Menu 
  • Home
  • Research on Station
        • Benefits of Research on the ISS
        • Industrial R&D
        • Current Project Pipeline
        • Researcher Interviews
      • Current RFI

        hardware

        RFI-Organs-On-Chips Research

      • Researcher Interviews

        No items found
  • Getting to Space
        • Getting to Space
        • Implementation Partners
        • ISS Hardware
        • Proposal Submission Process
        • Launch Vehicles
        • Support Services
      • Recent Posts

        No items found
      • Projects in Flight

        • Materials Testing – Earth Abundant Textured Thin Film Photovoltaics
        • GLASS AIS TransponderGlobal AIS on Space Station (GLASS)
        • MultiLab: Research Server for the ISS
        • Story Time from Space – 2
        • NIH-Osteo
        View Current ISS Project Pipeline »
  • Research Library
        • ISS National Lab Research Database
        • ISS National Lab Reports
        • Web Resources
        • Research Apps
      • Recently Added Research

        • Genotype, B-vitamin status, and androgens affect spaceflight-induced ophthalmic changes
        • SUBSONIC MOTION OF A PROJECTILE IN A FLUID COMPLEX PLASMA UNDER MICROGRAVITY CONDITIONS
        • Coactivator-Dependent Oscillation of Chromatin Accessibility Dictates Circadian Gene Amplitude via REV-ERB Loading
      • Popular Tags

        • Cell Differentiation
        • Earth Observation
        • Fluid physics
        • Gene Expression
        • Human Research
        • Material science
        • Mice
        • Microbiology
        • Simulated microgravity
        • Technology demonstration
  • Make Contact
  • Home
  • Research on Station
    • Benefits of Microgravity
    • Industrial R&D
    • Current Project Pipeline
    • Research Opportunities
    • Researcher Interviews
  • Facilities & Hardware
    • ISS Hardware
    • Implementation Partners
  • Getting to Space
    • Getting to Space
    • Proposal Submission Process
    • Launch Vehicles
  • Research Library
    • Research Apps
    • Researcher Guides
    • Resources
    • Publication Database

« Go Back

Impaired osteoblastogenesis potential of progenitor cells in skeletal unloading is associated with alterations in angiogenic and energy metabolism profile

Vandamme, K., et al. (2012). "Impaired osteoblastogenesis potential of progenitor cells in skeletal unloading is associated with alterations in angiogenic and energy metabolism profile." Bio-Medical Materials and Engineering 22 4: 219-226

Skeletal unloading provokes bone loss. These bone alterations have been shown to be associated with impairment of osteoblastic activity. In the present study, we evaluated the effect of skeletal unloading on bone marrow progenitor cells, for exploration of the underlying mechanism. Wistar rats were randomized to be either hindlimb unloaded for 9 days or to act as controls. Micro-CT was used to detect tibial trabecular architecture changes in response to skeletal unloading. Microgravity conditions for 9 days resulted in a decreased number and an increased spacing of the bone trabeculae in the proximal tibia. The proliferative capacity of the femoral bone marrow samples was assessed (fibroblast-colony-forming assay). By using qPCR, the expression of selected markers of vascularization (Vegfa; Hif1a; Angpt1), energy metabolism (Prkaa2; Mtor), bone formation (Runx2; Alp; Bglap; Bmp2; Bmp4; Bmp7) and bone resorption (Acp5; Tnfsf11; Tnfrsf11b) in these bone marrow suspensions was measured. We demonstrated a striking decrease in the number of fibroblastic progenitors in response to hindlimb unloading. This deficit in proliferation was shown to be accompanied by altered hindlimb perfusion and cellular energy homeostasis. Ex vivo culture assays of the bone marrow-derived progenitor cells screened for osteogenic (Runx2; Alp; Bglap) and adipogenic (Pparg; Fabp4) differentiation alterations in response to microgravity. Induced progenitor cells from unloaded rats showed a delay in osteogenic differentiation and impaired adipogenic differentiation compared to control. The data of this multi-level approach demonstrate that skeletal unloading significantly affects the bone tissue and its metabolism at the progenitor stage. The molecular expressions of the bone marrow population support a role of cellular metabolic stresses in skeletal alterations induced by inactivity.

Related URLs:
<Go to ISI>://WOS:000306372100004

ISSN: 0959-2989

DOI: 10.3233/bme-2012-0711

Accession Number: WOS:000306372100004

Share this
0
0
0
Tags: *Gene Expression Regulation, Animals, Bone Marrow Cells/*cytology/metabolism, Cell Differentiation, Energy Metabolism, Female, Hindlimb Suspension, Neovascularization, Osteoblasts/cytology, Osteogenesis, Physiologic, Rats, Stem Cells/cytology/*metabolism, Wistar