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1α,25 - 二羟维生素D3处理的大鼠成骨细胞样细胞的mRNA诱导非洲爪蟾卵母细胞中钠依赖性磷酸盐(NadPi)转运的表达。

Expression of sodium-dependent phosphate (NadPi) transport in Xenopus laevis oocytes induced by mRNA from 1 alpha, 25-dihydroxyvitamin D3-treated rat osteoblast-like cells.

作者信息

Veldman C M, Markovich D, Schmid C, Murer H

机构信息

Department of Internal Medicine, University Hospital, Zürich, Switzerland.

出版信息

Pflugers Arch. 1995 May;430(1):64-7. doi: 10.1007/BF00373840.

Abstract

Injection of messenger ribonucleic acid (mRNA) isolated from 1 alpha, 25-dihydroxyvitamin D3-treated osteoblast-like (PyMS) cells leads to an enhanced sodium-dependent phosphate (NadPi) transport in Xenopus laevis oocytes, when compared to untreated cells. After mRNA size fractionation, mRNA with an average size of 2.2-3.8 kilobases showed up to a 1.8-fold stimulation of NadPi transport encoding either directly a NadPi transporter(s) or proteins controlling their activity. No hybridization was observed in Northern blots with RNA from rat bone or PyMS cells with the recently cloned rat renal brush border NadPi transporter NaPi-2; hybrid depletion with a NaPi-2 antisense oligonucleotide did not abolish the PyMS mRNA-induced NadPi transport in oocytes. We present the first evidence for functional expression in Xenopus laevis oocytes of a new type of NadPi transport system in bone cells, which is different from the renal type.

摘要

与未处理的细胞相比,将从1α,25 - 二羟基维生素D3处理的成骨细胞样(PyMS)细胞中分离出的信使核糖核酸(mRNA)注入非洲爪蟾卵母细胞后,会导致钠依赖性磷酸盐(NadPi)转运增强。对mRNA进行大小分级分离后,平均大小为2.2 - 3.8千碱基的mRNA对NadPi转运的刺激作用高达1.8倍,这些mRNA要么直接编码NadPi转运蛋白,要么编码控制其活性的蛋白质。用来自大鼠骨骼或PyMS细胞的RNA与最近克隆的大鼠肾刷状缘NadPi转运蛋白NaPi - 2进行Northern印迹杂交时未观察到杂交信号;用NaPi - 2反义寡核苷酸进行杂交缺失实验并没有消除PyMS mRNA诱导的卵母细胞中NadPi转运。我们首次证明了骨细胞中一种新型NadPi转运系统在非洲爪蟾卵母细胞中的功能性表达,该系统与肾型不同。

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