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生命周期过程中人类肝细胞多倍体化动力学

Human hepatocyte polyploidization kinetics in the course of life cycle.

作者信息

Kudryavtsev B N, Kudryavtseva M V, Sakuta G A, Stein G I

机构信息

Institute of Cytology, Russian Academy of Sciences, St-Petersburg.

出版信息

Virchows Arch B Cell Pathol Incl Mol Pathol. 1993;64(6):387-93. doi: 10.1007/BF02915139.

DOI:10.1007/BF02915139
PMID:8148960
Abstract

The processes of polyploidization in normal human liver parenchyma from 155 individuals aged between 1 day and 92 years were investigated by Feulgen-DNA cytophotometry. It was shown that polyploid hepatocytes appear in individuals from 1 to 5 years old. Up to the age of 50 years the accumulation rate of binucleate and polyploid cells is very slow, but subsequently hepatocyte polyploidization is intensified, and in patients aged 86-92 years the relative number of cells with polyploid nuclei is about 27%. Only a few hepatocytes in the normal human liver reach 16C and 8C x 2 ploidy levels for mononucleate and binucleate cells respectively. Using a mathematical modeling method, it was shown that during postnatal liver growth the polyploidization process in human liver is similar to that in the rat, and that polyploid cells are formed mainly from binucleate cells. As in rats, prior to an increase in ploidy level, diploid human hepatocytes can pass several times through the usual mitotic cycles maintaining their initial ploidy level. After birth, only one in ten hepatocytes starting DNA synthesis enters the polyploidization process. At maturity about 60% of 2C-hepatocytes starting DNA synthesis divide by conventional mitosis, the rest dividing by acytokinetic mitosis leading to the formation of binucleate cells. During ageing the probability of hepatocyte polyploidization increases and in this period there are two polyploid or binucleate cells for every diploid dividing by conventional mitosis.

摘要

采用福尔根 DNA 细胞光度法研究了 155 名年龄在 1 天至 92 岁之间的正常人肝实质中的多倍体化过程。结果表明,多倍体肝细胞出现在 1 至 5 岁的个体中。在 50 岁之前,双核和多倍体细胞的积累速度非常缓慢,但随后肝细胞多倍体化加剧,在 86 - 92 岁的患者中,多倍体核细胞的相对数量约为 27%。在正常人类肝脏中,只有少数肝细胞分别达到单核细胞的 16C 和双核细胞的 8C×2 倍体水平。使用数学建模方法表明,在出生后肝脏生长过程中,人类肝脏中的多倍体化过程与大鼠相似,多倍体细胞主要由双核细胞形成。与大鼠一样,在倍性水平增加之前,二倍体人类肝细胞可以多次通过正常的有丝分裂周期,保持其初始倍性水平。出生后,开始 DNA 合成的肝细胞中只有十分之一进入多倍体化过程。在成熟时,开始 DNA 合成的 2C 肝细胞中约 60%通过常规有丝分裂分裂,其余的通过无胞质有丝分裂分裂,导致双核细胞的形成。在衰老过程中,肝细胞多倍体化的概率增加,在此期间,每一个通过常规有丝分裂分裂的二倍体细胞会产生两个多倍体或双核细胞。

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