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DOI: 10.3791/64244-v
Feng Wen*1,2,3, Yanzi Wang*1,2,3, Danxue He1,2,3, Chunyan Liao1,2,3, Weijie Ouyang1,2,3, Zuguo Liu1,2,3, Wei Li1,2,3, Yi Liao1,2,3
1Eye Institute of Xiamen University, Fujian Provincial Key Laboratory of Ophthalmology and Visual Science, School of Medicine,Xiamen University, 2Department of Ophthalmology, Xiang'an Hospital of Xiamen University, School of Medicine,Xiamen University, 3Xiamen University Affiliated Xiamen Eye Center, School of Medicine,Xiamen University
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This study presents a straightforward protocol for culturing primary porcine retinal pigment epithelial (RPE) cells in vitro, addressing the challenges associated with RPE-related disorders. The method aims to create a reliable model for studying the physiological and pathological aspects of these disorders, facilitating new treatment development.
本文介绍了一种易于遵循的体 外 培养原代猪视网膜色素上皮细胞的方法。
RPE相关疾病仍然是混合疾病的主要部分,但在原代RPE细胞的虚拟培养中没有有效的残留物,无法作为RPE相关疾病的生理和病理学研究的良好模型。在该协议中,我们提供了一种易于遵循的实验方案来培养初级IPC,可以快速恢复和维持以后的RP特征,我们相信通过使用这种方法,人们可以从无痕状态研究和保护性药物筛选中快速产生RP细胞,这可以促进RPE疾病的新治疗方法的开发。分步价值演示将使该方法更容易在想要研究RP细胞的不同实验室中复制。
开始解冻组织消化酶马拉夸德并灭菌1X PBS。通过0.22微米注射器过滤装置过滤溶液,补充2%青霉素和2%链霉素。用1X PBS清洗培养板和跨孔插入物的孔。
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