摘要
Yong Tang a,d,e,2,Keyu Luo a,c,2,Yin Chen d,2,Yueqi Chen a,b,Rui Zhou a,Can Chen a,Jiulin Tan a,Moyuan Deng a,Qijie Dai a,Xueke Yu a,Jian Liu a,Chengmin Zhang a,Wenjie Wu a,Jianzhong Xu a,**,1,Shiwu Dong a,b,***,1,Fei Luo a,*,1 a National&Regional United Engineering Lab of Tissue Engineering,Department of Orthopedics,Southwest Hospital,Third Military Medical University,Chongqing,China b Department of Biomedical Materials Science,Third Military Medical University,Chongqing,China c Department of Spine Surgery,Center for Orthopedics,Daping Hospital,Third Military Medical University,Chongqing,China d State Key Laboratory of Trauma,Burns and Combined Injury,Institute of Combined Injury,Chongqing Engineering Research Center for Nanomedicine,College of Preventive Medicine,Third Military Medical University,Chongqing,China e Department of Orthopaedics,72nd Group Army Hospital,Huzhou University,Huzhou,Zhejiang,China The authors regret that the published version of the above article contained several errors which were not identified during the proofing stage.Also,figures 2D,3A and 5A have been replaced.The authors apologize for these errors and state that these corrections do not change the scientific conclusions of the article in any way.Fig.2.(D)High-resolution laser scanning confocal microscopy images of the cytoskeleton(red,phalloidin)and nuclei(blue,DAPI),showing MSCs cultured on identified scaffold struts for 1,4 and 7 days.Scale bar,100μm.Fig.3.(A)Transwell assays for the migration of MSCs using 152RM(n=5 each).Representative crystal violet staining images are shown in the left panel.Quantification of cell migration is shown in the right panel.Scale bar,100μm.
