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Regulation of cell proliferation and cell density by the inorganic phosphate transporter PiT1

机译:无机磷酸盐转运蛋白PiT1对细胞增殖和细胞密度的调节

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摘要

AbstactBackgroundThe inorganic phosphate (Pi) transporter, PiT1 (SLC20A1), is ubiquitously expressed in mammalian cells. It has previously been shown that down-regulation of PiT1 severely impaired the proliferation of two transformed human cells lines, HepG2 and HeLa, and the tumorigenicity of HeLa cells in nude mice. Moreover, PiT1 knock-out mice do not survive past E12.5 and from E10.5, the embryos were found to be growth-retarded and showed reduced proliferation of liver cells. Isolated mouse embryonic fibroblasts with knocked out as well as reduced PiT1 expression levels also exhibited impaired proliferation. Together these results suggest that a certain level of PiT1 is important for proliferation. We have here investigated the role of PiT1 in regulation of cell proliferation using two strictly density-inhibited cells lines, the murine MC3T3-E1 and NIH3T3 cells.
机译:摘要无机磷酸盐(Pi)转运蛋白PiT1(SLC20A1)在哺乳动物细胞中普遍表达。先前已经显示,PiT1的下调严重损害了两种转化的人类细胞系HepG2和HeLa的增殖以及HeLa细胞在裸鼠中的致瘤性。此外,剔除PiT1的小鼠不能存活到E12.5以后,从E10.5起,发现胚胎发育迟缓,并且肝细胞增殖减少。具有敲除以及降低的PiT1表达水平的分离的小鼠胚胎成纤维细胞也显示出受损的增殖。这些结果共同表明,一定水平的PiT1对增殖很重要。我们在这里使用两种严格抑制密度的细胞系鼠MC3T3-E1和NIH3T3细胞研究了PiT1在调控细胞增殖中的作用。

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