发布: 2017年12月20日第7卷第24期 DOI: 10.21769/BioProtoc.2659 浏览次数: 12871
评审: Liang-Chun WANGMahesh AppariAnonymous reviewer(s)
相关实验方案
来自骨髓增生性肿瘤患者的造血祖细胞的血小板生成素不依赖性巨核细胞分化
Chloe A. L. Thompson-Peach [...] Daniel Thomas
2023年01月20日 1312 阅读
Abstract
Direct isolation of human neural and glioma stem cells from fresh tissues permits their biological study without prior culture and may capture novel aspects of their molecular phenotype in their native state. Recently, we demonstrated the ability to prospectively isolate stem cell populations from fresh human germinal matrix and glioblastoma samples, exploiting the ability of cells to bind the Epidermal Growth Factor (EGF) ligand in fluorescence-activated cell sorting (FACS). We demonstrated that FACS-isolated EGF-bound neural and glioblastoma populations encompass the sphere-forming colonies in vitro, and are capable of both self-renewal and multilineage differentiation. Here we describe in detail the purification methodology of EGF-bound (i.e., EGFR+) human neural and glioma cells with stem cell properties from fresh postmortem and surgical tissues. The ability to prospectively isolate stem cell populations using native ligand-binding ability opens new doors for understanding both normal and tumor cell biology in uncultured conditions, and is applicable for various downstream molecular sequencing studies at both population and single-cell resolution.
Keywords: EGF (EGF)Background
Understanding the intrinsic biology of human neural and glioma stem cells has been challenging, due to the lack of universal neural and glioma stem cell markers (Lathia et al., 2015) and the frequent reliance on cultured cells rather than those isolated directly from the tissue. The transmembrane glycoprotein Prominin, or CD133, is one of the best described and frequently used stem cell markers for the isolation of neural (Uchida et al., 2000) and glioma stem cells (GSC) (Singh et al., 2003; Singh et al., 2004; Lathia et al., 2015), with its utility being demonstrated in both acutely sorted human tissues and neurospheres. However, some recent studies have pointed out that CD133-negative cells isolated from human glioblastoma (GBM) also harbor stem cell properties (Beier et al., 2007; Wang et al., 2008; Tome-Garcia et al., 2017). Other cell surface markers used to isolate GSC include CD44 (Anido et al., 2010), CD15 (Son et al., 2009), A2B5 (Ogden et al., 2008), integrin alpha (Lathia et al., 2010) or EGFR (Mazzoleni et al., 2010), but these antibody-based methodologies have also lacked the ability to capture all sphere-forming populations or their use has been limited to cultured cells.
A direct comparison of the molecular phenotypes between non-neoplastic and tumoral stem cell niches can provide novel insight into the developmental pathways co-opted during tumor formation and may uncover more comprehensive stem cell markers. In the context of gliomagenesis, several developmental pathways important for the growth and proliferation of normal neural progenitors have been demonstrated to be aberrantly reactivated during gliomagenesis (Sanai et al., 2005; Canoll and Goldman, 2008; Chen et al., 2012; Tsankova and Canoll, 2014; Lathia et al., 2015). Among these is the Epidermal Growth Factor Receptor (EGFR) tyrosine kinase pathway. Expression of EGFR is high during human neural development, especially within the germinal matrix stem cell niche, diminishing significantly in adulthood (Weickert et al., 2000; Sanai et al., 2011; Erfani et al., 2015), and it is aberrantly re-activated in GBM (Verhaak et al., 2010; Brennan et al., 2013). Recently, we adapted a mouse fluorescence-activated cell sorting (FACS) strategy, which selects for EGFR+ cells based on their native binding to EGF ligand (Ciccolini et al., 2005; Pastrana et al., 2009; Codega et al., 2014), and isolated human EGFR+ populations from fresh germinal matrix (GM) dissections and GBM tissues. This allowed us to directly compare the functional properties and whole-transcriptome signatures in developing and neoplastic neural populations (Tome-Garcia et al., 2017). EGFR+ populations from both GM and GBM tissues captured all sphere-forming cells in vitro, displayed similar proliferative stem cell properties, and shared transcriptome signatures related to cell growth and cell-cycle regulation. EGFR+ GBM populations also displayed tumor initiation in vivo (Tome-Garcia et al., 2017). Below, we describe this prospective purification strategy for neural and glioblastoma populations with stem cell properties from primary human samples, detailing the steps of tissue dissociation, ligand/antibody incubation, FACS, and in vitro functional stem cell property analysis.
Materials and Reagents
Equipment
Procedure
文章信息
版权信息
© 2017 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Tome-Garcia, J., Doetsch, F. and Tsankova, N. M. (2017). FACS-based Isolation of Neural and Glioma Stem Cell Populations from Fresh Human Tissues Utilizing EGF Ligand. Bio-protocol 7(24): e2659. DOI: 10.21769/BioProtoc.2659.
分类
癌症生物学 > 癌症干细胞 > 细胞生物学试验
干细胞 > 胚胎干细胞 > 基于细胞的分析方法
细胞生物学 > 细胞分离和培养 > 细胞分离
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