Sphingolipids and cell death

被引:201
作者
Morales, Albert
Lee, Hyunmi
Goni, Felix M.
Kolesnick, Richard
Fernandez-Checa, Jose C. [1 ]
机构
[1] IDIBAPS, CIBER HEPAD, Hosp Clin & Prov, IMDiM,Liver Unit, E-08036 Barcelona, Spain
[2] IDIBAPS, CIBER HEPAD, Hosp Clin & Prov, IMDiM,Ctr Invest Biomed Esther Koplowitz, E-08036 Barcelona, Spain
[3] CSIC, Inst Invest Biomed, Dept Cell Death & Proliferat, E-08036 Barcelona, Spain
[4] Mem Sloan Kettering Canc Ctr, Lab Signal Transduct, New York, NY 10021 USA
[5] Univ Basque Country, Ctr Mixto CSIC, Unidad Biofis, E-48080 Bilbao, Spain
[6] Univ Basque Country, Dept Bioquim, E-48080 Bilbao, Spain
关键词
ceramide; gangliosides; membranes; transbilayer trafficking; mitochondria; endoplasmic reticulum;
D O I
10.1007/s10495-007-0721-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sphingolipids (SLs) have been considered for many years as predominant building blocks of biological membranes with key structural functions and little relevance in cellular signaling. However, this view has changed dramatically in recent years with the recognition that certain SLs such as ceramide, sphingosine 1-phosphate and gangliosides, participate actively in signal transduction pathways, regulating many different cell functions such as proliferation, differentiation, adhesion and cell death. In particular, ceramide has attracted considerable attention in cell biology and biophysics due to its key role in the modulation of membrane physical properties, signaling and cell death regulation. This latter function is largely exerted by the ability of ceramide to activate the major pathways governing cell death such as the endoplasmic reticulum and mitochondria. Overall, the evidence so far indicates a key function of SLs in disease pathogenesis and hence their regulation may be of potential therapeutic relevance in different pathologies including liver diseases, neurodegeneration and cancer biology and therapy.
引用
收藏
页码:923 / 939
页数:17
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