Carboxypeptidase A5 identifies a novel mast cell lineage in the zebrafish providing new insight into mast cell fate determination

被引:105
作者
Dobson, J. Tristan [2 ]
Seibert, Jake
Teh, Evelyn M. [2 ]
Da'as, Sahar
Fraser, Robert B. [3 ]
Paw, Barry H. [4 ,5 ]
Lin, Tong-Jun [2 ]
Berman, Jason N. [1 ,2 ]
机构
[1] Dalhousie Univ, Dept Pediat, Div Pediat Hematol Oncol, IWK Hlth Ctr, Halifax, NS B3K 6R8, Canada
[2] Dalhousie Univ, Dept Microbiol & Immunol, Halifax, NS B3K 6R8, Canada
[3] Dalhousie Univ, Dept Pathol, Halifax, NS B3K 6R8, Canada
[4] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Hematol, Boston, MA 02115 USA
[5] Harvard Univ, Childrens Hosp, Sch Med, Div Hematol Oncol, Boston, MA 02115 USA
基金
加拿大健康研究院;
关键词
D O I
10.1182/blood-2008-03-145011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mast cells (MCs) play critical roles in allergy and inflammation, yet their development remains controversial due to limitations posed by traditional animal models. The zebrafish provides a highly efficient system for studying vertebrate hematopoiesis. We have identified zebrafish MCs in the gill and intestine, which resemble their mammalian counterparts both structurally and functionally. Carboxypeptidase A5 (cpa5), a MC-specific enzyme, is expressed in zebrafish blood cells beginning at 24 hours post fertilization (hpf). At 28 hpf, colocalization is observed with pu.1, mpo, l-plastin, and lysozyme C, but not fms or cepb alpha, identifying these early MCs as a distinct myeloid population arising from a common granulocyte/monocyte progenitor. Morpholino "knockdown" studies demonstrate that transcription factors gata-2 and pu.1, but not gata-1 or fog-1, are necessary for early MC development. These studies validate the zebrafish as an in vivo tool for studying MC ontogeny and function with future capacity for modeling human MC diseases.
引用
收藏
页码:2969 / 2972
页数:4
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