首页> 美国卫生研究院文献>International Journal of Biomedical Science : IJBS >Induction of Constitutive High-Level Expression of c-Myc in 32D Cells by Mycoplasmas is Associated with their Ability to Prevent Apoptosis and Induce Malignant Transformation
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Induction of Constitutive High-Level Expression of c-Myc in 32D Cells by Mycoplasmas is Associated with their Ability to Prevent Apoptosis and Induce Malignant Transformation

机译:支原体诱导c-Myc在32D细胞中的组成型高水平表达与其预防凋亡和诱导恶性转化的能力有关。

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摘要

Our previous studies showed that mycoplasmas prevented apoptosis and induced the malignant transformation of mammalian cells. Other studies indicate that c-Myc plays an important role in promoting apoptosis and malignant transformation of cells. To understand the role of c-Myc in the mycoplasma induced apoptosis prevention and malignant cell transformation, 32D cells, an IL-3 dependent cell line, were infected and transformed by different species of mycoplasmas. The expression of Myc and ras gene families, apoptosis and the cell cycle during the infection and transformation were examined. Results showed that c-Myc expression was significantly increased in mycoplasma transformed 32D cells. Withdrawal of IL-3 substantially decreased c-Myc expression and led to cell cycle arrest at the G1 phase followed by rapid apoptosis. Infection by M. fermentans or M. penetrans not only alleviated the sharp decrease of c-Myc expression, rescued 32D cells from cell-cycle arrest and prevented apoptosis in IL-3-free culture, but also induced autonomous growth of 32D cells. Although M. hominis and M. salivarium had the ability neither to prevent apoptosis nor to induce malignant transformation, they were still able to rescue the cells from cell cycle arrest. The expression of ras family did not change significantly during the infection and transformation. These results suggest that constitutive expression of c-Myc appears to be associated with the continuous growth and malignant transformation of 32D cells induced by M. fermentans and M. penetrans, but not with rescuing the cell cycle arrest by the mycoplasmas.
机译:我们以前的研究表明,支原体阻止了细胞凋亡并诱导了哺乳动物细胞的恶性转化。其他研究表明,c-Myc在促进细胞凋亡和恶性转化中起重要作用。为了理解c-Myc在支原体诱导的凋亡预防和恶性细胞转化中的作用,感染了32D细胞,一种IL-3依赖性细胞系,并被不同种类的支原体感染和转化。检测了Myc和ras基因家族的表达,细胞凋亡以及感染和转化过程中的细胞周期。结果显示,在支原体转化的32D细胞中c-Myc表达显着增加。 IL-3的撤离大大降低了c-Myc表达,并导致细胞周期停滞在G1期,随后迅速凋亡。发酵曲霉菌或佩恩特霉菌的感染不仅减轻了c-Myc表达的急剧下降,从细胞周期停滞中拯救了32D细胞,并防止了无IL-3培养物中的细胞凋亡,而且还诱导了32D细胞的自主生长。尽管人型支原体和唾液支原体既没有防止细胞凋亡也没有诱导恶性转化的能力,但它们仍然能够从细胞周期停滞中拯救细胞。 ras家族的表达在感染和转化过程中没有显着改变。这些结果表明,c-Myc的组成型表达似乎与发酵支原体和penetrans支原体诱导的32D细胞的持续生长和恶性转化有关,但与拯救支原体的细胞周期停滞无关。

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