4.6 Article

Molecular Identification of Spatially Distinct Anabolic Responses to Mechanical Loading in Murine Cortical Bone

期刊

JOURNAL OF BONE AND MINERAL RESEARCH
卷 37, 期 11, 页码 2277-2287

出版社

WILEY
DOI: 10.1002/jbmr.4686

关键词

BIOMECHANICS; MOLECULAR PATHWAYS-REMODELING; CELL; TISSUE SIGNALING-TRANSCRIPTION FACTORS; OSTEOPOROSIS; PRECLINICAL STUDIES

资金

  1. NSF [1636012]
  2. NSF GRFP [DGE-1650441]
  3. GAANN [P200A150273 J]
  4. Directorate For Engineering
  5. Div Of Civil, Mechanical, & Manufact Inn [1636012] Funding Source: National Science Foundation

向作者/读者索取更多资源

Osteoporosis affects over 200 million women worldwide, with one-third of them predicted to experience osteoporotic fractures in their lifetime. A study using a mouse model found that mechanical loading can stimulate bone formation, potentially identifying new pathways for oral treatment.
Osteoporosis affects over 200 million women worldwide, one-third of whom are predicted to suffer from an osteoporotic fracture in their lifetime. The most promising anabolic drugs involve administration of expensive antibodies. Because mechanical loading stimulates bone formation, our current data, using a mouse model, replicates the anabolic effects of loading in humans and may identify novel pathways amenable to oral treatment. Murine tibial compression produces axially varying deformations along the cortical bone, inducing highest strains at the mid-diaphysis and lowest at the metaphyseal shell. To test the hypothesis that load-induced transcriptomic responses at different axial locations of cortical bone would vary as a function of strain magnitude, we loaded the left tibias of 10-week-old female C57Bl/6 mice in vivo in compression, with contralateral limbs as controls. Animals were euthanized at 1, 3, or 24 hours post-loading or loaded for 1 week (n = 4-5/group). Bone marrow and cancellous bone were removed, cortical bone was segmented into the metaphyseal shell, proximal diaphysis, and mid-diaphysis, and load-induced differential gene expression and enriched biological processes were examined for the three segments. At each time point, the mid-diaphysis (highest strain) had the greatest transcriptomic response. Similarly, biological processes regulating bone formation and turnover increased earlier and to the greatest extent at the mid-diaphysis. Higher strain induced greater levels of osteoblast and osteocyte genes, whereas expression was lower in osteoclasts. Among the top differentially expressed genes at 24-hours post-loading, 17 had known functions in bone biology, of which 12 were present only in osteoblasts, 3 exclusively in osteoclasts, and 2 were present in both cell types. Based on these results, we conclude that murine tibial loading induces spatially unique transcriptomic responses correlating with strain magnitude in cortical bone. (c) 2022 American Society for Bone and Mineral Research (ASBMR).

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