Caspase 3 is not essential for the induction of anergy or multiple pathways of CD8+ T-cell death.

Abstract:

:T-cell death is a fundamental process that is intricately regulated at multiple phases during T-cell differentiation, tolerance induction and the decline of the immune response. Caspase 3 is a crucial molecule regulating both mitochondrial and death receptor apoptotic pathways and therefore we were interested in examining the role of caspase 3 in T cells. Using P14 and H-Y CD8(+) TCR-transgenic models, our analysis has shown that caspase 3 is not required for thymic negative selection. In addition, caspase 3 does not play a prominent role in the contraction phase following acute viral infection, nor clonal deletion of CD8(+) T cells under tolerizing conditions. Surprisingly, our studies demonstrate that caspase 3 was not required for the induction of CD8(+) T-cell anergy in vivo, contrary to published reports using CD4(+) T cells. Therefore, these results demonstrate that caspase 3 is not essential in CD8(+) T cells for multiple forms of thymic or peripheral tolerance, nor the contraction phase after an acute anti-viral response.

journal_name

Eur J Immunol

authors

Murakami K,Liadis N,Sarmiento J,Elford AR,Woo M,Nguyen LT,Mak TW,Ohashi PS

doi

10.1002/eji.201040475

subject

Has Abstract

pub_date

2010-12-01 00:00:00

pages

3372-7

issue

12

eissn

0014-2980

issn

1521-4141

journal_volume

40

pub_type

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