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丙酮酸和尿苷对培养的U937-rho零细胞的分化作用。

Differentiation effect of pyruvate and uridine on cultured U937-rho degrees cells.

作者信息

Liu Yishan, Geng Li, Suo Zhenhe

机构信息

Department of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

出版信息

Ultrastruct Pathol. 2009 Jul-Aug;33(4):160-4. doi: 10.1080/01913120902889187.

Abstract

The human pro-monocytic leukemia U937 cell line was previously reported to become rho degrees cells after a long-term ethidium bromide exposure. In the authors' extensive PCR studies with different pairs of primers for the mtDNA molecule they showed that these U937-rho degrees cells, after being cultured in their laboratory for a time, did replete their mtDNA. That the cells grew well in the normal medium (RPMI 1640 plus 10% fetal calf serum and 2 mM l-glutamine) as the parental cells also suggests that these cells contain functional mitochondria and mtDNA molecules. Further experiments showed that the cells cultured in the medium with pyruvate and uridine rather rapidly and strongly adhered on the culture flask walls while the cells cultured in the medium without pyruvate and uridine either floated or only very loosely covered the culture flask walls. Ultrastructural examination showed that the floating cells, which were often found in the culture without pyruvate and uridine, were rather similar to monocytes in nature, like the original U937 cells, while the attached larger cells appearing earlier in the culture with pyruvate and uridine demonstrated macrophage differentiation, indicating a differentiation effect of pyruvate and uridine on the cells.

摘要

据先前报道,人原单核细胞白血病U937细胞系在长期暴露于溴化乙锭后会变成ρ⁰细胞。在作者使用针对线粒体DNA(mtDNA)分子的不同引物对进行的广泛聚合酶链反应(PCR)研究中,他们发现这些U937 - ρ⁰细胞在实验室培养一段时间后确实补充了它们的mtDNA。这些细胞在正常培养基(RPMI 1640加10%胎牛血清和2 mM L - 谷氨酰胺)中生长良好,这与亲代细胞一样,表明这些细胞含有功能性线粒体和mtDNA分子。进一步的实验表明,在含有丙酮酸和尿苷的培养基中培养的细胞相当迅速且强烈地附着在培养瓶壁上,而在不含丙酮酸和尿苷的培养基中培养的细胞要么漂浮着,要么只是非常松散地覆盖在培养瓶壁上。超微结构检查显示,在不含丙酮酸和尿苷的培养物中经常发现的漂浮细胞,在本质上与单核细胞相当相似,就像原始的U937细胞一样,而在含有丙酮酸和尿苷的培养物中较早出现的附着的较大细胞表现出巨噬细胞分化,表明丙酮酸和尿苷对细胞有分化作用。

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