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NXNL1 negatively regulates osteoblast differentiation via GDF15-induced PP2A Cα dependent manner in MC3T3-E1 cells.

Abstract
Controlling the level of intracellular reactive oxygen species (ROS) is important for the survival and differentiation of osteoblasts. Intracellular ROS levels are controlled by antioxidant enzymes that modulate the redox state of the cell. Nucleoredoxin-like 1 (NXNL1) is an antioxidant enzyme that increases the viability of rod and cone cells by protecting them from oxidative stress, and is a potential pharmacological target for the treatment of retinitis pigmentosa. The present study investigated the role of NXNL on osteoblast differentiation of MC3T3-E1 preosteoblast cells. Results from qPCR experiments demonstrated that growth differentiation factor 15 (GDF15) increased NXNL1 expression, and that GDF15-induced NXNL1 decreased the expression of osteogenic genes such as distal-less homeobox 5 (Dlx5) and Runt-related transcription factor 2. Furthermore, NXNL1 also inhibits bone morphogenetic protein 2-induced phosphorylation of Smad1/5/9 and alkaline phosphatase activity. The inhibitory effects of NXNL1 on osteoblast differentiation were mediated by protein phosphatase 2A Cα (PP2A Cα). The expression of PP2A Cα was regulated by GDF15, and overexpression of PP2A Cα increased the expression of NXNL1. Taken together, our results demonstrate that NXNL1 inhibits osteoblast differentiation of MC3T3-E1 due to GDF15-induced expression of PP2A Cα.
AuthorsKyeong-Min Kim, Won-Gu Jang
JournalBioFactors (Oxford, England) (Biofactors) Vol. 48 Issue 1 Pg. 239-248 (Jan 2022) ISSN: 1872-8081 [Electronic] Netherlands
PMID34932831 (Publication Type: Journal Article)
Copyright© 2021 International Union of Biochemistry and Molecular Biology.
Chemical References
  • Gdf15 protein, mouse
  • Growth Differentiation Factor 15
  • Thioredoxins
  • PPP2CA protein, mouse
  • Protein Phosphatase 2
Topics
  • Animals
  • Cell Differentiation
  • Cell Line
  • Growth Differentiation Factor 15 (genetics)
  • Mice
  • Osteoblasts (cytology)
  • Osteogenesis
  • Protein Phosphatase 2 (genetics)
  • Thioredoxins (genetics)

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