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首页> 外文期刊>Organic & biomolecular chemistry >Cholesteryl 6-O-acyl-α-glucosides from diverse Helicobacter spp. signal through the C-type lectin receptor Mincle
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Cholesteryl 6-O-acyl-α-glucosides from diverse Helicobacter spp. signal through the C-type lectin receptor Mincle

机译:来自不同幽门螺杆菌的胆固醇6-O-酰基-α-葡糖苷。信号通过C型凝集素受体MINCL

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摘要

Helicobacter spp. are Gram-negative bacteria that cause a spectrum of disease in the gut, biliary tree and liver. Many Helicobacter spp. produce a range of cholesteryl α-glucosides that have the potential to act as pathogen associated molecular patterns. We report a highly stereoselective α-glucosylation of cholesterol using 3,4,6-tri-O-acetyl-2-O-benzyl-D-glucopyranosyl N-phenyl-2,2,2-trifluoroacetimidate, which allowed the synthesis of cholesteryl α-glucoside (αCG) and representative Helicobacter spp. cholesteryl 6-O-acyl-α-glucosides (αCAGs; acyl = C12:0, 14:0, C16:0, C18:0, C18:1). All αCAGs, irrespective of the nature of their acyl chain composition, strongly agonised signalling through the C-type lectin receptor Mincle from human and mouse to similar degrees. By contrast, aCG only weakly signalled through human Mincle, and did not signal through mouse Mincle. These results provide a molecular basis for understanding of the immunobiology of non-pylori Helicobacter infections in humans and other animals.
机译:Helicobacter SPP。是革兰阴性细菌,导致肠道,胆汁树和肝脏的疾病。许多幽门螺杆菌spp。产生一系列胆囊炎α-葡糖苷,其具有充当病原体相关的分子模式。我们通过3,4,6-三-4-乙酰基-2-o-苄基-d-吡喃葡萄糖烯基N-苯基-2,2,2,2-三氟丙依附物培养了胆固醇的高度立体化α-葡糖基化,允许合成胆固醇α-葡糖苷(αcg)和代表性螺旋菌SPP。胆固醇6-O-酰基-α-葡糖苷(αcags; acyl = C12:0,14:0,C16:0,C18:0,C18:1)。所有αcags,无论其酰基链组合物的性质如何,通过从人和小鼠到类似程度的C型凝集素受体Mincle强烈痛苦的信号传导。相比之下,ACG只能通过人类MINCL弱发信号,并没有通过鼠标即可发出信号。这些结果为了解人类和其他动物的非幽门螺杆菌感染免疫学的理解分子基础。

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  • 来源
    《Organic & biomolecular chemistry 》 |2020年第39期| 7907-7915| 共9页
  • 作者单位

    School of Chemistry and Bio21 Molecular Science and Biotechnology Institute University of Melbourne Parkville Victoria 3010 Australia;

    Department of Molecular Immunology Immunology Frontier Research Center Osaka University Suita 565-0871 Japan Department of Molecular Immunology Research Institute for Microbial Diseases Osaka University Suita 565-0871 Japan;

    Department of Molecular Immunology Immunology Frontier Research Center Osaka University Suita 565-0871 Japan Department of Molecular Immunology Research Institute for Microbial Diseases Osaka University Suita 565-0871 Japan;

    School of Chemistry and Bio21 Molecular Science and Biotechnology Institute University of Melbourne Parkville Victoria 3010 Australia;

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