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PMID: 12719731 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Caspase-independent cell death in T lymphocytes.

Nature immunology ·Vol. 4 ·No. 5 ·2003-05-00 ·Pages 416-23

Jäättelä M, Tschopp J

Abstract

T lymphocyte death is essential for proper function of the immune system. During the decline of an immune response, most of the activated T cells die. Cell death is also responsible for eliminating autoreactive lymphocytes. Although recent studies have focused on caspase-dependent apoptotic signals, much evidence now shows that caspase- independent, necrotic cell death pathways are as important. An understanding of the molecular control of these alternative pathways is beginning to emerge. Damage of organelles including mitochondria, endoplasmic reticulum or lysozymes, leading to an increase in calcium and reactive oxygen species and the release of effector proteins, is frequently involved in caspase-independent cell death.

MeSH Terms
Animals Antigens, CD/physiology Apoptosis/physiology Calcium Signaling Caspases/metabolism Cell Death/physiology Endoplasmic Reticulum/physiology Humans Lysosomes/physiology Mice Mitochondria/physiology Models, Biological Receptors, Tumor Necrosis Factor/physiology Receptors, Tumor Necrosis Factor, Type I T-Lymphocytes/cytology,enzymology,immunology fas Receptor/physiology
Chemicals
Antigens, CD Receptors, Tumor Necrosis Factor Receptors, Tumor Necrosis Factor, Type I fas Receptor Caspases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Jäättelä Marja
Apoptosis Laboratory, Institute of Cancer Biology, Danish Cancer Society, Strandboulevarden 49, DK-2100 Copenhagen, Denmark. mhj@biobase.dk
Tschopp Jürg
Article Info
Journal
Nature immunology
Abbr.
Nat Immunol
ISSN
1529-2908
Published
2003-05-00
Pages
416-23
Language
English
Region
United States
NLM ID
100941354
Subset
IM
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