TY - JOUR AB - Previous evidence has suggested that physical microenvironments and mechanical stresses, independent of soluble factors, influence mesenchymal stem cell (MSC) fate. In the present study, simulated microgravity (SMG) was demonstrated to regulate the differentiation of mesenchymal stem cells. This may be a novel strategy for tissue engineering and regenerative medicine. Rat MSCs were cultured for 72 h or 10 days in either normal gravity or a clinostat to model microgravity, followed with culture in diverse differential media. A short period of stimulation (72 h) promoted MSCs to undergo endothelial, neuronal and adipogenic differentiation. In comparison, extended microgravity (10 days) promoted MSCs to differentiate into osteoblasts. A short period of exposure to SMG significantly decreased ras homolog family member A (RhoA) activity. However, RhoA activity significantly increased following prolonged exposure to SMG. When RhoA activity was inhibited, the effects of prolonged exposure to SMG were reversed. These results demonstrated that the duration of SMG regulates the differentiation fate of MSCs via the RhoA‑associated pathway. AD - Department of Urology, The Second Affiliated Hospital, Xi'an Jiaotong University, Xi'an, Shaanxi 710014, P.R. China Department of Pneumology, Traditional Chinese Medicine Hospital of Shaanxi, Xi'an, Shaanxi 710014, P.R. China Department of Encephalopathy, Traditional Chinese Medicine Hospital of Shaanxi, Xi'an, Shaanxi 710014, P.R. China AU - Xue,Li AU - Li,Yaohui AU - Chen,Jun DA - 2017/05/01 DO - 10.3892/mmr.2017.6357 EP - 3018 IS - 5 JO - Mol Med Rep KW - microgravity regeneration cytoskeletal tension differentiation PY - 2017 SN - 1791-2997 1791-3004 SP - 3011 ST - Duration of simulated microgravity affects the differentiation of mesenchymal stem cells T2 - Molecular Medicine Reports TI - Duration of simulated microgravity affects the differentiation of mesenchymal stem cells UR - https://doi.org/10.3892/mmr.2017.6357 VL - 15 ER -