Bioactive sphingolipids in the modulation of the inflammatory response

被引:139
作者
El Alwani, Mazen
Wu, Bill Xingjun
Obeid, Lina M.
Hannun, Yusuf A.
机构
[1] Med Univ S Carolina, Dept Biochem & Mol Biol, Charleston, SC 29425 USA
[2] Dept Vet Affairs Med Ctr, Charleston, SC USA
[3] Med Univ S Carolina, Dept Med, Div Gen Internal Med, Charleston, SC 29425 USA
关键词
inflammation; ceramide; sphingosine; ceramide-1-phosphate; sphingosine-1-phosphate; cyclooxygenase; 2;
D O I
10.1016/j.pharmthera.2006.04.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Inflammation is viewed as a protective response against insults to the organism. It involves the recruitment of many cell types and the production of various inflammatory mediators in attempts to contain and reverse the insult. However, inflammation can lead to irreversible tissue destruction by itself and, therefore, can represent a disease state that causes significant morbidity and mortality. Understanding the molecular mechanisms controlling the inflammatory response is essential to formulate therapeutic strategies for the treatment of inflammatory conditions. In fact, substantial research has unveiled important aspects of the inflammatory machinery, both at the cellular and molecular levels. Recently, sphingolipids (SLs) have emerged as signaling molecules that regulate many cell functions, and ample evidence emphasizes their role in the regulation of inflammatory responses. Here, we review the role of bioactive SL as regulators and mediators of inflammatory responses. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:171 / 183
页数:13
相关论文
共 175 条
[1]   FARBERS DISEASE - A FINE-STRUCTURAL STUDY [J].
ABENOZA, P ;
SIBLEY, RK .
ULTRASTRUCTURAL PATHOLOGY, 1987, 11 (04) :397-403
[2]   Effects of cyclooxygenase-1 and-2 inhibition on gastric acid secretion and cardiovascular functions in rats [J].
Adami, M ;
Coppelli, G ;
Guaita, E ;
Pozzoli, C ;
Menozzi, A ;
Giovannini, E ;
Coruzzi, G .
PHARMACOLOGY, 2006, 76 (02) :84-92
[3]   Signalling pathways of the TNF superfamily: A double-edged sword [J].
Aggarwal, BB .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (09) :745-756
[4]   Formyl peptide receptor signaling in HL-60 cells through sphingosine kinase [J].
Alemany, R ;
Heringdorf, DMZ ;
van Koppen, CJ ;
Jakobs, KH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (07) :3994-3999
[5]   Mice deficient in sphingosine kinase 1 are rendered lymphopenic by FTY720 [J].
Allende, ML ;
Sasaki, T ;
Kawai, H ;
Olivera, A ;
Mi, YD ;
van Echten-Deckert, G ;
Hajdu, R ;
Rosenbach, M ;
Keohane, CA ;
Mandala, S ;
Spiegel, S ;
Proia, RL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (50) :52487-52492
[6]   Tumor necrosis factor receptor-associated factors (TRAFs) - a family of adaptor proteins that regulates life and death [J].
Arch, RH ;
Gedrich, RW ;
Thompson, CB .
GENES & DEVELOPMENT, 1998, 12 (18) :2821-2830
[7]   Physiologic role of interleukin-1 receptor antagonist [J].
Arend, WP ;
Gabay, C .
ARTHRITIS RESEARCH, 2000, 2 (04) :245-248
[8]   INTERLEUKIN-1 RECEPTOR ANTAGONIST [J].
AREND, WP .
ADVANCES IN IMMUNOLOGY, VOL 54, 1993, 54 :167-227
[9]   Ultraviolet A-induced modulation of Bcl-XL by p38 MAPK in human Keratinocytes -: Post-transcriptional regulation through the 3′-untranslated region [J].
Bachelor, MA ;
Bowden, GT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (41) :42658-42668
[10]  
BALLOU LR, 1992, J BIOL CHEM, V267, P20044