Volume 9, Issue 4 427843 pp. 197-202
Article
Open Access

T Cells of Different Developmental Stages Differ in Sensitivity to Apoptosis Induced by Extracellular NAD

Friedrich Haag

Friedrich Haag

Institute of Immunology University Hospital Martinistr. 52 Hamburg D-20246, Germany , uni-hamburg.de

Search for more papers by this author
Dunja Freese

Dunja Freese

Institute of Immunology University Hospital Martinistr. 52 Hamburg D-20246, Germany , uni-hamburg.de

Search for more papers by this author
Felix Scheublein

Felix Scheublein

Institute of Immunology University Hospital Martinistr. 52 Hamburg D-20246, Germany , uni-hamburg.de

Search for more papers by this author
Wiebke Ohlrogge

Wiebke Ohlrogge

Institute of Immunology University Hospital Martinistr. 52 Hamburg D-20246, Germany , uni-hamburg.de

Search for more papers by this author
Sahil Adriouch

Sahil Adriouch

Laboratoire d′Immunodifferenciation, EA 1556 Université Denis Diderot Paris 7 CP Tour 54 2 place Jussieu Paris Cedex 05 75251, France , univ-paris-diderot.fr

Search for more papers by this author
Michel Seman

Michel Seman

Laboratoire d′Immunodifferenciation, EA 1556 Université Denis Diderot Paris 7 CP Tour 54 2 place Jussieu Paris Cedex 05 75251, France , univ-paris-diderot.fr

Search for more papers by this author
Friedrich Koch-Nolte

Friedrich Koch-Nolte

Institute of Immunology University Hospital Martinistr. 52 Hamburg D-20246, Germany , uni-hamburg.de

Search for more papers by this author
First published: 01 January 2002
Citations: 16

Abstract

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.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.