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凋亡中的鞘脂

Sphingolipids in apoptosis.

作者信息

Tirodkar T S, Voelkel-Johnson C

机构信息

Department of Microbiology & Immunology, Medical University of South Carolina, Charleston, SC 29425, USA.

出版信息

Exp Oncol. 2012 Oct;34(3):231-42.

Abstract

Forty years ago, the term "apoptosis" was introduced to describe a form of programmed cell death. Key players that mediate apoptosis at the molecular level such as caspases, death receptors, Bcl-2 family members have since been identified and their regulation remains a research focus of many laboratories. In 1993, approximately 20 years after the introduction of apoptosis, the sphingolipid ceramide was first linked to this form of cell death. Sphingolipids are bioactive components of cellular membranes that are involved in numerous physiological functions. In this paper, we discuss the inherent complexities of sphingolipid signaling and elaborate on how sphingolipids, primarily ceramide, influence apoptotic events such as death receptor aggregation in the plasma membrane and pore formation at the mitochondria. Possible roles of sphingolipids in other subcellular compartments, such as the nucleus, endoplasmic reticulum and lysosomes are also discussed. We conclude by summarizing the recent developments in sphingolipid based cancer therapy. This article is part of a Special Issue entitled "Apoptosis: Four Decades Later".

摘要

四十年前,“凋亡”一词被引入以描述一种程序性细胞死亡形式。自那时起,在分子水平介导凋亡的关键因子,如半胱天冬酶、死亡受体、Bcl-2家族成员已被确定,其调控仍是许多实验室的研究重点。1993年,在凋亡概念提出约20年后,鞘脂类神经酰胺首次与这种细胞死亡形式联系起来。鞘脂类是细胞膜的生物活性成分,参与众多生理功能。在本文中,我们讨论了鞘脂信号传导的内在复杂性,并详细阐述了鞘脂类,主要是神经酰胺,如何影响凋亡事件,如质膜上死亡受体的聚集和线粒体上孔的形成。还讨论了鞘脂类在其他亚细胞区室,如细胞核、内质网和溶酶体中的可能作用。我们通过总结基于鞘脂类的癌症治疗的最新进展来得出结论。本文是名为“凋亡:四十年后”的特刊的一部分。

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