3BP2 deficiency impairs the response of B cells, but not T cells, to antigen receptor ligation.

Abstract:

:The adapter protein 3BP2 is expressed in lymphocytes; binds to Syk/ZAP-70, Vav, and phospholipase C-gamma (PLC-gamma); and is thought to be important for interleukin-2 gene transcription in T cells. To define the role of 3BP2 in lymphocyte development and function, we generated 3BP2-deficient mice. T-cell development, proliferation, cytokine secretion, and signaling in response to T-cell receptor (TCR) ligation were all normal in 3BP2(-/-) mice. 3BP2(-/-) mice had increased accumulation of pre-B cells in the bone marrow and a block in the progression of transitional B cells in the spleen from the T1 to the T2 stage, but normal numbers of mature B cells. B-cell proliferation, cell cycle progression, PLC-gamma2 phosphorylation, calcium mobilization, NF-ATp dephosphorylation, and Erk and Jnk activation in response to B-cell receptor (BCR) ligation were all impaired. These results suggest that 3BP2 is important for BCR, but not for TCR signaling.

journal_name

Mol Cell Biol

authors

de la Fuente MA,Kumar L,Lu B,Geha RS

doi

10.1128/MCB.00087-06

subject

Has Abstract

pub_date

2006-07-01 00:00:00

pages

5214-25

issue

14

eissn

0270-7306

issn

1098-5549

pii

26/14/5214

journal_volume

26

pub_type

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