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10.1155/2015/120748

http://scihub22266oqcxt.onion/10.1155/2015/120748
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suck abstract from ncbi


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pmid26609196
      Mediators+Inflamm 2015 ; 2015 (ä): 120748
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  • Role of Ceramide from Glycosphingolipids and Its Metabolites in Immunological and Inflammatory Responses in Humans #MMPMID26609196
  • Iwabuchi K ; Nakayama H ; Oizumi A ; Suga Y ; Ogawa H ; Takamori K
  • Mediators Inflamm 2015[]; 2015 (ä): 120748 PMID26609196 show ga
  • Glycosphingolipids (GSLs) are composed of hydrophobic ceramide and hydrophilic sugar chains. GSLs cluster to form membrane microdomains (lipid rafts) on plasma membranes, along with several kinds of transducer molecules, including Src family kinases and small G proteins. However, GSL-mediated biological functions remain unclear. Lactosylceramide (LacCer, CDw17) is highly expressed on the plasma membranes of human phagocytes and mediates several immunological and inflammatory reactions, including phagocytosis, chemotaxis, and superoxide generation. LacCer forms membrane microdomains with the Src family tyrosine kinase Lyn and the G?i subunit of heterotrimeric G proteins. The very long fatty acids C24:0 and C24:1 are the main ceramide components of LacCer in neutrophil plasma membranes and are directly connected with the fatty acids of Lyn and G?i. These observations suggest that the very long fatty acid chains of ceramide are critical for GSL-mediated outside-in signaling. Sphingosine is another component of ceramide, with the hydrolysis of ceramide by ceramidase producing sphingosine and fatty acids. Sphingosine is phosphorylated by sphingosine kinase to sphingosine-1-phosphate, which is involved in a wide range of cellular functions, including growth, differentiation, survival, chemotaxis, angiogenesis, and embryogenesis, in various types of cells. This review describes the role of ceramide moiety of GSLs and its metabolites in immunological and inflammatory reactions in human.
  • |Ceramides/*physiology [MESH]
  • |Glycosphingolipids/*physiology [MESH]
  • |Humans [MESH]
  • |Inflammation/*etiology [MESH]
  • |Keratinocytes/immunology [MESH]
  • |Lysophospholipids/physiology [MESH]
  • |Membrane Microdomains/chemistry [MESH]
  • |Signal Transduction [MESH]


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