人表皮生长因子对原代培养新生大鼠肝细胞胆管发育的影响。

Y Kohno, M Fukunaga, K Shiraki, H Akiyoshi
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引用次数: 1

摘要

我们研究了人表皮生长因子(hEGF)对原代培养的新生儿肝细胞的细胞骨架结构和细胞间接触的影响,hEGF是肝细胞的生长促进因子。采用新开发的扫描电镜技术对培养肝细胞的细胞接触和胆管(BC)的超微结构特征进行了观察。与对照组相比,hEGF加胰岛素孵育3 h的新生肝细胞形状变化更大,细胞接触非常松散,有许多长纤维。此时,微管或微丝的分布没有变化。hEGF加胰岛素作用21 h后,微丝的分布发生改变。肌动蛋白丝不再包围BC,但在细胞周围观察到;此外,DNA合成率提高到对照组的3.9倍。地塞米松治疗3 h后,细胞直接接触紧密,21 h后,微扩张的BC周围出现肌动蛋白丝,但DNA合成没有增加。透射电镜显示,hEGF作用3 h后,BC中辣根过氧化物酶的转运和分泌受到抑制。这些结果表明,hEGF首先影响肝细胞极性形成所必需的细胞接触,然后影响肌动蛋白丝的分布,抑制功能性BC的发育。
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Effects of human epidermal growth factor on the development of bile canaliculi in neonatal rat hepatocytes in primary culture.

We have examined the effects of human epidermal growth factor (hEGF), a growth-promoting factor for hepatocytes, on the cytoskeletal structure and intercellular contacts in neonatal hepatocytes in primary culture. The ultrastructural characteristics of cellular contacts and bile canaliculi (BC) were examined using a newly developed technique of scanning electron microscopy for cultured hepatocytes. The neonatal hepatocytes incubated with hEGF plus insulin for 3 h showed more variety in shape than controls, and their cellular contacts were very loose with many long fibers. At this time, there were no changes in the distribution of microtubules or microfilaments. After treatment with hEGF plus insulin for 21 h, the distribution of microfilaments was altered. Actin filaments no longer surrounded BC, but were observed near the cell periphery; in addition, DNA synthesis was increased to 3.9 times the rate in controls. Treatment with dexamethasone for 3 h caused tight straight cellular contacts, and after 21 h actin filaments appeared around slightly dilated BC, but there was no increase in DNA synthesis. Transmission electron microscopy showed that the transport and secretion of horseradish peroxidase in BC was inhibited after 3-h incubation with hEGF. These results suggested that hEGF first affected the cellular contacts of hepatocytes necessary for the development of cellular polarity, and then affected the distribution of actin filaments, the development of functioning BC being suppressed.

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