发布: 2017年08月05日第7卷第15期 DOI: 10.21769/BioProtoc.2424 浏览次数: 8656
评审: Neelanjan BoseAnonymous reviewer(s)
Abstract
The Caenorhabditis elegans germ line is an important model system for the study of germ stem cells. Wild-type C. elegans germ cells are syncytial and therefore cannot be isolated in in vitro cultures. In contrast, the germ cells from tumorous mutants can be fully cellularized and isolated intact from the mutant animals. Here we describe a detailed protocol for the isolation of germ cells from tumorous mutants that allows the germ cells to be maintained for extended periods in an in vitro primary culture. This protocol has been adapted from Chaudhari et al., 2016.
Keywords: C. elegans (秀丽隐杆线虫)Background
C. elegans hermaphrodite germ cells are generated in two adult stem cell niches located in the distal regions of the two gonad arms (Hansen and Schedl, 2013; Kimble and Seidel, 2013). In wild-type hermaphrodites, mitotic germ cells are restricted to the distal, stem cell niche regions of the gonad arms. Wild-type germ cells are syncytial, and contain an opening to a common cytoplasm that extends through the central region of the gonad arms. C. elegans tumorous germline mutants have increased mitotic proliferation of germ cells throughout the gonad. We discovered that tumorous germline mutants generally have fully cellularized germ cells that contain intact plasma membranes (Chaudhari et al., 2016). This cellularization allows the isolation of the germ cells and their maintenance in culture. This protocol describes the methodology and tissue culture medium to isolate and maintain germ cells from tumorous mutants in culture. While a culture medium has been described for the primary culture of C. elegans embryonic and larval cells (Strange et al., 2007; Zhang and Kuhn, 2013), germ cells do not survive in this medium (Chaudhari et al., 2016). We created a culture medium for germ cells that is called CeM1 for ‘C. elegans medium 1’. We anticipate that other iterations of the medium could be given subsequent numbers, e.g., ‘CeM2’. This protocol, first reported in Chaudhari et al., 2016, allows the isolation of essentially pure populations of germ cells and their maintenance in in vitro primary cultures. This culture system can allow new experimental approaches to probe germ cell biology in C. elegans.
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版权信息
© 2017 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Vagasi, A. S., Rahman, M. M., Chaudhari, S. N. and Kipreos, E. T. (2017). Primary Culture System for Germ Cells from Caenorhabditis elegans Tumorous Germline Mutants. Bio-protocol 7(15): e2424. DOI: 10.21769/BioProtoc.2424.
分类
干细胞 > 生殖细胞 > 体外培养
细胞生物学 > 细胞分离和培养 > 细胞分离
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