TY - JOUR
T1 - Carboxypeptidase A5 identifies a novel mast cell lineage in the zebrafish providing new insight into mast cell fate determination
AU - Dobson, J. Tristan
AU - Seibert, Jake
AU - Teh, Evelyn M.
AU - Da'as, Sahar
AU - Fraser, Robert B.
AU - Paw, Barry H.
AU - Lin, Tong Jun
AU - Berman, Jason N.
PY - 2008/10/1
Y1 - 2008/10/1
N2 - 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 tms or cepba, 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,
AB - 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 tms or cepba, 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,
UR - http://www.scopus.com/inward/record.url?scp=53449087370&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=53449087370&partnerID=8YFLogxK
U2 - 10.1182/blood-2008-03-145011
DO - 10.1182/blood-2008-03-145011
M3 - Article
C2 - 18635811
AN - SCOPUS:53449087370
SN - 0006-4971
VL - 112
SP - 2969
EP - 2972
JO - Blood
JF - Blood
IS - 7
ER -