Andera Ladislav
Institute of Molecular Genetics AS CR, Videnska, Prague, Czech Republic.
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2009 Sep;153(3):173-80. doi: 10.5507/bp.2009.029.
The fine balance in cellular life and death is affected by a number of tightly regulated, direct signals that can help to turn the balance either in favor of or against the ultimate fate. Among the most prominent players in the field of the extracellular signals leading to cell death, preferentially through induction of apoptosis belong several receptors from so-called Death Receptors group of the Tumour Necrosis Factors Receptors (TNFR) family.
Over 15 years of the research on activation and regulation of the most prominent member of this group - receptors for the ligands TRAIL, FasL and TNFalpha brought not only a detail (and still refining) mechanism of these receptors activation and downstream signaling, but also connected them with the ultimate apoptotic gatekeeper - mitochondria. Mitochondria are, in addition to their essential role as the energy factories also repositories of a cavalry of apoptosis-inducing as well as regulatory proteins. However, in addition to the pro-death signaling, these receptors were also shown under certain circumstances to activate an opposite, pro-proliferative signaling as well as to participate in pro-inflammatory responses.
Thus despite the concerned effort of a number of groups and thousands of published papers, novel roles for the intriguing group of these receptors and their ligands and fine tuning of their signaling still await to be uncovered. This cut-through review will be mainly focused on the prominent death-inducing members of this group - TNFR1, Fas/CD95 and TRAIL receptors.
细胞生死的微妙平衡受到许多严格调控的直接信号的影响,这些信号可有助于使平衡朝着有利于或不利于最终命运的方向转变。在导致细胞死亡的细胞外信号领域中,最突出的参与者之一是肿瘤坏死因子受体(TNFR)家族中所谓死亡受体组的几种受体,它们优先通过诱导细胞凋亡发挥作用。
对该组中最突出成员——TRAIL、FasL和TNFα配体的受体进行了超过15年的激活和调控研究,不仅揭示了这些受体激活和下游信号传导的详细(且仍在完善)机制,还将它们与最终的凋亡守门人——线粒体联系起来。线粒体除了作为能量工厂发挥重要作用外,还是一系列凋亡诱导蛋白和调节蛋白的储存库。然而,除了促死亡信号传导外,这些受体在某些情况下还被证明可激活相反的促增殖信号传导,并参与促炎反应。
因此,尽管许多研究团队付出了努力且发表了数千篇论文,但这些受体及其配体这一有趣的群体的新作用以及它们信号传导的精细调节仍有待发现。本综述将主要聚焦于该组中突出的诱导死亡成员——TNFR1、Fas/CD95和TRAIL受体。