Ulrich R G, McClung J K
J Ultrastruct Res. 1983 Mar;82(3):327-34. doi: 10.1016/s0022-5320(83)80020-3.
The process of chicken erythrocyte-mediated microinjection of cultured BHK cells was studied by correlative secondary and backscattered electron imaging. The intense staining of the chicken erythrocyte nucleus by uranyl acetate was found to produce a backscattered electron signal sufficient to follow its position during cell fusion and microinjection. Initially, the erythrocyte ghosts were found to bind to the target cell surfaces. The microinjection process was complete within 2 to 4 hr, as evidenced by the presence of the erythrocyte nucleus within the cytoplasm of the target cell. By 24 hr, the internalized erythrocyte nuclei were difficult to distinguish by backscattered electron imaging. Some erythrocyte ghosts entered the cells intact by some method other than cell fusion, presumably phagocytosis.
通过相关的二次电子成像和背散射电子成像研究了鸡红细胞介导的培养BHK细胞显微注射过程。发现醋酸铀对鸡红细胞核的强烈染色产生了足以在细胞融合和显微注射过程中追踪其位置的背散射电子信号。最初,发现红细胞空壳与靶细胞表面结合。显微注射过程在2至4小时内完成,靶细胞胞质中存在红细胞核证明了这一点。到24小时时,内化的红细胞核通过背散射电子成像难以区分。一些红细胞空壳通过细胞融合以外的某种方法完整地进入细胞,推测是吞噬作用。