A 39-kDa protein on activated helper T cells binds CD40 and transduces the signal for cognate activation of B cells

Details

Serval ID
serval:BIB_5CAD71A1D5BC
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
A 39-kDa protein on activated helper T cells binds CD40 and transduces the signal for cognate activation of B cells
Journal
Proceedings of the National Academy of Sciences of the United States of America
Author(s)
Noelle  R. J., Roy  M., Shepherd  D. M., Stamenkovic  I., Ledbetter  J. A., Aruffo  A.
ISSN
0027-8424 (Print)
Publication state
Published
Issued date
1992
Volume
89
Number
14
Pages
6550-6554
Notes
PT - In Vitro PT - Journal Article PT - Research Support, U.S. Gov't, P.H.S
Abstract
CD40 is a B-cell surface molecule that has been shown to induce B-cell growth upon ligation with monoclonal antibodies. This report shows that triggering via CD40 is essential for the activation of resting B cells by helper T cells (Th). A soluble fusion protein of CD40 and human immunoglobulin, CD40-Ig, inhibited the induction of B-cell cycle entry, proliferation, and differentiation by activated Th1 and Th2. The ligand for CD40 was identified as a 39-kDa membrane protein that was selectively expressed on activated Th. A monoclonal antibody specific for the 39-kDa protein inhibited CD40-Ig binding and also inhibited the activation of B cells by Th. These data indicate that the 39-kDa membrane protein expressed on activated Th is a binding protein for CD40 and functions to transduce the signal for Th-dependent B-cell activation
Keywords
Animals/Antibodies/Antibodies,Monoclonal/Antibody Formation/Antigens/Antigens,CD/Antigens,CD40/Antigens,Differentiation,B-Lymphocyte/Antigens,Surface/B-Lymphocytes/Cell Cycle/Cell Differentiation/cytology/immunology/Lymphocyte Activation/Lymphocyte Cooperation/Membrane Proteins/metabolism/Mice/Mice,Inbred DBA/physiology/Protein Binding/Proteins/Research/Signal Transduction/T-Lymphocytes,Helper-Inducer
Pubmed
Web of science
Create date
29/01/2008 19:35
Last modification date
20/08/2019 15:15
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