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作 者:Hongyan Kang Jinyan Lu Jiali Yang Yubo Fan Xiaoyan Deng
机构地区:[1]Key Laboratory for Biomechanics and Mechanobiology of Ministry of Education,School of Biological Science and Medical Engineering,Beihang University,Beijing,100083,China [2]Beijing Advanced Innovation Centre for Biomedical Engineering,Beihang University,Beijing,100083,China
出 处:《Medicine in Novel Technology and Devices》2019年第3期1-8,共8页医学中新技术与新装备(英文)
基 金:supported by Grants-in-Aid from the National Natural Science Foundation of China(No.31870940,11772036,11572028,11421202);National Key Research and Development Program in China(No.2017YFB0702501);the Fundamental Research Funds for the Central Universities.
摘 要:Although atherosclerosis is a multifactorial process,proteoglycans mediated lipoprotein(LDL)retention at the subendothelial space is a necessary and sufficient event in provoking lesion initiation.Proteoglycans(PGs)are usually composed of one core protein backbone with one or more glycosaminoglycan chains(GAGs)covalently linked,mainly include perlecan,biglycan,versican,and decorin.The interaction between LDL and proteoglycans is apparently mediated by the basic amino acids in apoB-100,the moiety of LDL,electrostatic interacting with the negatively charged GAGs(sulfate or carbohydrate groups)of proteoglycans or though some bridge molecules like sphingomyelinase(SMase)or lipoprotein lipase(LpL).In the later section,we collate the promising therapeutic approaches that have been proposed up to now,targeting LDL-PGs interaction.It should be concluded that previous studies on interaction between LDL and PGs mainly focused on perlecan,biglycan,decorin,and versican that all located in the extracellular matrix(ECM),future studies should pay more attention to the endothelial surface glycocalyx and its interaction with LDLs,seeking promising therapeutic targets more specifically.
关 键 词:PROTEOGLYCANS Low-density lipoprotein ATHEROSCLEROSIS Endothelial glycocalyx
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