Ferroptosis in Osteocytes as a Target for Protection Against Postmenopausal Osteoporosis

Abstract: Ferroptosis is a necrotic form of iron‐dependent regulatory cell death. Estrogen withdrawal can interfere with iron metabolism, which is responsible for the pathogenesis of postmenopausal osteoporosis (PMOP). Here, it is demonstrated that estrogen withdrawal induces iron accumulation in the skeleton and the ferroptosis of osteocytes, leading to reduced bone mineral density. Furthermore, the facilitatory effect of ferroptosis of osteocytes is verified in the occurrence and development of postmenopausal osteoporosis is associated with over activated osteoclastogenesis using a direct osteocyte/osteoclast coculture system and glutathione peroxidase 4 (GPX4) knockout ovariectomized mice. In addition, the nuclear factor erythroid derived 2‐related factor‐2 (Nrf2) signaling pathway is confirmed to be a crucial factor in the ferroptosis of osteocytic cells. Nrf2 regulates the expression of nuclear factor kappa‐B ligand (RANKL) by regulating the DNA methylation level of the RANKL promoter mediated by DNA methyltransferase 3a (Dnmt3a), which is as an important mechanism in osteocytic ferroptosis‐mediated osteoclastogenesis. Taken together, this data suggests that osteocytic ferroptosis is involved in PMOP and can be targeted to tune bone homeostasis.

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
Ferroptosis in Osteocytes as a Target for Protection Against Postmenopausal Osteoporosis ; day:17 ; month:01 ; year:2024 ; extent:20
Advanced science ; (17.01.2024) (gesamt 20)

Creator
Jiang, Zengxin
Qi, Guobin
He, Xuecheng
Yu, Yifan
Cao, Yuting
Zhang, Changqing
Zou, Weiguo
Yuan, Hengfeng

DOI
10.1002/advs.202307388
URN
urn:nbn:de:101:1-2024011814034958735322
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
15.08.2025, 7:24 AM CEST

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Associated

  • Jiang, Zengxin
  • Qi, Guobin
  • He, Xuecheng
  • Yu, Yifan
  • Cao, Yuting
  • Zhang, Changqing
  • Zou, Weiguo
  • Yuan, Hengfeng

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