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Cited by 292

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

NF-κB RelA-deficient Lymphocytes: Normal Development of T Cells and B Cells, Impaired Production of IgA and IgG1 and Reduced Proliferative Responses

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Doi, Takahiro S., Takahashi, Toshitada, Taguchi, Osamu, Azuma, Takachika, Obata, Yuichi·1997·The Journal of Experimental Medicine

Abstract

To investigate the function of NF-κB RelA (p65), we generated mice deficient in this NF-κB family member by homologous recombination. Mice lacking RelA showed liver degeneration and died around embryonic day 14.5. To elucidate the role of RelA in lymphocyte development and function, we transplanted fetal liver cells of 13.5-day embryos from heterozygote matings into irradiated SCID mice. Within 4 weeks, both T and B cells had developed in the SCID mice receiving relA−/− fetal liver transplants, similar to the relA+/+ and +/− cases. T cells were found to mature to Thy-1+/TCRαβ+/CD3+/CD4+ or CD8+, while B cells had the ability to differentiate to IgM+/B220+ and to secrete immunoglobulins. However, the secretion of IgG1 and IgA was reduced in RelA-deficient B cells. Furthermore, both T and B cells lacking RelA showed marked reduction in proliferative responses to stimulation with Con A, anti-CD3, anti-CD3+anti-CD28, LPS, anti-IgM, and PMA+calcium ionophore. The results indicate that RelA plays a critical role in production of specific Ig isotypes and also in signal transduction pathways for lymphocyte proliferation.

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Metadata

Authors
Doi, T. S., Takahashi, T., Taguchi, O., Azuma, T., & Obata, Y.
Venue
The Journal of Experimental Medicine
Published
1997-03-03
Volume
185
Issue
5
Pages
953-962
ISSN
  • 0022-1007 (ISSN-L)
  • 1540-9538
OpenAlex
W2150038520
Cited by
292
References
2
FWCI
10.03
Type
journal article
Language
en
Open access
bronze

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