2011Molecular BiologyRequires access

Regulation of death receptor-induced apoptosis induced via CD95/Fas and other death receptors

Inna N. Lavrik

Open publisher page 17 citations

Abstract

Apoptosis (programmed cell death) is common to all multicellular organisms. Apoptosis can be triggered by the extrinsic (death receptor (DR)) or the intrinsic (mitochondrial) death pathways. Apoptosis plays the central role for the cell differentiation, removal of the damaged cells and the homeostasis of the immune system. CD95 (APO-1/Fas) is a member of the DR family, which was discovered more than 20 years ago. This review is focused on the mechanisms of DR-induced apoptosis focusing on CD95 (APO-1/Fas)-mediated apoptosis and the role of the anti-apoptotic protein c-FLIP in the extrinsic apoptosis. Regulation of apoptosis plays the central role in the immune system and apoptosis deregulation leads to a number of diseases. Gaining insights into these processes will improve our understanding of the pathogenesis of diseases such as cancer, autoimmunity and AIDS, and will open new approaches to rational treatment strategies.

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What this paper is about

Apoptosis (programmed cell death) is common to all multicellular organisms. Apoptosis can be triggered by the extrinsic (death receptor (DR)) or the intrinsic (mitochondrial) death pathways. Apoptosis plays the central role for the cell differentiation, removal of the damaged cells and the homeostasis of the immune system. CD95 (APO-1/Fas) is a member of the DR family, which was discovered more than 20 years ago. This review is focused on the mechanisms of DR-induced apoptosis focusing on CD95 (APO-1/Fas)-mediated apoptosis and the role of the anti-apoptotic protein c-FLIP in the extrinsic apoptosis. Regulation of apoptosis plays the central role in the immune system and apoptosis deregulation leads to a number of diseases. Gaining insights into these processes will improve our understanding of the pathogenesis of diseases such as cancer, autoimmunity and AIDS, and will open new approaches to rational treatment strategies.

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OpenAlex reports 17 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

Apoptosis (programmed cell death) is common to all multicellular organisms. Apoptosis can be triggered by the extrinsic (death receptor (DR)) or the intrinsic (mitochondrial) death pathways. Apoptosis plays the central role for the cell differentiation, removal of the damaged cells and the homeostasis of the immune system. CD95 (APO-1/Fas) is a member of the DR family, which was discovered more than 20 years ago. This review is focused on the mechanisms of DR-induced apoptosis focusing on CD95 (APO-1/Fas)-mediated apoptosis and the role of the anti-apoptotic protein c-FLIP in the extrinsic apoptosis. Regulation of apoptosis plays the central role in the immune system and apoptosis deregulation leads to a number of diseases. Gaining insights into these processes will improve our understanding of the pathogenesis of diseases such as cancer, autoimmunity and AIDS, and will open new approaches to rational treatment strategies.

Key concepts: Fas receptor, Apoptosis, Programmed cell death, Cell biology, Receptor, Biology, Fas ligand, Immune system

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