Ex vivo tools for the clonal analysis of zebrafish hematopoiesis

被引:18
|
作者
Svoboda, Ondrej [1 ]
Stachura, David L. [2 ]
Machonova, Olga [1 ]
Zon, Leonard I. [3 ,4 ,5 ]
Traver, David [6 ]
Bartunek, Petr [1 ]
机构
[1] AS CR, Inst Mol Genet, Dept Cell Differentiat, Vvi, Prague, Czech Republic
[2] Calif State Univ Chico, Dept Biol Sci, Chico, CA 95929 USA
[3] Dana Farber Boston Childrens, Stem Cell Program, Boston, MA USA
[4] Dana Farber Boston Childrens, Div Hematol Oncol, Boston, MA USA
[5] Harvard Univ, Sch Med, Howard Hughes Med Inst, Harvard Stem Cell Inst, Boston, MA 02115 USA
[6] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
IN-VITRO; VERTEBRATE HEMATOPOIESIS; STEM-CELLS; FISH; IDENTIFICATION; DISSECTION; SYSTEMS; MODELS; CANCER; GENE;
D O I
10.1038/nprot.2016.053
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This protocol describes the ex vivo characterization of zebrafish hematopoietic progenitors. We show how to isolate zebrafish hematopoietic cells for cultivation and differentiation in colony assays in semi-solid media. We also describe procedures for the generation of recombinant zebrafish cytokines and for the isolation of carp serum, which are essential components of the medium required to grow zebrafish hematopoietic cells ex vivo. The outcome of these clonal assays can easily be evaluated using standard microscopy techniques after 3-10 d in culture. In addition, we describe how to isolate individual colonies for further imaging and gene expression profiling. In other vertebrate model organisms, ex vivo assays have been crucial for elucidating the relationships among hematopoietic stem cells (HSCs), progenitor cells and their mature progeny. The present protocol should facilitate such studies on cells derived from zebrafish.
引用
收藏
页码:1007 / 1020
页数:14
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