ZHONG Zhao-dong,ZOU Ping,YOU Yong,et al.Repairing of TBI-induced damage and remodeling of bone marrow-microvasculature by adenovirus mediated hVEGF165 gene therapy in post-BMT mice[J].Chinese Journal of Radiological Medicine and Protection,2004,24(4):316-318
Repairing of TBI-induced damage and remodeling of bone marrow-microvasculature by adenovirus mediated hVEGF165 gene therapy in post-BMT mice
Received:October 22, 2003  
DOI:
KeyWords:Vascular endothelial growth factor  Gene therapy  Total-body irradiation  Bone marrow microvasculature  Repairing
FundProject:国家自然科学基金海外青年学者基金资助项目(39928010)
Author NameAffiliationE-mail
ZHONG Zhao-dong Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China zouping@public.wh.hb.cn 
ZOU Ping Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China  
YOU Yong Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China  
刘凌波 Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China  
胡中波 Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China  
郭荣 Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China  
黄士昂   
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Abstract::
      Objective To explore the effect of vascular endothelial growth factor on the repairing of TBI- induced damage of bone marrow microvasculature in post-BMT mouse. Methods Mediated by adenovirus, hVEGF165 was expressed in TBI -conditioned BALB/c mice with syngeneic BMT. On +5 d, +10 d, +20 d, +30 d, the mice were injected with Chinese ink, following which the transparent tibias or plastic sections were used for analysis. Results hVEGF165 was successfully expressed by Ad-EGFP/hVEGF165. On +20 d, the diameter of central sinus in the VEGF group restored normally (P >0.05) and the percentage of microvasculature surface area returned to normal level (P >0.05). The percent cellularity of BM in the VEGF group began to be higher than that of other groups after +20 d (P <0.05). Conclusion The expression of hVEGF165 promotes the repairing of TBI -induced damage and the remodeling of bone marrow microvasculature, the resulting in rapid hematopoietic reconstruction.
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