The control of the balance between ceramide and sphingosine-1-phosphate by sphingosine kinase: Oxidative stress and the seesaw of cell survival and death

被引:198
作者
Van Brocklyn, James R. [1 ]
Williams, Joseph B. [1 ]
机构
[1] Ohio State Univ, Dept Evolut Ecol & Organismal Biol, Columbus, OH 43210 USA
来源
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY | 2012年 / 163卷 / 01期
基金
美国国家科学基金会;
关键词
Sphingolipids; Apoptosis; Autophagy; Senescence; Aging; MYELOID-LEUKEMIA CELLS; ISCHEMIA-REPERFUSION INJURY; IMATINIB-INDUCED APOPTOSIS; ANTICANCER DRUG CISPLATIN; PROTEIN-COUPLED RECEPTORS; BREAST-CANCER CELLS; ELEGANS LIFE-SPAN; SACCHAROMYCES-CEREVISIAE; DICTYOSTELIUM-DISCOIDEUM; SPHINGOLIPID METABOLISM;
D O I
10.1016/j.cbpb.2012.05.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Sphingolipids are components of all eukaryotic cells that play important roles in a wide variety of biological processes. Ceramides and sphingosine-1-phosphate (S1P) are signaling molecules that regulate cell fate decisions in a wide array of species including yeast, plants, vertebrates, and invertebrates. Ceramides favor anti-proliferative and cell death pathways such as senescence and apoptosis, whereas S1P stimulates cell proliferation and survival pathways. The control of cell fate by these two interconvertible lipids has been called the sphingolipid rheostat or sphingolipid biostat. Sphingosine kinase, the enzyme that synthesizes SIP, is a crucial enzyme in regulation of the balance of these sphingolipids. Sphingosine kinase has been shown to play dynamic roles in the responses of cells to stress, leading to modulation of cell fate through a variety of signaling pathways impinging on the processes of cell proliferation, apoptosis, autophagy and senescence. This review summarizes the roles of sphingosine kinase signaling in these processes and the mechanisms mediating these responses. In addition, we discuss the evidence tying sphingosine kinase-mediated stress responses to the process of aging. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:26 / 36
页数:11
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