Characterization and Biodistribution of Human Mesenchymal Stem Cells Transduced with Lentiviral-mediated BMP2

被引:9
|
作者
Choi, Kyoung Suk [1 ]
Ahn, Soon Young [1 ]
Kim, Tek Seung [1 ]
Kim, Jiseon [2 ]
Kim, Byoung-Guk [1 ]
Han, Kyung Ho [1 ]
Ban, Sang Ja [1 ]
Kim, Hyung Soo [1 ]
Choi, Youngju [3 ]
Lim, Chul-Joo [1 ]
机构
[1] Natl Inst Food & Drug Safety Evaluat, Dept Pharmaceut & Med Devices Res, Korea Food & Drug Adm, Seoul 122704, South Korea
[2] Natl Inst Toxicol Res, Dept Pharmacol Res, Korea Food & Drug Adm, Seoul 122704, South Korea
[3] Natl Inst Food & Drug Safety Evaluat, Res Planning & Management Div, Korea Food & Drug Adm, Seoul 122704, South Korea
关键词
MSCs; BMP2; Characterization; Lentivirus; BONE MORPHOGENETIC PROTEIN-2; FORMATION IN-VIVO; GENE-TRANSFER; OSTEOBLASTIC DIFFERENTIATION; STROMAL CELLS; VITRO; EXPRESSION; VECTORS; THERAPY;
D O I
10.1007/s12272-011-0410-y
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Recently, the genetic modification of mesenchymal stem cells (MSCs) has led to increased differentiation potential. For the therapeutic application of genetically modified MSCs, it is crucial to evaluate their characteristics and safety. In this study, we investigated the effects of bone morphogenetic protein 2 (BMP2) gene transfer on the characteristics and biodistribution of human MSCs. Lentiviral-mediated BMP2 transduction to MSCs enhanced osteocyte differentiation and decreased adipocyte differentiation. Although there is no significant difference in cell proliferation capacity, MSCs transduced BMP2 proliferate somewhat higher than nontransduced or GFP transduced MSCs. No significant changes were observed in surface antigen expression in genetically modified MSCs. In vivo transplantation of lentiviral-mediated BMP2 gene transferred MSCs to nude mice did not result in tumor formation. To evaluate the biodistribution of genetically modified cells, MSCs carrying BMP2 were injected into the tail vein of femur fractured mice. The introduced MSCs were detected in the spleen, testis and fractured femur 28 days post-implantation. These findings suggest that diverse safety tests for genetically modified MSCs should be considered, particularly when a lentivirus mediated gene transfer method is used.
引用
收藏
页码:599 / 606
页数:8
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