Metabolism of sphingolipids in the gut and its relation to inflammation and cancer development

被引:162
作者
Duan, Rui-Dong [1 ]
Nilsson, Ake [2 ]
机构
[1] Lund Univ, Dept Clin Sci, Gastroenterol Lab, Biomed Ctr B11, S-22184 Lund, Sweden
[2] Univ Lund Hosp, Dept Clin Sci, Div Gastroenterol, S-22185 Lund, Sweden
基金
瑞典研究理事会;
关键词
Ceramide; Ceramidase; Ceramide kinase; Colon cancer; Glucosylceramide; Inflammatory bowel disease; Intestine; Sphingolipid; Sphingosine; Sphingosine kinase; Sphingosine-1-phosphatase; Sphingomyelin; Sphingomyelinase; INTESTINAL ALKALINE SPHINGOMYELINASE; LIPID PHOSPHATE PHOSPHATASES; SPHINGOSINE; 1-PHOSPHATE; COLON-CANCER; MOLECULAR-CLONING; EPITHELIAL-CELLS; GLUCOSYLCERAMIDE SYNTHASE; NEUTRAL CERAMIDASE; GLYCOSPHINGOLIPID COMPOSITION; ALPHA-GALACTOSYLCERAMIDE;
D O I
10.1016/j.plipres.2008.04.003
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 are abundant in the microvillar membrane of intestinal epithelial cells where they are essential for structural integrity and may act as receptors for toxins, virus and bacteria. Metabolism of dietary and membrane sphingolipids in the intestine generates ceramide, sphingosine, sphingosine-1-phosphate, and ceramide-1-phosphate, via the action of alkaline sphingomyelinase, neutral cerarmidase, sphingosine-l-kinase, and ceramide-l-kinase. These intermediary metabolites act as bioactive lipid messengers, influencing numerous cellular functions including growth, differentiation and apoptosis of both epithelial and immunocompetent cells in the gastrointestinal tract, and also the progress of inflammation and responsiveness of the mucosal cells to pathogens. This review summarizes background and recent progress in the metabolism of dietary and endogenous sphingolipids in the gut and its pathophysiological implications. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:62 / 72
页数:11
相关论文
共 180 条
  • [71] Familial adenomatous polyposis is associated with a marked decrease in alkaline sphingomyelinase activity:: a key factor to the unrestrained cell proliferation?
    Hertervig, E
    Nilsson, Å
    Björk, J
    Hultkrantz, R
    Duan, RD
    [J]. BRITISH JOURNAL OF CANCER, 1999, 81 (02) : 232 - 236
  • [72] HERTERVIG E, 2000, ALKALINE SPHINGOMYEL
  • [73] The way we view cellular (glyco)sphingolipids
    Hoetzl, Sandra
    Sprong, Hein
    van Meer, Gerrit
    [J]. JOURNAL OF NEUROCHEMISTRY, 2007, 103 : 3 - 13
  • [74] Lipid microdomains, lipid translocation and the organization of intracellular membrane transport (Review)
    Holthuis, JCM
    van Meer, G
    Huitema, K
    [J]. MOLECULAR MEMBRANE BIOLOGY, 2003, 20 (03) : 231 - 241
  • [75] Regulation of nuclear factor-κB in intestinal epithelial cells in a cell model of inflammation
    Homaidan, FR
    Chakroun, I
    El-Sabban, ME
    [J]. MEDIATORS OF INFLAMMATION, 2003, 12 (05) : 277 - 283
  • [76] Sphingosine-1-phosphate induces COX-2 expression via PI3K/Akt and p42/p44 MAPK pathways in rat vascular smooth muscle cells
    Hsieh, HL
    Wu, CB
    Sun, CC
    Liao, CH
    Lau, YT
    Yang, CM
    [J]. JOURNAL OF CELLULAR PHYSIOLOGY, 2006, 207 (03) : 757 - 766
  • [77] Identification of a family of animal sphingomyelin synthases
    Huitema, K
    van den Dikkenberg, J
    Brouwers, JFHM
    Holthuis, JCM
    [J]. EMBO JOURNAL, 2004, 23 (01) : 33 - 44
  • [78] A synthetic analog of α-galactosylceramide induces macrophage activation via the TLR4-signaling pathways
    Hung, Ling-Chien
    Lin, Chun-Cheng
    Hung, Shih-Kai
    Wu, Bing-Ching
    Jan, Mi-Dan
    Liou, Sheng-Hung
    Fu, Shu-Ling
    [J]. BIOCHEMICAL PHARMACOLOGY, 2007, 73 (12) : 1957 - 1970
  • [79] INHIBITION OF CHOLERA-TOXIN BY HUMAN-MILK FRACTIONS AND SIALYLLACTOSE
    IDOTA, T
    KAWAKAMI, H
    MURAKAMI, Y
    SUGAWARA, M
    [J]. BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1995, 59 (03) : 417 - 419
  • [80] Inhibitory effect of dietary monoglucosylceramide 1-O-β-glucosyl-N-2′-hydroxyarachidoyl-4,8-sphingadienine on two different categories of colon preneoplastic lesions induced by 1,2-dimethylhydrazine in F344 rats
    Inamine, M
    Suzui, M
    Morioka, T
    Kinjo, T
    Kaneshiro, T
    Sugishita, T
    Okada, T
    Yoshimi, N
    [J]. CANCER SCIENCE, 2005, 96 (12): : 876 - 881