Nagata S, Umihira J, Nohara M, Amari F, Hanai T, Usuda N, Segawa K
Department of Ophthalmology, Shinshu University School of Medicine, Matsumoto, Japan.
Cell Mol Biol (Noisy-le-grand). 1995 Mar;41(2):313-8.
Ten normal human trabecular meshworks were examined by electron microscopy using avidin-biotin complex in order to investigate the localization of binding sites of eight lectins. The tissue specimens were fixed in paraformaldehyde and glutaraldehyde mixture and embedded in Lowicryl K4M at low temperature. The ultrathin sections were stained with biotin labelled lectins and colloidal gold labelled streptoavidin and were observed with the conventional transmission electron microscope. Some lectins such as ABA, ConA and DSA were localized on fine fibrils underneath the endothelium of the trabecular wall of the Schlemm's canal, electron-dense cores of elastic fibers, fine granular like materials, basement membranes, collagen fibers and the long-spacing fibers. However, the other lectins such as DBA, SBA, Lotus, UEA-I and RCA60 were not specifically localized in these tissues. From the results it was demonstrated that the differential ultrastructural localization of glycoconjugate residues in the human trabecular meshworks can be revealed using this lectin staining.
为了研究八种凝集素结合位点的定位,使用抗生物素蛋白-生物素复合物通过电子显微镜对十个正常人小梁网进行了检查。组织标本用多聚甲醛和戊二醛混合物固定,并在低温下包埋于Lowicryl K4M中。超薄切片用生物素标记的凝集素和胶体金标记的链霉抗生物素蛋白染色,并用传统透射电子显微镜观察。一些凝集素,如ABA、ConA和DSA,定位于施莱姆管小梁壁内皮下方的细纤维、弹性纤维的电子致密核心、细颗粒状物质、基底膜、胶原纤维和长间距纤维上。然而,其他凝集素,如DBA、SBA、莲凝集素、UEA-I和RCA60,在这些组织中没有特异性定位。从结果表明,使用这种凝集素染色可以揭示人小梁网中糖缀合物残基的超微结构差异定位。