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  3. Endothelin-1/endothelin B receptor signalling mediates Prx1+ skeletal stem cells senescence: A driver of osteoporotic bone loss

Endothelin-1/endothelin B receptor signalling mediates Prx1+ skeletal stem cells senescence: A driver of osteoporotic bone loss

  • J Orthop Translat. 2026 Feb 18:57:101048. doi: 10.1016/j.jot.2026.101048.
Zhou Zou 1 2,  Weiyuan Gong 2 3,  Xuan Lu 2,  Yuqi Zhang 2 4,  Manting Au 2,  Junxin Lin 5,  Hongwei Ouyang 6,  Guozhi Xiao 3,  Bin Tang 1,  Chunyi Wen 2 7
Affiliations

Affiliations

  • 1 Department of Biomedical Engineering, Southern University of Science and Technology, Shenzhen, Guangdong, China.
  • 2 Department of Biomedical Engineering, The Hong Kong Polytechnic University, Hong Kong, China.
  • 3 Department of Biochemistry, School of Medicine, Southern University of Science and Technology, Guangdong Provincial Key Laboratory of Cell Microenvironment and Disease Research, Shenzhen Key Laboratory of Cell Microenvironment, Shenzhen, Guangdong, China.
  • 4 National Center for Applied Mathematics Shenzhen, Southern University of Science and Technology, Shenzhen, Guangdong, China.
  • 5 School of Medicine, Taizhou University, Taizhou, Zhejiang, China.
  • 6 Zhejiang University-University of Edinburgh Institute, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
  • 7 Research Institute of Smart Ageing, The Hong Kong Polytechnic University, Hong Kong, China.
PMID: 41757294 DOI: 10.1016/j.jot.2026.101048
Abstract

Background: Stem cells residing in the perivascular niche are critical for skeletal homeostasis. Vascular endothelin-1 (ET-1) controls stem cell fate in development, but its role in the exhaustion of skeletal stem cells (SSCs) and subsequent bone degeneration in osteoporosis remains poorly understood. This study aimed to determine whether ET-1 signalling drives SSCs senescence and to elucidate the underlying mechanisms.

Methods: We utilised a combination of human single-cell RNA Sequencing datasets, murine models of ageing and ovariectomy (OVX), and an endothelial-specific ET-1 overexpression transgenic (TET-1) mouse model. In vitro studies on mesenchymal stem cells (MSCs) employed ET-1 challenge with and without receptor-specific antagonists (BQ123 for ETAR, BQ788 for ETBR). The mechanism was further probed using transcriptomic profiling and validated in vivo through Prx1+ SSCs-specific ETBR knockout (Prx1-Cre;ETBR fl/fl ) and pharmacological inhibition with the ETBR antagonist BQ788.

Results: In aged and OVX mice, ETBR expression was significantly upregulated in SSCs concurrent with bone loss. Transgenic ET-1 overexpression recapitulated an aged bone phenotype, inducing SSCs senescence and accelerating bone loss. In vitro, ET-1 triggered MSCs senescence and Reactive Oxygen Species (ROS) accumulation. Such effects were specifically abrogated by ETBR, but not ETAR. Transcriptomic analysis revealed that ET-1/ETBR signalling synergistically dysregulates the PI3K-AKT and p53 pathways to orchestrate senescence. Critically, both genetic knockout of ETBR in Prx1+ SSCs and pharmacological inhibition with BQ788 mitigated oxidative stress, reduced cellular senescence, and preserved bone mass in OVX and aged mice.

Conclusion: This study identified the ET-1/ETBR signalling axis as a critical driver of osteoporosis by promoting ROS-mediated SSCs senescence. We established a link between vascular ageing and skeletal decline.

The translational potential of this article: This study positioned ETBR blockade as a promising novel therapeutic strategy for osteoporosis. By targeting the upstream driver of SSCs exhaustion, ETBR inhibition offers a potential paradigm shift from palliative care to proactive rejuvenation of the osteogenic niche. This approach could counteract both postmenopausal and age-related bone loss by restoring the bone-forming potential of the skeleton, addressing a significant unmet clinical need.

Keywords

Ageing; Cellular senescence; Endothelin type B receptor; Endothelin-1; Osteoporosis; Skeletal stem cells.

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