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Publication : Genetic analyses of NFKB1 and OCA-B function: defects in B cells, serum IgM level, and antibody responses in Nfkb1-/-Oca-b-/- mice.

First Author  Kim U Year  2000
Journal  J Immunol Volume  165
Issue  12 Pages  6825-32
PubMed ID  11120805 Mgi Jnum  J:66173
Mgi Id  MGI:1928057 Doi  10.4049/jimmunol.165.12.6825
Citation  Kim U, et al. (2000) Genetic analyses of NFKB1 and OCA-B function: defects in B cells, serum IgM level, and antibody responses in Nfkb1(-/-)Oca-b(-/-) mice. J Immunol 165(12):6825-32
abstractText  Defined patterns of gene expression during cell differentiation are likely to be ensured by multiple factors playing redundant roles. By generating mice deficient in both NFKB1 and OCA-B, we show here that the two transcription factors are required for B-1 cell differentiation and serum IgM production. In addition, relative to Nfkb1(-/-) or Oca-b(-/-) mice, the Nfkb1(-/-)Oca-b(-/-) mice show a decrease in conventional B cell frequencies in the spleen and augmented reductions in T-independent and T-dependent Ab responses. These results suggest that NFKB1 and OCA-B play compensatory roles in multiple aspects of B cell differentiation.
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