Cell death controlling complexes and their potential therapeutic role

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• 作者：Alexey V. Zamaraev ; Gelina S. Kopeina…
• 关键词：Cell death ; Protein complexes ; DISC ; Apoptosome ; PIDDosome ; RIPoptosome ; Caspases
• 刊名：Cellular and Molecular Life Sciences (CMLS)
• 出版年：2015
• 出版时间：February 2015
• 年：2015
• 卷：72
• 期：3
• 页码：505-517
• 全文大小：566 KB
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• 作者单位：Alexey V. Zamaraev (1)
  Gelina S. Kopeina (1)
  Boris Zhivotovsky (1) (2)
  Inna N. Lavrik (1) (3)
  
  1. Faculty of Basic Medicine, MV Lomonosov Moscow State University, 119991, Moscow, Russia
  2. Division of Toxicology, Institute of Environmental Medicine, Karolinska Institutet, Box 210, 171 77, Stockholm, Sweden
  3. Department of Translational Inflammation, Institute of Experimental Internal Medicine, Otto von Guericke University, Magdeburg, Germany
  
• 刊物类别：Biomedical and Life Sciences
• 刊物主题：Life Sciences
  Cell Biology
  Biomedicine
  Life Sciences
  Biochemistry
  
• 出版者：Birkh盲user Basel
• ISSN：1420-9071

文摘

Programmed cell death plays a central role in the regulation of homeostasis and development of multicellular organisms. Deregulation of programmed cell death is connected to a number of disorders, including cancer and autoimmune diseases. Initiation of cell death occurs in the multiprotein complexes or high molecular weight platforms. Composition, structure, and molecular interactions within these platforms influence the cellular decision toward life or death and, therefore, define the induction of a particular cell death program. Here, we discuss in detail the key cell-death complexes—including DISC, complex II, and TNFRI complex I/II, and the necrosome, RIPoptosome, apoptosome, and PIDDosome—that control apoptosis or necroptosis pathways as well as their regulation. The possibility of their pharmacological targeting leading to the development of new strategies of interference with cell death programs via control of the high molecular weight platforms will be discussed.