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关于硫酸化多糖在体外抑制HIV感染机制的研究。

Investigations into the mechanism by which sulfated polysaccharides inhibit HIV infection in vitro.

作者信息

McClure M O, Moore J P, Blanc D F, Scotting P, Cook G M, Keynes R J, Weber J N, Davies D, Weiss R A

机构信息

Chester Beatty Laboratories, Institute of Cancer Research, London, England.

出版信息

AIDS Res Hum Retroviruses. 1992 Jan;8(1):19-26. doi: 10.1089/aid.1992.8.19.

Abstract

Sulfated polysaccharides have been shown to inhibit human immunodeficiency virus (HIV) infection in vitro. Dextrin sulfate, fucoidan, and dextran sulfate fail to neutralize virions directly, but interact with target cells to inhibit virus entry. Ionic interactions of sulfated polyanions with oppositely charged cell surface components, including CD4, have been assumed to be the inhibitory mechanism. It is shown that the sulfated polysaccharides inhibit infection of both CD4+ and CD4- cell lines by HIV and also that they inhibit HTLV-1 and, to a lesser extent, the simian retrovirus, MPMV, which use receptors other than CD4. One binding site for radiolabeled fucoidan on the surface of human T cells is an 18 kD protein, but its significance is not yet clear.

摘要

硫酸化多糖已被证明在体外可抑制人类免疫缺陷病毒(HIV)感染。硫酸糊精、岩藻依聚糖和硫酸葡聚糖不能直接中和病毒粒子,但可与靶细胞相互作用以抑制病毒进入。硫酸化聚阴离子与带相反电荷的细胞表面成分(包括CD4)的离子相互作用被认为是其抑制机制。研究表明,硫酸化多糖可抑制HIV对CD4+和CD4-细胞系的感染,还可抑制人类嗜T淋巴细胞病毒1型(HTLV-1),并在较小程度上抑制猿猴逆转录病毒MPMV,后者使用CD4以外的受体。放射性标记的岩藻依聚糖在人T细胞表面的一个结合位点是一种18 kD的蛋白质,但其意义尚不清楚。

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