Cognate antigen induced apoptosis of thymocytes and peripheral T cells

1997 ◽  
Vol 56 (1-3) ◽  
pp. 82
Author(s):  
A Wack
1997 ◽  
Vol 56 ◽  
pp. 82
Author(s):  
A. Wack ◽  
O. Williams ◽  
P. Corbella ◽  
I.N. Crispe ◽  
D. Kioussis

1996 ◽  
Vol 183 (4) ◽  
pp. 1789-1796 ◽  
Author(s):  
G Süss ◽  
K Shortman

Dendritic cells (DC), the most efficient antigen-presenting cells, are well equipped for activation of naive CD4+ T cells by their expression of high levels of major histocompatibility complex and costimulator molecules. We now demonstrate that some DC are equally well equipped for killing these same T cells. Murine splenic DC consist of both conventional CD8alpha- DC and a major population of CD8alpha+ DC. Whereas CD8- DC induce a vigorous proliferative response in CD4 T cells, CD8+ DC induce a lesser response that is associated with marked T cell apoptosis. By using various mixtures of T cells and DC from Fas-mutant lpr/lpr mice and Fas-ligand (FasL) mutant gld/gld mice, we show this death is due to interaction of Fas on activated T cells with FasL on CD8+ DC. Furthermore, we show by direct surface staining that CD8+ DC, but not CD8- DC, express FasL at high levels. These findings indicate that FasL+ CD8+ DC are a specialized subgroup of DC with a role in the regulation of the response of primary peripheral T cells.


1997 ◽  
Vol 29 (5) ◽  
pp. 2377-2378 ◽  
Author(s):  
M. Rouleau ◽  
B. Mollereau ◽  
A. Bernard ◽  
D. Metivier ◽  
M.A. Rosenthal-Allieri ◽  
...  

2004 ◽  
Vol 173 (7) ◽  
pp. 4407-4416 ◽  
Author(s):  
Wen Yang ◽  
Shabbir Hussain ◽  
Qing-Sheng Mi ◽  
Pere Santamaria ◽  
Terry L. Delovitch

2002 ◽  
Vol 9 (4) ◽  
pp. 197-202 ◽  
Author(s):  
Friedrich Haag ◽  
Dunja Freese ◽  
Felix Scheublein ◽  
Wiebke Ohlrogge ◽  
Sahil Adriouch ◽  
...  

Extracellular nucleotides such as ATP and NAD can profoundly affect the functions of lymphocytes, macrophages, and other cells. We have recently shown that extracellular NAD induces rapid apoptosis in naive T cells by a mechanism involving the ADP-ribosylation of cell surface molecules. In the present paper, we describe that T cells of different developmental stages differ in their sensitivity to NAD-induced apoptosis. Thymocytes were less susceptible than peripheral lymph node T cells, and freshly activated cells were more resistant than resting cells. Sensitivity to NAD-induced apoptosis generally correlated with expression of the ADP-ribosyltransferase ART2.2, which is not expressed on thymocytes and shed from peripheral T cells upon activation. Our findings suggest that NAD-induced apoptosis does not play a role during thymic selection of T cells, but rather may play a role by preventing the activation of unwanted bystander T cells during an immune response, and thus may participate in the control of autoimmunity.


1996 ◽  
Vol 183 (5) ◽  
pp. 2355-2360 ◽  
Author(s):  
S Noda ◽  
A Kosugi ◽  
S Saitoh ◽  
S Narumiya ◽  
T Hamaoka

During T cell development in the thymus, the expression of thymic shared antigen-1 (TSA-1)/stem cell antigen-2 (Sca-2), a glycosylphosphatidylinositol (GPI)-anchored differentiation antigen, is developmentally regulated. The expression level of TSA-1 is the highest in most immature CD4- CD8- thymocytes, high in CD4+ CD8+ thymocytes, but barely detectable in mature CD4+ CD8- or CD4- CD8- thymocytes and peripheral T cells. We have previously shown that surface TSA-1 expression in peripheral T cells is induced upon activation and that anti-TSA-1 mAb inhibits the T cell receptor (TCR) signaling pathway in activated T cells. In the present study, we have analyzed a role of TSA-1 in thymic selection events, especially in TCR-mediated apoptosis. In in vitro experiments, anti-TSA-1 blocked anti-CD3-induced cell death of T cell hybridomas. When anti-TSA-1 was injected into newborn mice in vivo together with anti-CD3 epsilon or anti-TCR-beta, TCR/CD3-mediated apoptosis of thymocytes was almost completely blocked. The blockade of apoptosis was defined by the inhibition of, first, the decrease in total number of thymocytes; second, the decrease in percentages of CD4+ CD8+ thymocytes; and third, the induction of DNA fragmentation. However, anti-TSA-1 did not block either steroid- or radiation-induced apoptosis, indicating that a signal via TSA-1 does not inhibit a common pathway of thymocyte apoptosis. Since TCR-mediated apoptosis is pivotal in thymic ontogeny, these results suggest that TSA-1/Sca-2 is an important cell surface molecule regulating the fate of a developing T cell.


2001 ◽  
Vol 257 (1-2) ◽  
pp. 71-82 ◽  
Author(s):  
J Fishman-Lobell ◽  
P Tsui ◽  
M Reddy ◽  
R DiPrinzio ◽  
C Eichman ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document