Dipartimento di Scienze Biomediche e Cliniche L. Sacco, Università di Milano, Milano, I-20157, Italy.
Dipartimento di Scienze Biomediche e Cliniche L. Sacco, Università di Milano, Milano, I-20157, Italy.
Biochem Biophys Res Commun. 2019 May 21;513(1):159-165. doi: 10.1016/j.bbrc.2019.03.178. Epub 2019 Apr 2.
The magnesium transporters TRPM7 and MagT1 are overexpressed in osteoblastogenesis. We have shown that silencing either TRPM7 or MagT1 accelerates the osteogenic differentiation of human bone mesenchymal stem cells. Here we demonstrate that the simultaneous downregulation of TRPM7 and MagT1 inhibits cell growth and activates autophagy, which is required in the early phases of osteoblastogenesis. In TRPM7/MagT1 downregulating cells the expression of two transcription factors required for activating osteogenesis, i.e. RUNX2 and OSTERIX, is induced more than in the controls both in the presence and in the absence of osteogenic stimuli, while COL1A1 is upregulated in co-silencing cells as much as in the controls. This explains why we found no differences in calcium deposition. We conclude that one of the two transporters should be expressed to accelerate osteogenic differentiation.
镁转运蛋白 TRPM7 和 MagT1 在成骨细胞分化中过表达。我们已经表明,沉默 TRPM7 或 MagT1 中的任一个都会加速人骨髓间充质干细胞的成骨分化。在这里,我们证明同时下调 TRPM7 和 MagT1 会抑制细胞生长并激活自噬,这在成骨细胞发生的早期阶段是必需的。在下调 TRPM7 和 MagT1 的细胞中,两种转录因子的表达被诱导,这两种转录因子对于激活成骨作用是必需的,即 RUNX2 和 OSTERIX,在有和没有成骨刺激的情况下都比对照组诱导得更多,而 COL1A1 在共沉默细胞中的上调与对照组一样多。这解释了为什么我们在钙沉积方面没有发现差异。我们得出结论,为了加速成骨分化,两种转运蛋白之一应该表达。