Olea M T, Nagata T
Department of Anatomy and Cell Biology, Shinshu University, School of Medicine, Matsumoto, Japan.
Cell Mol Biol. 1992 Apr;38(2):115-22.
Simultaneous localization of 3H-thymidine incorporation and acid phosphatase (AcP) activity was undertaken by combined radioautography and cytochemistry in the spleen of mice at different ages. The localization of radiolabelled thymidine was used to determine the site of DNA synthesis (cell proliferation), while AcP activity as a marker for cell lysis/death. For EM radioautography (EMRAG), the tissue sections were incubated in a medium containing 3H-thymidine and processed for radioautography, while the lanthanide-based method for the ultrastructural localization of AcP activity was employed. Quantitation of AcP activity was carried out by X-ray microanalysis. In all tissue sections examined, mostly of the labelled nuclei were observed in the hematopoietic cells. Few mitochondria of these cells were labelled. The labeling index was expressed as the percentage of labelled cells over the total number of counted cells. The labeling indices dropped considerably from day one after birth and progressively until the 10th month. The result of AcP activity correlated well with the result of a previous work (Olea, 1991). The localization of radiolabelled thymidine and AcP activity were not hindered by the simultaneous exposure of the same tissue section to 3H-thymidine and AcP cytochemical media. Interestingly enough, the spleen actively participates both in hematopoiesis and erythrophagocytosis. Prominently, it is most active during the early postnatal life. However, their influence declined considerably at the later stage of life (adult stage).
通过放射自显影术和细胞化学相结合的方法,对不同年龄小鼠脾脏中3H-胸腺嘧啶核苷掺入和酸性磷酸酶(AcP)活性进行了同步定位。利用放射性标记胸腺嘧啶核苷的定位来确定DNA合成(细胞增殖)的部位,而AcP活性作为细胞裂解/死亡的标志物。对于电子显微镜放射自显影术(EMRAG),将组织切片在含有3H-胸腺嘧啶核苷的培养基中孵育并进行放射自显影处理,同时采用基于镧系元素的方法对AcP活性进行超微结构定位。通过X射线微分析对AcP活性进行定量。在所有检查的组织切片中,大部分标记的细胞核见于造血细胞。这些细胞中很少有线粒体被标记。标记指数表示为标记细胞数占计数细胞总数的百分比。标记指数从出生后第一天开始显著下降,并持续下降直至第10个月。AcP活性的结果与先前一项研究(Olea,1991年)的结果相关性良好。同一组织切片同时暴露于3H-胸腺嘧啶核苷和AcP细胞化学培养基中,并不妨碍放射性标记胸腺嘧啶核苷和AcP活性的定位。有趣的是,脾脏积极参与造血和红细胞吞噬作用。显著的是,它在出生后早期最为活跃。然而,它们的影响在生命后期(成年期)显著下降。