Nagata Tetsuji
Department of Anatomy and Cell Biology, Shinshu University School of Medicine, Matsumoto, Japan.
Curr Radiopharm. 2012 Jan;5(1):5-14. doi: 10.2174/1874471011205010005.
For the purpose of studying the aging changes of macromolecular synthesis in the pancreatic acinar cells of experimental animals, we studied 10 groups of aging mice during development and aging from fetal day 19 to postnatal month 24. They were injected with 3H-uridine, a precursor for RNA synthesis, sacrificed and the pancreatic tissues were taken out, fixed and processed for light and electron microscopic radioautography. On many radioautograms the localization of silver grains demonstrating RNA synthesis in pancreatic acinar cells in respective aging groups were analyzed qualitatively. The number of mitochondria per cell, the number of labeled mitochondria with silver grains and the number of silver grains in each cell in respective aging groups were analyzed quantitatively in relation to the aging of animals. The results revealed that the RNA synthetic activity as expressed by the incorporations of RNA precursor, i.e., the number of silver grains in cell nuclei, cell organelles, changed due to the aging of animals. The number of mitochondria, the number of labeled mitochondria and the mitochondrial labeling index labeled with silver grains were counted in each pancreatic acinar cell. It was demonstrated that the number of mitochondria, the number of labeled mitochondria and the labeling indices showing RNA synthesis at various ages increased from embryonic day 19 to postnatal newborn day 1, 3, 9, 14, adult month 1, 2 and 6, reaching the maxima, then decreased to senile stage at postnatal year 1 to 2, indicating the aging changes. Based upon our findings, available literature on macromolecular synthesis in mitochondria of various cells are reviewed.
为了研究实验动物胰腺腺泡细胞中大分子合成的衰老变化,我们研究了10组从胚胎第19天到出生后24个月发育和衰老过程中的衰老小鼠。给它们注射RNA合成的前体3H-尿苷,然后处死,取出胰腺组织,固定并进行光镜和电镜放射自显影处理。在许多放射自显影片上,对各衰老组胰腺腺泡细胞中显示RNA合成的银粒定位进行了定性分析。对各衰老组中每个细胞的线粒体数量、带有银粒的标记线粒体数量以及每个细胞中的银粒数量与动物衰老的关系进行了定量分析。结果显示,由RNA前体掺入所表达的RNA合成活性,即细胞核、细胞器中的银粒数量,因动物衰老而发生变化。对每个胰腺腺泡细胞中的线粒体数量、标记线粒体数量以及用银粒标记的线粒体标记指数进行了计数。结果表明,从胚胎第19天到出生后第1天、第3天、第9天、第14天、成年第1个月、第2个月和第6个月,不同年龄段显示RNA合成的线粒体数量、标记线粒体数量和标记指数均增加,达到最大值,然后在出生后第1年到第2年下降到老年阶段,表明存在衰老变化。基于我们的研究结果,对各种细胞线粒体中大分子合成的现有文献进行了综述。