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Potential malignant transformation in the gastric mucosa of immunodeficient mice with persistent Mycoplasma penetrans infection

机译:持续性支原体感染的免疫缺陷小鼠胃黏膜中潜在的恶性转化

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摘要

Mycoplasma infection has been reported in immunocompromised cancer patients; nevertheless, it is not clear if persistent Mycoplasma infection could facilitate the proliferation of cancer cells in immunocompromised organisms. The aim of this study was to examine the relationship between persistent Mycoplasma infection and malignant transformation in an immunodeficient host model. Immunodeficient mouse model was established using cyclophosphamide and mice gastric mucosal cells were infected with Mycoplasma penetrans (Mpe). After 18 weeks, mice were sacrificed and gastric mucosal Mpe infected cells were identified by fluorescence in situ hybridization (FISH). Moreover, pathological and ultrastructural changes in mice gastric mucosa were evaluated and the expression of multiple proto-oncogenes was examined by Western blot. Our data show that Mpe infection was detected in the blood of immunodeficient mice and Mpe persistent infection in mice gastric mucosa was confirmed by FISH. There were pathological and ultrastructural malignant transformation occurred in the gastric mucosa of infected mice compared to control mice. Mpe infected mice showed lower expression of p53 and p21 and higher H-ras expression compared to the control group. Moreover, expression of NF-κB p65 subunit increased in Mpe infected mice, similar to the TNF-α expression. Bax expression in gastric mucosa of Mpe infected mice was lower while Bcl-2 expression was higher than in the uninfected control group. Collectively these data demonstrate that persistent Mpe infection is associated with aberrant expression of multiple proto-oncogenes in gastric mucosa of immunodeficient mice which potentially facilitate the malignant transformation.
机译:在免疫功能低下的癌症患者中已报道支原体感染。然而,尚不清楚持续性支原体感染是否能促进免疫受损生物体内癌细胞的增殖。这项研究的目的是在免疫缺陷宿主模型中检查持续性支原体感染与恶性转化之间的关系。使用环磷酰胺建立免疫缺陷的小鼠模型,并将小鼠胃粘膜细胞感染支原体支原体(Mpe)。 18周后,处死小鼠,并通过荧光原位杂交(FISH)鉴定胃粘膜Mpe感染的细胞。此外,评估了小鼠胃粘膜的病理学和超微结构变化,并通过蛋白质印迹法检测了多种原癌基因的表达。我们的数据表明,在免疫缺陷小鼠的血液中检测到了Mpe感染,而FISH证实了小鼠胃粘膜中的Mpe持续感染。与对照组相比,感染小鼠的胃黏膜发生了病理学和超微结构的恶性转化。与对照组相比,受Mpe感染的小鼠的p53和p21表达较低,而H-ras表达较高。此外,在Mpe感染的小鼠中NF-κBp65亚基的表达增加,类似于TNF-α的表达。与未感染的对照组相比,Mpe感染小鼠的胃黏膜中Bax表达较低,而Bcl-2表达较高。这些数据共同表明,持续的Mpe感染与免疫缺陷小鼠胃粘膜中多种原癌基因的异常表达有关,这可能促进恶性转化。

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