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Repair of bone defects with prefabricated vascularized bone grafts and double-labeled bone marrow-derived mesenchymal stem cells in a rat model.
Jiang, Xiao-Rui; Yang, Hui-Ying; Zhang, Xin-Xin; Lin, Guo-Dong; Meng, Yong-Chun; Zhang, Pei-Xun; Jiang, Shan; Zhang, Chun-Lei; Huang, Fei; Xu, Lin.
Affiliation
  • Jiang XR; Department of Orthopedics, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai 264000, P.R. China.
  • Yang HY; Department of Intensive Care Unit, Yantai Infectious Disease Hospital, Yantai 264000, P.R. China.
  • Zhang XX; Department of Orthopedics, Canner Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100000, P.R. China.
  • Lin GD; Department of Orthopedics, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai 264000, P.R. China.
  • Meng YC; Department of Orthopedics, The Affiliated Yantai Hospital of Binzhou Medical University, Yantai 264000, P.R. China.
  • Zhang PX; Department of Trauma and Orthopedics, Peking University People's Hospital, Beijing 100000, P.R. China.
  • Jiang S; Southern Medical University, Guangzhou 510515, P.R. China.
  • Zhang CL; Binzhou Medical University, Yantai 264000, P.R. China.
  • Huang F; Binzhou Medical University, Yantai 264000, P.R. China.
  • Xu L; Department of Orthopedics, The Affiliated Yantai Hospital of Binzhou Medical University, Yantai 264000, P.R. China.
Sci Rep ; 7: 39431, 2017 02 02.
Article in En | MEDLINE | ID: mdl-28150691
ABSTRACT
This study aims to investigate the repair of bone defects with prefabricated vascularized bone grafts and double-labeled bone marrow-derived mesenchymal stem cells (BMSCs) in a rat model. BMSCs were separated from rat bone marrow. LTR-CMVpro-RFP and LTR-CMVpro-GFP were transfected into the BMSCs for in vitro and in vivo tracking. BMSCs-RFP and BMSCs-GFP were induced into endothelial progenitor cells (EPCs) and osteoblasts (OBs). Rats were divided into five groups Group A in vitro prefabrication with EPCs-RFP + in vivo prefabrication with arteriovenous vascular bundle + secondary OBs-GFP implantation; Group B in vitro prefabrication with EPCs-RFP + secondary OBs-GFP implantation; Group C in vivo prefabrication with arteriovenous vascular bundle + secondary OBs-GFP implantation; Group D implantation of EPCs-RFP + implantation of with arteriovenous vascular bundle + simultaneous OBs-GFP implantation; Group E demineralized bone matrix (DBM) grafts (blank control). Among five groups, Group A had the fastest bone regeneration and repair, and the regenerated bone highly resembled normal bone tissues; Group D also had fast bone repair, but the repair was slightly slower than Group A. Therefore, in vitro prefabrication with EPCs-RFP plus in vivo prefabrication with arteriovenous vascular bundle and secondary OBs-GFP implantation could be the best treatment for bone defect.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bone Diseases / Bone Transplantation / Cell Transplantation / Mesenchymal Stem Cells Limits: Animals Language: En Journal: Sci Rep Year: 2017 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bone Diseases / Bone Transplantation / Cell Transplantation / Mesenchymal Stem Cells Limits: Animals Language: En Journal: Sci Rep Year: 2017 Document type: Article