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疟疾环子孢子蛋白与肝细胞表面膜相关的硫酸乙酰肝素蛋白聚糖结合。

Malaria circumsporozoite protein binds to heparan sulfate proteoglycans associated with the surface membrane of hepatocytes.

作者信息

Frevert U, Sinnis P, Cerami C, Shreffler W, Takacs B, Nussenzweig V

机构信息

Michael Heidelberger Division of Immunology, Department of Pathology, Kaplan Cancer Center, NYU Medical Center, New York 10016.

出版信息

J Exp Med. 1993 May 1;177(5):1287-98. doi: 10.1084/jem.177.5.1287.

Abstract

During feeding by infected mosquitoes, malaria sporozoites are injected into the host's bloodstream and enter hepatocytes within minutes. The remarkable target cell specificity of this parasite may be explained by the presence of receptors for the region II-plus of the circumsporozoite protein (CS) on the basolateral domain of the plasma membrane of hepatocytes. We have now identified these receptors as heparan sulfate proteoglycans (HSPG). The binding of CS to the receptors is abolished by heparitinase treatment, indicating that the recognition of region II-plus is via the glycosaminoglycan chains. We have purified and partially characterized the CS-binding HSPGs from HepG2 cells. They have a molecular weight of 400,000-700,000, are tightly associated with the plasma membrane, and are released from the cell surface by very mild trypsinization, a property which the CS receptors share with the syndecan family of proteoglycans.

摘要

在受感染蚊子叮咬吸血时,疟原虫子孢子被注入宿主血液,并在数分钟内进入肝细胞。这种寄生虫显著的靶细胞特异性可能是由于肝细胞质膜基底外侧结构域存在环子孢子蛋白(CS)II区及其以上区域的受体。我们现已确定这些受体为硫酸乙酰肝素蛋白聚糖(HSPG)。用肝素酶处理可消除CS与受体的结合,这表明II区及其以上区域的识别是通过糖胺聚糖链进行的。我们已从HepG2细胞中纯化并部分鉴定了与CS结合的HSPG。它们的分子量为400,000 - 700,000,与质膜紧密结合,通过非常温和的胰蛋白酶处理可从细胞表面释放,CS受体与蛋白聚糖的syndecan家族具有这一共同特性。

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