Humbert C, Santisteban M S, Usson Y, Robert-Nicoud M
Equipe de Reconnaissance des Formes et Microscopie Quantitative, TIM3 Laboratory, USR CNRS 00690B, Joseph Fourier University, BP, Grenoble, France.
J Cell Sci. 1992 Sep;103 ( Pt 1):97-103. doi: 10.1242/jcs.103.1.97.
The intranuclear distribution of newly replicated DNA and of the proliferating cell nuclear antigen (PCNA) was mapped by confocal laser scanning microscopy after simultaneous immunofluorescent labelling of incorporated bromodeoxyuridine (BrdUrd) and PCNA. A mild hydrolysis with HCl followed by an enzymic digestion of DNA was used to produce single-stranded DNA required for BrdUrd immunorevelation, since this procedure preserves PCNA antigenicity. Optical sections obtained with a laser scanning microscope clearly showed a similar distribution of PCNA and BrdUrd within the nuclei, thus confirming previous observations on parallel labelled synchronized cultures. The intranuclear distribution of PCNA and BrdUrd varies concomitantly during the S phase of MCF-7 cells.
在对掺入的溴脱氧尿苷(BrdUrd)和增殖细胞核抗原(PCNA)进行同步免疫荧光标记后,通过共聚焦激光扫描显微镜绘制了新复制DNA和增殖细胞核抗原(PCNA)的核内分布。由于该程序可保留PCNA抗原性,因此先用HCl进行温和水解,然后对DNA进行酶消化,以产生BrdUrd免疫检测所需的单链DNA。用激光扫描显微镜获得的光学切片清楚地显示了PCNA和BrdUrd在细胞核内的相似分布,从而证实了先前对平行标记同步培养物的观察结果。在MCF-7细胞的S期,PCNA和BrdUrd的核内分布同时发生变化。