Bennett F C, Busch H, Lischwe M A, Yeoman L C
J Cell Biol. 1983 Nov;97(5 Pt 1):1566-72. doi: 10.1083/jcb.97.5.1566.
To determine whether red blood cell-mediated microinjection of antibodies can be used to study nuclear protein localization and function, we microinjected antibodies that have been shown to react specifically with nucleolar acidic phosphoprotein C23 into Walker 256 cells. The intracellular distribution of microinjected anti-C23 antibodies and preimmune immunoglobulins were determined by immunofluorescence. At 3 h after microinjection, affinity-purified anti-C23 antibodies were localized in the cytoplasm and nucleolus. At 17 h after microinjection, the affinity-purified antibody was localized to those nucleolar structures previously shown to contain protein C23. Furthermore, the antibody remained localized in the nucleolus for at least 36 h after microinjection. In contrast to the results obtained with specific antibodies, preimmune immunoglobulins remained in the cytoplasm 36 h after microinjection. These results indicate that red blood cell-mediated microinjection of antibodies can be used to study nucleolar and nuclear antigens.
为了确定红细胞介导的抗体显微注射是否可用于研究核蛋白的定位和功能,我们将已证明能与核仁酸性磷酸蛋白C23特异性反应的抗体显微注射到Walker 256细胞中。通过免疫荧光确定显微注射的抗C23抗体和免疫前免疫球蛋白的细胞内分布。显微注射后3小时,亲和纯化的抗C23抗体定位于细胞质和核仁。显微注射后17小时,亲和纯化的抗体定位于先前显示含有蛋白C23的那些核仁结构。此外,显微注射后抗体至少在核仁中保持36小时。与使用特异性抗体获得的结果相反,免疫前免疫球蛋白在显微注射后36小时仍留在细胞质中。这些结果表明红细胞介导的抗体显微注射可用于研究核仁和核抗原。