注射诱导 C57BL/6 小鼠慢性眼内压升高。通过组织学评估和眼内压测量来评估眼内高压模型。通过流式细胞术和 AAT 和 PBS 处理宿主中的免疫荧光检查移植细胞和小胶质细胞活化的存活情况。通过实时 PCR 检测视网膜细胞因子的表达。慢性眼内高压导致持续的小胶质细胞活化和干细胞移植物丢失。与 PBS 处理相比,AAT 处理在移植后 4 周显著抑制小胶质细胞活化并促进移植 iPSCs 的存活。AAT 在控制青光眼神经炎症因子和改善视网膜神经退行性疾病的干细胞替代治疗方面具有巨大的临床应用潜力。