Mechanical unloading of bone in microgravity reduces mesenchymal and hematopoietic stem cell-mediated tissue regeneration

• Published in: Stem cell research 2014-09, Vol.13 (2), p.181-201
• Main Authors: Blaber, E.A., Dvorochkin, N., Torres, M.L., Yousuf, R., Burns, B.P., Globus, R.K., Almeida, E.A.C.
• Format: Article
• Language: English
• Subjects: Animals; Biomarkers - metabolism; Biomechanical Phenomena; Bone Regeneration; Bone Resorption - genetics; Bone Resorption - metabolism; Bone Resorption - pathology; Bone Resorption - physiopathology; Cell Differentiation; Cells, Cultured; Female; Femur Head - metabolism; Femur Head - pathology; Femur Head - physiopathology; Gene Expression Regulation, Developmental; Hematopoietic Stem Cells - metabolism; Hematopoietic Stem Cells - pathology; Mesenchymal Stromal Cells - metabolism; Mesenchymal Stromal Cells - pathology; Mice, Inbred C57BL; Osteoclasts - metabolism; Osteoclasts - pathology; Phenotype; Regenerative Medicine - methods; Stress, Mechanical; Time Factors; Tissue Engineering; Weight-Bearing; Weightlessness Simulation
• ISSN: 1873-5061; 1876-7753
• DOI: 10.1016/j.scr.2014.05.005

Mechanical loading of mammalian tissues is a potent promoter of tissue growth and regeneration, whilst unloading in microgravity can cause reduced tissue regeneration, possibly through effects on stem cell tissue progenitors. To test the specific hypothesis that mechanical unloading alters differentiation of bone marrow mesenchymal and hematopoietic stem cell lineages, we studied cellular and molecular aspects of how bone marrow in the mouse proximal femur responds to unloading in microgravity. Trabecular and cortical endosteal bone surfaces in the femoral head underwent significant bone resorption in microgravity, enlarging the marrow cavity. Cells isolated from the femoral head marrow compartment showed significant down-regulation of gene expression markers for early mesenchymal and hematopoietic differentiation, including FUT1(−6.72), CSF2(−3.30), CD90(−3.33), PTPRC(−2.79), and GDF15(−2.45), but not stem cell markers, such as SOX2. At the cellular level, in situ histological analysis revealed decreased megakaryocyte numbers whilst erythrocytes were increased 2.33 fold. Furthermore, erythrocytes displayed elevated fucosylation and clustering adjacent to sinuses forming the marrow–blood barrier, possibly providing a mechanistic basis for explaining spaceflight anemia. Culture of isolated bone marrow cells immediately after microgravity exposure increased the marrow progenitor's potential for mesenchymal differentiation into in-vitro mineralized bone nodules, and hematopoietic differentiation into osteoclasts, suggesting an accumulation of undifferentiated progenitors during exposure to microgravity. These results support the idea that mechanical unloading of mammalian tissues in microgravity is a strong inhibitor of tissue growth and regeneration mechanisms, acting at the level of early mesenchymal and hematopoietic stem cell differentiation. •Unloading in microgravity causes femoral bone degeneration.•Microgravity suppresses hematopoietic and mesenchymal early differentiation genes.•Differentiation potential of bone marrow stem cells is increased upon reloading.•Unloading in microgravity blocks exit of mature erythrocytes into the blood stream.•Mechanical unloading is a strong inhibitor of tissue regeneration.