Bermeo Sandra, Al-Saedi Ahmed, Kassem Moustapha, Vidal Christopher, Duque Gustavo
Sydney Medical School Nepean, The University of Sydney, Penrith, NSW, Australia.
Facultad de Ciencias Básicas y Biomédicas, Universidad Simón Bolívar, Barranquilla, Colombia.
J Cell Biochem. 2017 Dec;118(12):4425-4435. doi: 10.1002/jcb.26096. Epub 2017 Jul 31.
Mutations in MAN1, a protein of the nuclear envelope, cause bone phenotypes characterized by hyperostosis. The mechanism of this pro-osteogenic phenotype remains unknown. We increased and decreased MAN1 expression in mesenchymal stem cells (MSC) upon which standard osteogenic and adipogenic differentiation were performed. MAN1 knockdown increased osteogenesis and mineralization. In contrast, osteogenesis remained stable upon MAN1 overexpression. Regarding a mechanism, we found that low levels of MAN1 facilitated the nuclear accumulation of regulatory smads and smads-related complexes, with a concurrently high expression of nuclear β-Catenin. In addition, we found adipogenesis to be decreased in both conditions, although predominantly affected by MAN1 overexpression. Finally, lamin A, a protein of the nuclear envelope that regulates MSC differentiation, was unaffected by changes in MAN1. In conclusion, our studies demonstrated that lower levels of MAN1 in differentiating MSC are associated with higher osteogenesis and lower adipogenesis. High levels of MAN1 only affected adipogenesis. These effects could have an important role in the understanding of the role of the proteins of the nuclear envelope in bone formation. J. Cell. Biochem. 118: 4425-4435, 2017. © 2017 Wiley Periodicals, Inc.
核膜蛋白MAN1的突变会导致以骨质增生为特征的骨骼表型。这种促骨生成表型的机制尚不清楚。我们在间充质干细胞(MSC)中增加和降低MAN1的表达,并对其进行标准的成骨和成脂分化。MAN1基因敲低会增加成骨作用和矿化。相反,MAN1过表达时成骨作用保持稳定。关于其机制,我们发现低水平的MAN1促进了调节性smads和smads相关复合物的核内积累,同时核β-连环蛋白表达升高。此外,我们发现两种情况下脂肪生成均减少,不过主要受MAN1过表达的影响。最后,核膜蛋白lamin A可调节MSC分化,其不受MAN1变化的影响。总之,我们的研究表明,分化的MSC中较低水平的MAN1与较高的成骨作用和较低的脂肪生成有关。高水平的MAN1仅影响脂肪生成。这些效应对于理解核膜蛋白在骨形成中的作用可能具有重要意义。《细胞生物化学杂志》2017年第118卷:4425 - 4435页。© 2017威利期刊公司