Journal of Bone and Mineral ResearchBioengineeringPeer-reviewed journal article
Ablation of Proliferating Osteoblast Lineage Cells After Fracture Leads to Atrophic Nonunion in a Mouse Model
K. R. Hixon, J. A. McKenzie, D. A. Sykes, S. Yoneda, A. Hensley, E. G. Buettmann, H. Zheng, D. Skouteris, A. McAlinden, A. N. Miller, M. J. Silva
Abstract
Nonunion is defined as the permanent failure of a fractured bone to heal, often necessitating surgical intervention. Atrophic nonunions are a subtype that are particularly difficult to treat. Animal models of atrophic nonunion are available; however, these require surgical or radiation-induced trauma to disrupt periosteal healing. These methods are invasive and not representative of many clinical nonunions where osseous regeneration has been arrested by a "failure of biology". We hypothesized that arresting osteoblast cell proliferation after fracture would lead to atrophic nonunion in mice. Using mice that express a thymidine kinase (tk) "suicide gene" driven by the 3.6Col1a1 promoter (Col1-tk), proliferating osteoblast lineage cells can be ablated upon exposure to the nucleoside analog ganciclovir (GCV). Wild-type (WT; control) and Col1-tk littermates were subjected to a full femur fracture and intramedullary fixation at 12 weeks age. We confirmed abundant tk+ cells in fracture callus of Col-tk mice dosed with water or GCV, specifically many osteoblasts, osteocytes, and chondrocytes at the cartilage-bone interface. Histologically, we observed altered callus composition in Col1-tk mice at 2 and 3 weeks post fracture, with significantly less bone and more fibrous tissue. Col1-tk mice, monitored for 12 weeks with in vivo radiographs and microCT scans, had delayed bone bridging and reduced callus size. Following sacrifice, ex vivo microCT and histology demonstrated failed union with residual bone fragments and fibrous tissue in Col1-tk mice. Biomechanical testing demonstrated a failure to recover torsional strength in Col1-tk mice, in contrast to WT. Our data indicates that suppression of proliferating osteoblast-lineage cells for at least 2 weeks after fracture blunts the formation and remodeling of a mineralized callus leading to a functional nonunion. We propose this as a new murine model of atrophic nonunion.
- organism: mouse
- assay: imaging
- research focus: development & morphogenesis
- approach: experimental assay
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Proliferation of Early and Mature Osteoblasts Is Required for Bone Fracture Healing in Mice
Nicole R. Gould, Andre F. Coello, … Matthew J. Silva·bioRxiv·May 27, 2025
- Maladaptive immune-fibrotic axis drives impaired long bone regeneration under mechanical instability
M. Patrick, J. Ahn, … R. T. Annamalai·bioRxiv·Oct 26, 2023
- Murine Progeria Model Exhibits Delayed Fracture Healing with Dysregulated Local Immune Response
Victoria R. Duke, Marc J. Philippon, … Chelsea S. Bahney·bioRxiv·May 29, 2024
- Improved Methodology for Studying Postnatal Osteogenesis via Intramembranous Ossification in a Murine Bone Marrow Injury Model
Marta Stetsiv, Matthew Wan, … Archana Sanjay·Journal of Visualized ExperimentsPeer-reviewed·Feb 7, 2025
- CD47 is Required for Mesenchymal Progenitor Proliferation and Fracture Repair
Robert L. Zondervan, Christina A. Capobianco, … Kurt David Hankenson·Bone ResearchPeer-reviewed·Mar 2, 2025
- Osteocyte death and bone overgrowth in mice lacking Fibroblast Growth Factor Receptors 1 and 2 in mature osteoblasts and osteocytes
Jennifer A. McKenzie, Craig R. Smith, … David M. Ornitz·Journal of Bone and Mineral ResearchPeer-reviewed·Jun 17, 2019