体外
近曲小管
原代培养
病理
细胞培养
细胞生物学
化学
肾小管
表型
肾
肾切除术
生物
医学
内分泌学
生物化学
基因
遗传学
作者
Claire C. Sharpe,Mark E.C. Dockrell
出处
期刊:Methods in molecular biology
日期:2011-10-07
卷期号:: 175-185
被引量:20
标识
DOI:10.1007/978-1-61779-367-7_12
摘要
Renal physiology and pathology are complex systems that are best studied in whole living organisms. This, however, is often restricted by our desire to limit the number of animal experiments undertaken and to replace them with relevant in vitro models that can be used as surrogates for the system under test. Primary culture cells are derived directly from the relevant tissue and therefore correlate more closely with the system under examination. Although the tissue of origin is not always readily available for culture and cells may quickly change their phenotype after only a few passages, they can be used in many circumstances to validate results obtained from closely related cell lines and to confirm vital protein expression patterns. This chapter outlines methods by which proximal tubular epithelial cells and renal interstitial fibroblasts can be isolated and characterized from human renal nephrectomy tissue.
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