中国神经再生研究(英文版) ›› 2026, Vol. 21 ›› Issue (7): 2830-2831.doi: 10.4103/NRR.NRR-D-25-00290

• 观点:退行性病与再生 • 上一篇    

转录因子NR2F1参与帕金森病

  

  • 出版日期:2026-07-15 发布日期:2025-10-20

Transcription factor NR2F1 is involved in Parkinson’s disease

Annemarie de Vries, Silvia Bolognin*   

  1. MERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, the Netherlands
  • Online:2026-07-15 Published:2025-10-20
  • Contact: Silvia Bolognin, PhD, silvia.bolognin@maastrichtuniversity.nl.

摘要: https://orcid.org/0000-0002-1399-2999 (Silvia Bolognin) 

Abstract: Nuclear receptor subfamily 2 group F member 1 (NR2F1, also called COUP-TF1) is a transcription factor and part of the steroid/thyroid hormone receptor superfamily (Gay et al., 2002). NR2F1 is an orphan receptor that dimerizes to bind DNA and acts as a repressor as well as an activator of the target genes (Gay et al., 2002; Bertacchi et al., 2019; Bonzano et al., 2023). It was found recently to regulate the transcription of mitochondrial genes and to affect the morphology and mass of mitochondria (Bonzano et al., 2023). NR2F1 is mainly known for its pleiotropic role in neurodevelopment, but it has recently been connected to neurodegeneration in the context of Parkinson’s disease (PD) (Walter et al., 2021). This perspective summarizes the known functions of NR2F1 and offers a new perspective on its potential role in neurodegeneration.