Zhang Shimin, Lo Shyh-Ching
Division of Molecular Pathobiology, Department of Infectious and Parasitic Diseases Pathology, American Registry of Pathology, Armed Forces Institute of Pathology, 14th Street and Alaska Avenue NW, Washington, DC 20306-6000, USA.
Curr Microbiol. 2007 May;54(5):388-95. doi: 10.1007/s00284-006-0491-x. Epub 2007 May 5.
We previously showed that mycoplasmal infection effectively prevented apoptosis of infected cells, whereas other researchers have indicated that mycoplasmal infection promoted apoptosis. To understand the mechanism underlying this discrepancy, five different species of mycoplasmas were investigated for their effects on apoptosis of interleukin (IL)-3-dependent 32D cells. Results revealed that Mycoplasma fermentans and M. penetrans effectively supported continuous growth of 32D cells after IL-3 withdrawal. M. fermentans was more potent than M. penetrans. This effect was achieved by way of preventing apoptosis and stimulating cell proliferation. On the contrary, M. hominis and M. salivarium accelerated apoptosis of 32D cells. M. genitalium had no significant effect on apoptosis. The RNase protection assay indicated that the proapoptotic and antiapoptotic mycoplasmas altered the expression of major apoptosis regulatory genes differently. The difference in apoptosis regulatory gene expression induced by different species of mycoplasmas might be accountable for their effects on host cell apoptosis.
我们之前表明,支原体感染可有效防止受感染细胞凋亡,而其他研究人员则指出支原体感染会促进细胞凋亡。为了解这种差异背后的机制,我们研究了五种不同的支原体对白细胞介素(IL)-3依赖的32D细胞凋亡的影响。结果显示,发酵支原体和穿透支原体在IL-3撤除后能有效支持32D细胞的持续生长。发酵支原体比穿透支原体的作用更强。这种作用是通过防止细胞凋亡和刺激细胞增殖实现的。相反,人型支原体和唾液支原体加速了32D细胞的凋亡。生殖支原体对细胞凋亡没有显著影响。核糖核酸酶保护试验表明,促凋亡和抗凋亡支原体对主要凋亡调节基因的表达改变不同。不同种类支原体诱导的凋亡调节基因表达差异可能是它们对宿主细胞凋亡产生影响的原因。