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首页> 外文期刊>Journal of cellular biochemistry. >Transport of inorganic phosphate in primary cultures of chondrocytes isolated from the tibial growth plate of normal adolescent chickens.
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Transport of inorganic phosphate in primary cultures of chondrocytes isolated from the tibial growth plate of normal adolescent chickens.

机译:从正常青春期鸡胫骨生长板分离的软骨细胞原代培养物中无机磷酸盐的运输。

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This report describes Pi transport activity in chondrocytes isolated from the growth plate (GP) of normal adolescent chickens grown in primary cell culture. Our recent work showed that Pi transport in matrix vesicles (MV) isolated from normal GP cartilage was not strictly Na(+)-dependent, whereas previously characterized Pi transport from rachitic GP cartilage MV was. This Na(+)-dependent Pi transporter (NaPiT), a member of the Type III Glvr-1 gene family, is expressed only transiently during early differentiation of GP cartilage, is enhanced by Pi-deficiency, and is most active at pH 6.8. Since GP mineralization requires abundant Pi and occurs under slightly alkaline conditions, it seemed unlikely that this type of Pi transporter was solely responsible for Pi uptake during normal GP development. Therefore we asked whether the lack of strict Na(+)-dependency in Pi transport seen in normal MV was also evident in normal GP chondrocytes. In fact, cellular Pi transport was found not to be strictly Na(+)-dependent, except for a brief period early in the culture. Choline could equally serve as a Na(+) substitute. Activity of choline-supported Pi transport was optimum at pH 7.6-8.0. In addition, prior exposure of the cells to elevated extracellular Pi (2-3 mM) strongly enhanced subsequent Pi uptake, which appeared to depend on prior loading of the cells with mineral ions. Prevention of Pi loading by pretreatment with Pi transport inhibitors not only inhibited subsequent cellular Pi uptake, it also blocked mineral formation. Treatment with elevated extracellular Pi did not induce apoptosis in these GP chondrocytes. J. Cell. Biochem. 86: 475-489, 2002.
机译:该报告描述了从原代细胞培养中生长的正常青春期鸡的生长板(GP)分离的软骨细胞中的Pi转运活性。我们最近的工作表明,从正常GP软骨分离的基质囊泡(MV)中的Pi转运并非严格依赖Na(+)依赖性,而以前从轮状GP软骨MV表征的Pi转运是Na依赖性的。这种Na(+)依赖的Pi转运蛋白(NaPiT),是III型Glvr-1基因家族的成员,仅在GP软骨的早期分化过程中瞬时表达,通过Pi缺乏增强,并且在pH 6.8时最活跃。由于GP的矿化作用需要大量的Pi并在弱碱性条件下发生,因此在正常GP发育过程中,这种类型的Pi转运体似乎不可能完全负责Pi的吸收。因此,我们问正常的MV中是否也缺乏在正常MV中看到的Pi转运中缺乏严格的Na(+)依赖性。实际上,发现细胞Pi的转运不是严格的Na(+)依赖性,只是在培养初期有短暂的时间。胆碱同样可以用作Na(+)的替代物。胆碱支持的Pi转运的活性在pH 7.6-8.0时最佳。此外,先前将细胞暴露于升高的细胞外Pi(2-3 mM)会大大增强随后的Pi吸收,这似乎取决于先前向细胞中加载的无机离子。通过用Pi转运抑制剂进行预处理来预防Pi的装载不仅抑制了随后的细胞对Pi的吸收,而且还阻止了矿物质的形成。用升高的细胞外Pi进行治疗不会诱导这些GP软骨细胞凋亡。 J.细胞。生化。 86:475-489,2002。

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