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Proc Natl Acad Sci U S A. 2003 Jan 21;100(2):556-61. Epub 2003 Jan 8.

Impaired B cell development and function in mice with a targeted disruption of the homeobox gene Hex.

Author information

1
Yale Child Health Research Center, Department of Pediatrics, Yale University School of Medicine, New Haven, CT 06519, USA. clifford.bogue@yale.edu

Abstract

Hex is a homeobox gene that is expressed in all stages of B cell development except plasma cells. We studied lymphocyte development in the absence of Hex by using the RAG1-deficient blastocyst complementation system because homozygous disruption of Hex is embryonic lethal. Hex(-/-);RAG1(-/-) chimeric mice had severely reduced numbers of mature B cells, pre-B cells, and CD5(+) B cells with a striking 15-fold increase in the percentage of B220(-)CD19(+) cells in the bone marrow. Hex(-/-);RAG1(-/-) chimeric mice failed to generate IgG antibodies to T cell-independent antigens, although their serum IgM levels and antibody responses to T cell-dependent antigens were intact. Therefore, Hex is necessary for B cell development and function and its absence results in a dramatic increase in B220(-)CD19(+) cells.

PMID:
12522149
PMCID:
PMC141034
DOI:
10.1073/pnas.0236979100
[Indexed for MEDLINE]
Free PMC Article

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