Gerlic Motti, Horowitz Jacob, Farkash Shai, Horowitz Shulamith
Department of Microbiology and Immunology, Faculty of Health Sciences, Soroka University Medical Center, Ben-Gurion University of the Negev, Beer-Sheva, Israel, 84105.
Cell Microbiol. 2007 Jan;9(1):142-53. doi: 10.1111/j.1462-5822.2006.00774.x. Epub 2006 Aug 2.
Mycoplasma have been shown to be involved in the alteration of several eukaryotic cell functions, such as cytokine production, gene expression and more. We have previously reported that infection of human myelomonocytic U937 cell line with live Mycoplasma fermentans (M. fermentans) inhibited tumour necrosis factor (TNF-alpha)-induced apoptosis. Mycoplasmal membrane lipoproteins are considered to be the most potent initiators of inflammatory reactions in mycoplasmal infections. The aim of this study was to clarify whether the inhibitory effect on TNFalpha-induced apoptosis is exerted by M. fermentans lipoproteins (LPMf). A significant reduction in TNFalpha-induced apoptosis was demonstrated by stimulation of U937 cells with M. fermentans total proteins, LPMf or MALP-2 (M. fermentans synthetic lipopeptide), but not with M. fermentans hydrophilic protein preparation (AqMf). To investigate the mechanism of M. fermentans antiapoptotic effect, the reduction of mitochondrial transmembrane potential (delta psi m) was measured. M. fermentans total proteins LPMf and MALP-2, but not AqMf, inhibited the reduction of delta psi m. In addition, M. fermentans total proteins LPMf and MALP-2, but not AqMf, downregulated the formation of active caspase-8. NF-kappaB was transactivated in cells treated with M. fermentans lipoproteins, and was essential for host cell survival, but not for the inhibition of TNFalpha-induced apoptosis by LPMf. Our results suggest that the inhibitory effect exerted by M. fermentans on TNFalpha-induced apoptosis in U937 cells is due to the membrane lipoproteins of these bacteria.
支原体已被证明与多种真核细胞功能的改变有关,如细胞因子产生、基因表达等。我们之前报道过,用活的发酵支原体(M. fermentans)感染人骨髓单核细胞U937细胞系可抑制肿瘤坏死因子(TNF-α)诱导的细胞凋亡。支原体膜脂蛋白被认为是支原体感染中炎症反应最有效的启动因子。本研究的目的是阐明发酵支原体脂蛋白(LPMf)是否对TNF-α诱导的细胞凋亡具有抑制作用。用发酵支原体总蛋白、LPMf或MALP-2(发酵支原体合成脂肽)刺激U937细胞,可显著降低TNF-α诱导的细胞凋亡,但用发酵支原体亲水性蛋白制剂(AqMf)刺激则无此效果。为了研究发酵支原体抗凋亡作用的机制,我们检测了线粒体跨膜电位(δψm)的降低情况。发酵支原体总蛋白、LPMf和MALP-2可抑制δψm的降低,而AqMf则无此作用。此外,发酵支原体总蛋白、LPMf和MALP-2可下调活性半胱天冬酶-8的形成,而AqMf则无此作用。在用发酵支原体脂蛋白处理的细胞中,NF-κB被激活,它对宿主细胞存活至关重要,但对LPMf抑制TNF-α诱导的细胞凋亡并非必需。我们的结果表明,发酵支原体对U937细胞中TNF-α诱导的细胞凋亡的抑制作用是由于这些细菌的膜脂蛋白所致。