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

  • Tuan Anh Vuong
  • , Yan Zhang
  • , June Kim
  • , Young Eun Leem
  • , Jong Sun Kang

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)330-335
Number of pages6
JournalBMB Reports
Volume57
Issue number7
DOIs
StatePublished - 2024

Keywords

  • Arginine methylation
  • BMP signaling pathway
  • Mesenchymal stem cells
  • Osteogenesis
  • Prmt7

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