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用化学致癌物处理后细胞间连接的体外早期变化。

In vitro early changes in intercellular junctions by treatment with a chemical carcinogen.

作者信息

Tachikawa T, Kohno Y, Matsui Y, Yoshiki S

出版信息

Carcinogenesis. 1986 Jun;7(6):885-92. doi: 10.1093/carcin/7.6.885.

DOI:10.1093/carcin/7.6.885
PMID:3085968
Abstract

To examine early intercellular junction changes caused by treatment with 9,10-dimethyl-1,2-benzanthracene (DMBA), rat lingual epithelium was cultivated in isolation and observed by electrophysiological, freeze-fracture and whole-mount electron microscopy. Electrophysiological measurements showed a transient decrease in membrane potential of -10.2 mV 6 h after the treatment. It returned to almost the same level as that of the control group 1 day later. Six hours after treatment, input resistance decreased rapidly to 5.3 M omega but increased to 18.0 M omega 12 h after treatment. Transient reduction of input resistance and membrane potential occurred prior to the decrease in the coupling ratio 6 h after treatment with DMBA. In freeze-fracture replicas, the number of gap junctions decreased by approximately 45% of the control value 6 h after treatment with DMBA. At 12 h and thereafter, the number and area of gap junctions subsequently decreased by 60-80% of the control value. Alterations in the number and area of desmosomes were similar to those of the gap junctions. The formation of epithelial cytoskeletons, partially devoid of the 2-4 and 5-8 nm filaments was also observed. A decrease in the density of filament networks beneath the plasma membranes was especially apparent. Treatment with a carcinogen brought about morphological cellular changes as early as 6 h after treatment, and such early changes might trigger metabolic cellular abnormalities. Affected cells appear to move away from normal cells in a process of repeated destruction and revision of intercellular junctions, and cytoskeletons.

摘要

为研究9,10 - 二甲基 - 1,2 - 苯并蒽(DMBA)处理引起的早期细胞间连接变化,对大鼠舌上皮进行离体培养,并通过电生理学、冷冻蚀刻和整装电子显微镜观察。电生理学测量显示,处理后6小时膜电位短暂下降10.2 mV,1天后恢复到与对照组几乎相同的水平。处理后6小时,输入电阻迅速降至5.3 MΩ,但处理后12小时增加到18.0 MΩ。在用DMBA处理后6小时,输入电阻和膜电位的短暂降低先于偶联率的下降。在冷冻蚀刻复制品中,用DMBA处理6小时后,间隙连接的数量减少了约45%(相对于对照值)。在12小时及之后,间隙连接的数量和面积随后减少到对照值的60 - 80%。桥粒数量和面积的变化与间隙连接相似。还观察到上皮细胞骨架的形成,部分缺乏2 - 4和5 - 8纳米的细丝。质膜下细丝网络密度的降低尤为明显。用致癌物处理后6小时就出现了细胞形态学变化,这种早期变化可能引发细胞代谢异常。受影响的细胞似乎在细胞间连接和细胞骨架反复破坏和修复的过程中与正常细胞分离。

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The carcinogen benzo(e)pyrene is metabolized by DM15 cells without an uncoupling effect on their gap junctions.
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