de Farias P M Albuquerque, Santos B Saegesser, de Menezes F Duarte, Ferreira R de Carvalho, Barjas-Castro M de Lourdes, Castro V, Lima P R Moura, Fontes A, Cesar C L
Departamento de Biofísica e Radiobiologia - CCB, Federal University of Pernambuco, Cid. Universitária CEP 50670-901 Recife-PE, Brazil.
J Microsc. 2005 Sep;219(Pt 3):103-8. doi: 10.1111/j.1365-2818.2005.01501.x.
We report a new and efficient methodology of labelling red blood cells, in order to investigate the expression of anti-A antigen, employing luminescent semiconductor nanocrystals. Highly luminescent and stable core-shell cadmium sulphide/cadmium hydroxide [CdS/CdS(OH)2] colloidal particles were obtained in the nanometre size range. The surface of these particles was characterized by using a monoclonal anti-A antibody via a one-step glutaraldehyde cross-linking procedure, followed by conjugation of the particles to red cells of blood groups A+, and O+. Laser scanning confocal microscopy images indicated that after conjugation for 30 min, A+ and erythrocytes presented different patterns of dual bright emission whereas the O+ group cells showed no emission. We suggest that this labelling procedure may be applied as a quantitative tool to investigate the distribution and expression of alloantigen in red blood cells.
我们报告了一种标记红细胞的新型高效方法,以便利用发光半导体纳米晶体研究抗A抗原的表达。在纳米尺寸范围内获得了高发光且稳定的核壳硫化镉/氢氧化镉[CdS/CdS(OH)2]胶体颗粒。通过一步戊二醛交联程序,使用单克隆抗A抗体对这些颗粒的表面进行了表征,随后将颗粒与A+和O+血型的红细胞结合。激光扫描共聚焦显微镜图像表明,结合30分钟后,A+红细胞呈现出不同的双亮发射模式,而O+组细胞则无发射。我们认为这种标记程序可作为一种定量工具,用于研究红细胞中同种异体抗原的分布和表达。