Yang Z, Cao Z, Panjwani N
The New England Eye Center, Tufts University School of Medicine, Boston, Massachusetts 02111, USA.
Infect Immun. 1997 Feb;65(2):439-45. doi: 10.1128/iai.65.2.439-445.1997.
Acanthamoeba keratitis is a sight-threatening corneal infection. In a recent study, the saccharide mannose has been shown to inhibit the binding of Acanthamoeba organisms to the epithelium of the cornea (L. D. Morton, G. L. McLaughlin, and H. E. Whiteley, Infect. Immun. 59:3819-3822, 1991). In an attempt to determine the molecular mechanism by which acanthamoebae adhere to the surface of the cornea, the present study was designed to determine whether Acanthamoeba castellanii derived from an infected human cornea (i) binds to mannose-containing glycoproteins (mannose-GPs) of corneal epithelium and (ii) expresses one or more mannose-binding proteins. Mannose-GPs of primary cell cultures of rabbit corneal epithelium were isolated by using three different agarose-conjugated, mannose-specific lectins. By electrophoresis blot-overlay assays, 35S-labeled acanthamoebae were shown to bind to mannose-GPs of corneal epithelium and to a neoglycoprotein, mannose-bovine serum albumin (mannose-BSA). 35S-labeled acanthamoebae also bound to microtiter wells coated with mannose-BSA in a concentration-dependent manner. The binding of amoebae to mannose-GPs was blocked by free methyl-alpha-D-mannopyranoside. The parasites did not bind to galactose-BSA or to many other proteins lacking mannose residues. A membrane-associated mannose-binding protein (136 kDa) of A. castellanii was isolated by affinity chromatography of detergent extracts of unlabeled parasites and of cell surface biotin-labeled parasites on a p-aminophenyl alpha-D-mannopyranoside-agarose column. The affinity-purified protein of the amoeba was shown to bind specifically to mannose-BSA. In summary, a mannose-binding protein is present on the surface membranes of Acanthamoeba, and corneal epithelial cells express Acanthamoeba-reactive GPs. One of the mechanisms of Acanthamoeba adhesion to the corneal surface may involve interactions between the mannose-binding protein of Acanthamoeba and mannose-GPs on the surface of corneal epithelium.
棘阿米巴角膜炎是一种威胁视力的角膜感染。在最近的一项研究中,已证明糖类甘露糖可抑制棘阿米巴生物体与角膜上皮的结合(L.D.莫顿、G.L.麦克劳克林和H.E.怀特利,《感染与免疫》59:3819 - 3822,1991年)。为了确定棘阿米巴附着于角膜表面的分子机制,本研究旨在确定源自感染人类角膜的卡氏棘阿米巴是否(i)与角膜上皮含甘露糖的糖蛋白(甘露糖 - GP)结合,以及(ii)表达一种或多种甘露糖结合蛋白。通过使用三种不同的琼脂糖偶联的、甘露糖特异性凝集素,分离兔角膜上皮原代细胞培养物中的甘露糖 - GP。通过电泳印迹覆盖分析,显示35S标记的棘阿米巴与角膜上皮的甘露糖 - GP以及一种新糖蛋白甘露糖 - 牛血清白蛋白(甘露糖 - BSA)结合。35S标记的棘阿米巴也以浓度依赖的方式与包被有甘露糖 - BSA的微量滴定孔结合。阿米巴与甘露糖 - GP的结合被游离的α - D - 吡喃甘露糖苷阻断。这些寄生虫不与半乳糖 - BSA或许多其他缺乏甘露糖残基的蛋白质结合。通过在对氨基苯基α - D - 吡喃甘露糖苷 - 琼脂糖柱上对未标记寄生虫和细胞表面生物素标记寄生虫的去污剂提取物进行亲和层析,分离出卡氏棘阿米巴的一种膜相关甘露糖结合蛋白(136 kDa)。已证明阿米巴的亲和纯化蛋白特异性结合甘露糖 - BSA。总之,棘阿米巴的表面膜上存在一种甘露糖结合蛋白,并且角膜上皮细胞表达与棘阿米巴反应的GP。棘阿米巴附着于角膜表面的机制之一可能涉及棘阿米巴的甘露糖结合蛋白与角膜上皮表面的甘露糖 - GP之间的相互作用。