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细胞对损伤反应的修饰研究。II. 酸中毒对艾氏腹水瘤细胞缺氧损伤保护作用的电子显微镜研究。

Studies on the modification of the cellular response to injury. II. Electron microscopic studies on the protective effect of acidosis on anoxic injury of Ehrlich ascites tumor cells.

作者信息

Penttila A, Trump B F

出版信息

Virchows Arch B Cell Pathol. 1975;18(1):1-16. doi: 10.1007/BF02889230.

DOI:10.1007/BF02889230
PMID:238333
Abstract

Extracellular acidosis (ph 5.9 to 6.5) was found to be significantly retard the subcellular response of Ehrlich ascites tumor cells (EATC) to anoxic injury. The cells initially showed a reversible stage of cell injury with diffuse mitrochondrial condensation and swelling of endoplasmic reticulum (ER) at pH 7.9 by 1 h, while by 3 h at this pH all cells showed high amplitude and intramatrical flocculent densities of mitochondria, and fragmentation of membrane systems. At pH 7.4 cells were normal at 15 min., the mitochondria were condensed as above by 1 h, some cells still showed condensed mitochondria and dilated ER while others showed high amplitude swelling of mitochondria by 3 h and all cells showed irreversible changes by 4 h. At pH 5.9 to pH 6.5 mitochondria remained condensed until 3 h and only by 6 h did some cells show high amplitude swelling, whereas most cells showed persistent mitrochondrial condensation. Not until 8 h did all cells show high amplitude swelling of mitochondria. Furthermore, ultrastructural differences in the pattern of necrosis were seen at the lower pH values consisting of greater density of the cell sap, irregularly dispersed flocculent densities in apposition to fragmented cytoplasmic membranes and in mitochondria, and more prominent persistent clumping of nuclear chromatin.

摘要

研究发现,细胞外酸中毒(pH 5.9至6.5)会显著延缓艾氏腹水瘤细胞(EATC)对缺氧损伤的亚细胞反应。在pH 7.9时,细胞最初在1小时内表现出细胞损伤的可逆阶段,伴有弥漫性线粒体凝聚和内质网(ER)肿胀,而在此pH值下3小时时,所有细胞均表现出线粒体高振幅和基质内絮状密度增加,以及膜系统碎片化。在pH 7.4时,细胞在15分钟时正常,1小时时线粒体如上述那样凝聚,一些细胞在3小时时仍显示线粒体凝聚和内质网扩张,而另一些细胞则显示线粒体高振幅肿胀,所有细胞在4小时时均表现出不可逆变化。在pH 5.9至pH 6.5时,线粒体一直保持凝聚状态直至3小时,只有到6小时时一些细胞才显示出高振幅肿胀,而大多数细胞仍表现出线粒体持续凝聚。直到8小时所有细胞才显示出线粒体高振幅肿胀。此外,在较低pH值下可见坏死模式的超微结构差异,包括细胞液密度更高、与破碎的细胞质膜和线粒体并列的不规则分散的絮状密度,以及核染色质更明显的持续聚集。

相似文献

1
Studies on the modification of the cellular response to injury. II. Electron microscopic studies on the protective effect of acidosis on anoxic injury of Ehrlich ascites tumor cells.细胞对损伤反应的修饰研究。II. 酸中毒对艾氏腹水瘤细胞缺氧损伤保护作用的电子显微镜研究。
Virchows Arch B Cell Pathol. 1975;18(1):1-16. doi: 10.1007/BF02889230.
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Virchows Arch B Cell Pathol. 1975;18(1):17-34.
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Studies on cell surface conformation following injury. II. Scanning and transmission electron microscopy of cell surface changes following anoxic injury in Ehrlich ascites tumor cells.损伤后细胞表面构象的研究。II. 艾氏腹水瘤细胞缺氧损伤后细胞表面变化的扫描电镜和透射电镜观察
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引用本文的文献

1
Cell calcium, cell injury and cell death.细胞钙、细胞损伤与细胞死亡。
Environ Health Perspect. 1984 Aug;57:281-7. doi: 10.1289/ehp.8457281.
2
Organ culture of adult mouse intestine. I. Morphological results after 24 and 48 hours of culture.成年小鼠肠道的器官培养。I. 培养24小时和48小时后的形态学结果。
In Vitro. 1979 Apr;15(4):278-87. doi: 10.1007/BF02618952.
3
The transport and oxidation of succinate by Ehrlich ascites-tumour cells.艾氏腹水癌细胞对琥珀酸盐的转运与氧化作用
Biochem J. 1976 Oct 15;160(1):121-3. doi: 10.1042/bj1600121.