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Science 13 December 1996: Vol. 274. no. 5294, pp. 1906 - 1909 DOI: 10.1126/science.274.5294.1906
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Reports
CD5-Mediated Negative Regulation of Antigen Receptor-Induced
Growth Signals in B-1 B Cells
Gabriel Bikah,
Jacqueline Carey,
John R. Ciallella,
Alexander Tarakhovsky,
Subbarao Bondada
*
A subset of B lymphocytes present primarily in the peritoneal and
pleural cavities is defined by the expression of CD5 and is elevated in
autoimmune diseases. Upon signaling through membrane immunoglobulin M
(mIgM), splenic B lymphocytes (B-2) proliferate, whereas peritoneal B
cells (B-1) undergo apoptosis. However, in CD5-deficient mice, B-1
cells responded to mIgM crosslinking by developing a resistance to
apoptosis and entering the cell cycle. In wild-type B-1 cells,
prevention of association between CD5 and mIgM rescued their growth
response to mIgM crosslinking. Thus the B cell receptor-mediated
signaling is negatively regulated by CD5 in normal B-1 cells.
G. Bikah, J. Carey, J. R. Ciallella, S. Bondada, Department of
Microbiology and Immunology and Center on Aging, University of
Kentucky, Lexington, KY 40536, USA.
A. Tarakhovsky, Institute for Genetics, University of Cologne, 50937 Cologne, Germany.
*
To whom correspondence should be addressed. E-mail:
sbonda{at}pop.uky.edu
Read the Full Text
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