Tubulin Polymerization Modulates Interleukin-2 Receptor Signal Transduction in Human T Cells

2006 ◽  
Vol 26 (1-2) ◽  
pp. 87-106 ◽  
Author(s):  
Jens Goebel ◽  
Kathy Forrest ◽  
Marsha Wills-Karp ◽  
Thomas L. Roszman
1992 ◽  
Vol 53 (1) ◽  
pp. 146-150 ◽  
Author(s):  
BAOGUI LI ◽  
PRABODH K. SEHAJPAL ◽  
AJIT SUBRAMANIAM ◽  
ANTONIO JOSEPH ◽  
KURT H. STENZEL ◽  
...  

1993 ◽  
Vol 294 (2) ◽  
pp. 339-342 ◽  
Author(s):  
G A Evans ◽  
O M Z Howard ◽  
R Erwin ◽  
W L Farrar

The haematopoietic protein, p95vav, has been shown to be a tyrosine kinase substrate and to have tyrosine kinase-modulated guanine-nucleotide-releasing-factor activity. This implies a function in the control of ras or ras-like proteins. Because ras activation has been shown to be a downstream event following stimulation of the interleukin-2 (IL-2) receptor, we investigated the possibility that vav was involved in IL-2 signal transduction pathways, using human T cells as a model. We found rapid tyrosine phosphorylation of vav in response to IL-2 within 1 min, with maximum increase of phosphorylation of 5-fold occurring by 5 min after treatment in normal human T cells. IL-2 stimulation of the human T-cell line YT and a subclone of the YT cell line (YTlck-) that does not express message for the src-family kinase p56lck also results in a rapid rate of tyrosine phosphorylation of vav of more than 5-fold by 5 min. These results suggest that vav may play an important role in IL-2-stimulated signal transduction and that there is not a strict requirement for the tyrosine kinase p56lck.


1989 ◽  
Vol 26 (10) ◽  
pp. 979-984 ◽  
Author(s):  
Stanley C. Jordan ◽  
Mieko Toyoda ◽  
John Prehn ◽  
Jacques M. Lemire ◽  
Rebecca Sakai ◽  
...  

1997 ◽  
Vol 27 (11) ◽  
pp. 2793-2799 ◽  
Author(s):  
Javier Gómez ◽  
Carlos Martínez-A. ◽  
Murielle Giry ◽  
Alphonse García ◽  
Angelita Rebollo

1994 ◽  
Vol 27 (1) ◽  
pp. 43-55 ◽  
Author(s):  
Olcay Ayanlar Batuman ◽  
Ann P. Ferrero ◽  
Arturo Diaz ◽  
Bruce Berger ◽  
Roger J. Pomerantz

1992 ◽  
Vol 175 (4) ◽  
pp. 951-960 ◽  
Author(s):  
P Vandenberghe ◽  
G J Freeman ◽  
L M Nadler ◽  
M C Fletcher ◽  
M Kamoun ◽  
...  

CD28 is an adhesion receptor expressed as a 44-kD dimer on the surface of a major subset of human T cells. The CD28 receptor regulates the production of multiple lymphokines, including interleukin 2 (IL-2), by activation of a signal transduction pathway that is poorly understood. Here we show that ligation of CD28 by a monoclonal antibody (mAb) or by a natural ligand, B7/BB1, induces protein tyrosine phosphorylation that is distinct from T cell receptor (TCR)-induced tyrosine phosphorylation. CD28-induced protein tyrosine phosphorylation was greatly enhanced in cells that had been preactivated by ligation of the TCR, or by pretreatment with phorbol esters. Rapid and prolonged tyrosine phosphorylation of a single substrate, pp100, was induced in T cells after interaction with B7/BB1 presented on transfected Chinese hamster ovary (CHO) cells. Anti-B7 mAb inhibited B7/BB1 receptor-induced tyrosine phosphorylation, indicating that B7-CD28 interaction was required. CD28-induced tyrosine phosphorylation was independent of the TCR because it occurred in a variant of the Jurkat T cell line that does not express the TCR. Herbimycin A, a protein tyrosine kinase inhibitor, could prevent CD28-induced tyrosine phosphorylation and CD28-induced IL-2 production in normal T cells. The simultaneous crosslinking of CD28 and CD45, a tyrosine phosphatase, could prevent tyrosine phosphorylation of pp100. These results suggest that specific tyrosine phosphorylation, particularly of pp100, occurs directly as a result of CD28 ligand binding and is involved in transducing the signal delivered through CD28 by accessory cells that express the B7/BB1 receptor. Thus, this particular form of signal transduction may be relevant to lymphokine production and, potentially may provide a means to study the induction of self-tolerance, given the putative role of the costimulatory signal in the induction of T cell activation or anergy.


1985 ◽  
Vol 22 (8) ◽  
pp. 937-947 ◽  
Author(s):  
Steven K. Dower ◽  
Steven H. Hefeneider ◽  
Alan R. Alpert ◽  
David L. Urdal

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