Sheridan Julie M, Visvader Jane E
Molecular Genetics of Cancer Division, Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, Australia.
Department of Medical Biology, University of Melbourne, Melbourne, VIC, Australia.
Methods Mol Biol. 2019;1940:217-229. doi: 10.1007/978-1-4939-9086-3_16.
Several methods of mammary gland dissociation have been described that utilize a combined strategy of mechanical and enzymatic dissociation to isolate mammary epithelial cells (MECs) from intact tissue (Smalley et al., J Mammary Gland Biol Neoplasia 17:91-97, 2012). Here we detail a robust method that enables the isolation of all major stem and progenitor MEC populations, which has been successfully used to study stem cell behavior when coupled with transplantation and in vitro assays (Shackleton et al., Nature 439:84-88, 2006; Bouras et al., Cell Stem Cell 3:429-441, 2008; Sheridan et al., BMC Cancer 15:221, 2015; Jamieson et al., Development 144:1065-1071, 2017). Furthermore, we outline two prominent methods for culturing MECs for the purposes of ex vivo manipulation or study: 2D feeder layer cultures and 3D Matrigel colony assays. Importantly, all outlined methods retain stem and progenitor cell behaviors and can be used in combination with downstream in vivo, in vitro, or in silico analyses.
已经描述了几种乳腺解离方法,这些方法采用机械和酶促解离相结合的策略,从完整组织中分离乳腺上皮细胞(MECs)(Smalley等人,《乳腺生物学与肿瘤学杂志》17:91 - 97,2012年)。在这里,我们详细介绍一种可靠的方法,该方法能够分离所有主要的干细胞和祖细胞MEC群体,当与移植和体外分析相结合时,已成功用于研究干细胞行为(Shackleton等人,《自然》439:84 - 88,2006年;Bouras等人,《细胞干细胞》3:429 - 441,2008年;Sheridan等人,《BMC癌症》15:221,2015年;Jamieson等人,《发育》144:1065 - 1071,2017年)。此外,我们概述了两种用于离体操作或研究目的培养MECs的主要方法:二维饲养层培养和三维基质胶集落分析。重要的是,所有概述的方法都保留了干细胞和祖细胞的行为,并且可以与下游的体内、体外或计算机分析相结合使用。