Immortalization of mouse primary astrocytes

星形胶质细胞 永生化细胞系 生物 端粒酶逆转录酶 细胞培养 端粒酶 SV40大T抗原 抗原 神经胶质 细胞生物学 U87型 胶质纤维酸性蛋白 电池类型 小胶质细胞 细胞 免疫学 中枢神经系统 神经科学 转染 遗传学 炎症 免疫组织化学 基因
作者
Weihong Yi,Dazhi Yang,Zhen Xu,Zecai Chen,Guozhi Xiao,Lei Qin
出处
期刊:Gene [Elsevier]
卷期号:865: 147327-147327 被引量:4
标识
DOI:10.1016/j.gene.2023.147327
摘要

In cell culture studies, immortalized primary cells have become a useful tool to investigate the molecular and cellular functions of different types of cells. Several immortalization agents, such as human telomerase reverse transcriptase (hTERT) and Simian Virus 40 (SV40) T antigens, are commonly used for primary cell immortalization. Astrocytes, as the most abundant glial cell type in the central nervous system, are promising therapeutical targets for many neuronal disorders, such as Alzheimer’s disease and Parkinson’s disease. Immortalized primary astrocytes can provide useful information for astrocytes biology, astrocytes-neuron interactions, glial interactions and astrocytes-associated neuronal diseases. In this study, we successfully purified primary astrocytes with immuno-panning method and examined the astrocyte functions after immortalization through both hTERT and SV40 Large-T antigens. As expected, both immortalized astrocytes presented unlimited lifespan and highly expressed multiple astrocyte-specific markers. However, SV40 Large-T antigen, but not hTERT, immortalized astrocytes displayed fast ATP-induced calcium wave in culture. Hence, SV40 Large-T antigen could be a better choice for primary astrocyte immortalization, which closely mimics the cell biology of primary astrocytes in culture. In summary, the purification and immortalization of primary astrocytes presented in this study can be used for studying astrocyte biology under physiological and pathological conditions.
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