Characterization of immune-matched hematopoietic transplantation in zebrafish

被引:34
作者
de Jong, Jill L. O. [1 ,2 ,3 ]
Burns, Caroline Erter [1 ,2 ,3 ]
Chen, Aye T. [1 ,2 ,3 ]
Pugach, Emily [1 ,2 ,3 ]
Mayhall, Elizabeth A. [1 ,2 ,3 ]
Smith, Alexandra C. H. [1 ,2 ,3 ]
Feldman, Henry A. [4 ]
Zhou, Yi [1 ,2 ,3 ]
Zon, Leonard I. [1 ,2 ,3 ]
机构
[1] Harvard Univ, Sch Med, Childrens Hosp Boston, Div Hematol Oncol,Harvard Stem Cell Inst, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Stem Cell Program, Harvard Stem Cell Inst, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dana Farber Canc Inst, Harvard Stem Cell Inst,Howard Hughes Med Inst, Boston, MA 02115 USA
[4] Childrens Hosp Boston, Clin Res Program, Boston, MA USA
基金
美国国家卫生研究院;
关键词
MHC CLASS-I; MUTATIONS; LINEAGE;
D O I
10.1182/blood-2010-09-307488
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Evaluating hematopoietic stem cell (HSC) function in vivo requires a long-term transplantation assay. Although zebrafish are a powerful model for discovering the genetics of hematopoiesis, hematopoietic transplantation approaches have been underdeveloped. Here we established a long-term reconstitution assay in adult zebrafish. Primary and secondary recipients showed multilineage engraftment at 3 months after transplantation. Limiting dilution data suggest that at least 1 in 65 000 zebrafish marrow cells contain re-populating activity, consistent with mammalian HSC frequencies. We defined zebrafish haplotypes at the proposed major histocompatibility complex locus on chromosome 19 and tested functional significance through hematopoietic transplantation. Matching donors and recipients dramatically increased engraftment and percentage donor chimerism compared with unmatched fish. These data constitute the first functional test of zebrafish histocompatibility genes, enabling the development of matched hematopoietic transplantations. This lays the foundation for competitive transplantation experiments with mutant zebrafish HSCs and chemicals to test for effects on engraftment, thereby providing a model for human hematopoietic diseases and treatments not previously available. (Blood. 2011;117(16):4234-4242)
引用
收藏
页码:4234 / 4242
页数:9
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