| Literature DB >> 18635811 |
J Tristan Dobson1, Jake Seibert, Evelyn M Teh, Sahar Da'as, Robert B Fraser, Barry H Paw, Tong-Jun Lin, Jason N Berman.
Abstract
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 cepbalpha, identifying these early MCs as a distinct myeloid population arising from a common granulocyte/monocyte progenitor. Morpholino "knock-down" 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.Entities:
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Year: 2008 PMID: 18635811 DOI: 10.1182/blood-2008-03-145011
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113