Prmt7 is required for the osteogenic differentiation of mesenchymal stem cells via modulation of BMP signaling

被引:3
作者
Vuong, Tuan Anh [1 ]
Zhang, Yan [1 ]
Kim, June [1 ]
Leem, Young-Eun [1 ]
Kang, Jong-Sun [1 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Dept Mol Cell Biol, Suwon 16419, South Korea
基金
新加坡国家研究基金会;
关键词
Arginine methylation; BMP signaling pathway; Mesen- chymal stem cells; Osteogenesis; Prmt7; METHYLATION;
D O I
10.5483/BMBRep.2023-0203
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Arginine methylation, which is catalyzed by protein arginine methyltransferases (Prmts), is known to play a key role in various biological processes. However, the function of Prmts in osteogenic differentiation of mesenchymal stem cells (MSCs) has not been clearly understood. In the current study, we attempted to elucidate a positive role of Prmt7 in osteogenic differentiation. Prmt7-depleted C3H/10T1/2 cells or bone marrow mesenchymal stem cells (BMSCs) showed the attenuated expression of osteogenic specific genes and Alizarin red staining compared to the wild-type cells. Furthermore, we found that Prmt7 deficiency reduced the activation of bone morphogenetic protein (BMP) signaling cascade, which is essential for the regulation of cell fate commitment and osteogenesis. Taken together, our data indicate that Prmt7 plays important regulatory roles in osteogenic differentiation. [BMB Reports 2024; 57(7): 330-335]
引用
收藏
页码:330 / 335
页数:6
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