致病性卡伯氏棘阿米巴诱导大鼠小胶质细胞病变:形态学和细胞因子释放

Ho-Joon Shin, M. Cho, Suk-Yul Jung, Hyung-Il Kim, Sun Park, J. Seo, Jung-Chil Yoo, K. Im
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引用次数: 31

摘要

为了确定致病性库伯氏棘阿米巴滋养体和裂解物是否能诱导原代培养的小胶质细胞发生细胞病变,采用透射电镜(TEM)观察细胞形态学变化。此外,还观察了小胶质细胞分泌肿瘤坏死因子α (TNF-α)和白细胞介素-1β (IL-1β)两种细胞因子。致病性culbertsoni的滋养体与小胶质细胞接触并产生足趾。透射电镜显示,与阿米巴滋养体共培养的小胶质细胞经历了坏死过程,并伴有细胞膜的裂解。与阿米巴裂解液共培养的小胶质细胞透射电镜显示,细胞质小液泡的膜和细胞膜被裂解。小胶质细胞与库氏梭菌滋养体或裂解物共培养6 h时,TNF-α的分泌量增加。与库伯氏单胞菌共培养的小胶质细胞在培养6 h时分泌的IL-1β量与对照组相近,但与库伯氏单胞菌裂解液共培养时分泌的IL-1β量减少。上述结果提示,致病性卡伯梭菌可诱导原代培养大鼠小胶质细胞的细胞病变,其特点是小胶质细胞坏死,小胶质细胞分泌TNF-α和IL-1β水平发生变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytopathic Changes in Rat Microglial Cells Induced by Pathogenic Acanthamoeba culbertsoni: Morphology and Cytokine Release
ABSTRACT To determine whether pathogenic Acanthamoeba culbertsoni trophozoites and lysate can induce cytopathic changes in primary-culture microglial cells, morphological changes were observed by transmission electron microscopy (TEM). In addition, the secretion of two kinds of cytokines, tumor necrosis factor alpha (TNF-α) and interleukin-1β (IL-1β), from microglial cells was observed. Trophozoites of pathogenic A. culbertsoni made contact with microglial cells and produced digipodia. TEM revealed that microglial cells cocultured with amoebic trophozoites underwent a necrotic process, accompanied by lysis of the cell membrane. TEM of microglial cells cocultured with amoebic lysate showed that the membranes of the small cytoplasmic vacuoles as well as the cell membrane were lysed. The amounts of TNF-α secreted from microglial cells cocultured with A. culbertsoni trophozoites or lysate increased at 6 h of incubation. The amounts of IL-1β secreted from microglial cells cocultured with A. culbertsonitrophozoites at 6 h of incubation was similar to those secreted from the control group, but the amounts decreased during cultivation with A. culbertsoni lysate. These results suggest that pathogenic A. culbertsoni induces the cytopathic effects in primary-culture rat microglial cells, with the effects characterized by necrosis of microglial cells and changes in levels of secretion of TNF-α and IL-1β from microglial cells.
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