Here it is shown that the phenotype of adult mice lacking the first enhancer (DNA hypersensitive site I) and the distal promoter of the GATA-1 gene (neoΔHS or GATA-1low mutants) reveals defects in mast cell development. These include the presence of morphologically abnormal alcian blue+ mast cells and apoptotic metachromatic− mast cell precursors in connective tissues and peritoneal lavage and numerous (60–70% of all the progenitors) “unique” trilineage cells committed to erythroid, megakaryocytic, and mast pathways in the bone marrow and spleen. These abnormalities, which were mirrored by impaired mast differentiation in vitro, were reversed by retroviral-mediated expression of GATA-1 cDNA. These data indicate an essential role for GATA-1 in mast cell differentiation.
GATA-1 as a Regulator of Mast Cell Differentiation Revealed by the Phenotype of the GATA-1low Mouse Mutant
Abbreviations used in this paper: BFU, burst-forming unit; BMMC, bone marrow–derived mast cells; E, erythroid; EPO, erythropoietin; GM, granulocytic-monocytic; MC-CPA, mast cell carboxypeptidase A; Mk, megakaryocytic; PGK, phosphoglicerate kinase gene; SCF, stem cell factor; TPO, thrombopoietin; TUNEL, terminal deoxy transferase uridine triphosphate nick-end labeling.
Anna Rita Migliaccio, Rosa Alba Rana, Massimo Sanchez, Rodolfo Lorenzini, Lucia Centurione, Lucia Bianchi, Alessandro Maria Vannucchi, Giovanni Migliaccio, Stuart H. Orkin; GATA-1 as a Regulator of Mast Cell Differentiation Revealed by the Phenotype of the GATA-1low Mouse Mutant . J Exp Med 3 February 2003; 197 (3): 281–296. doi: https://doi.org/10.1084/jem.20021149
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