Ceramide and other sphingolipids in cellular responses

被引:86
作者
Yang, J
Yu, YN
Sun, SY
Duerksen-Hughes, PJ [1 ]
机构
[1] Loma Linda Univ, Sch Med, Ctr Mol Biol & Gene Therapy, Dept Biochem & Microbiol, Loma Linda, CA 92350 USA
[2] Zhejiang Univ, Sch Med, Dept Pathol & Pathophysiol, Hangzhou 310027, Zhejiang, Peoples R China
[3] Zhejiang Univ, Sch Med, Dept Publ Hlth, Hangzhou 310027, Zhejiang, Peoples R China
[4] Shandong Univ, Affiliated Hosp, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
sphingolipids; ceramide; stress response; growth control; apoptosis;
D O I
10.1385/CBB:40:3:323
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Formerly considered to serve only as structural components, sphingolipids are emerging as an important group of signaling molecules involved in many cellular events, including cell growth, senescence, meiotic maturation, and cell death. They are also implicated in functions such as inflammation and the responses to heat shock and genotoxic stress. Defects in the metabolism of sphingolipids are related to various genetic disorders, and sphingolipids have the potential to serve as therapeutic agents for human diseases such as colon cancer and viral or bacterial infections. The best-studied member of this family, ceramide, which also serves as the structural backbone for other sphingolipids, is an important mediator in multiple cellular signaling pathways. The metabolism and functions of sphingolipids are discussed in this review, with a focus on ceramide regulation in various cellular responses.
引用
收藏
页码:323 / 350
页数:28
相关论文
共 255 条
[1]
Sphingolipids as biomarkers of fumonisin exposure and risk of esophageal squamous cell carcinoma in China [J].
Abnet, CC ;
Borkowf, CB ;
Qiao, YL ;
Albert, PS ;
Wang, E ;
Merrill, AH ;
Mark, SD ;
Dong, ZW ;
Taylor, PR ;
Dawsey, SM .
CANCER CAUSES & CONTROL, 2001, 12 (09) :821-828
[2]
Cell-permeable ceramides prevent the activation of phospholipase D by ADP-ribosylation factor and RhoA [J].
Abousalham, A ;
Liossis, C ;
OBrien, L ;
Brindley, DN .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (02) :1069-1075
[3]
Sphingoid bases and ceramide induce apoptosis in HT-29 and HCT-116 human colon cancer cells [J].
Ahn, EH ;
Schroeder, JJ .
EXPERIMENTAL BIOLOGY AND MEDICINE, 2002, 227 (05) :345-353
[4]
Influence of Bcl-2 overexpression on the ceramide pathway in daunorubicin-induced apoptosis of leukemic cells [J].
Allouche, M ;
Bettaieb, A ;
Vindis, C ;
Rousse, A ;
Grignon, C ;
Laurent, G .
ONCOGENE, 1997, 14 (15) :1837-1845
[5]
Sphingosine 1-phosphate-induced cell proliferation, survival, and related signaling events mediated by G protein-coupled receptors Edg3 and Edg5 [J].
An, SZ ;
Zheng, YH ;
Bleu, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (01) :288-296
[6]
Synthesis and biochemical investigation of scyphostatin analogues as inhibitors of neutral sphingomyelinase [J].
Arenz, C ;
Gartner, M ;
Wascholowski, V ;
Giannis, A .
BIOORGANIC & MEDICINAL CHEMISTRY, 2001, 9 (11) :2901-2904
[7]
Sphingomyelin metabolites in vascular cell signaling and atherogenesis [J].
Augé, N ;
Nègre-Salvayre, A ;
Salvayre, R ;
Levade, T .
PROGRESS IN LIPID RESEARCH, 2000, 39 (03) :207-229
[8]
BALLOU LR, 1997, SPHINGOLIPID MEDIATE
[9]
BAD enables ceramide to signal apoptosis via Ras and Raf-1 [J].
Basu, S ;
Bayoumy, S ;
Zhang, Y ;
Lozano, J ;
Kolesnick, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (46) :30419-30426
[10]
Sphingolipids and the regulation of the immune response [J].
Baumruker, T ;
Prieschl, EE .
SEMINARS IN IMMUNOLOGY, 2002, 14 (01) :57-63