The in vitro and in vivo treatment effects of overexpressed lentiviral vector-mediated human BMP2 gene in the femoral bone marrow stromal cells of osteoporotic rats

被引:5
作者
Zhao, Bing [1 ]
Wang, Qiang [1 ]
Tao, Tianzun [1 ]
Li, Juan [2 ]
Lin, Qingyuan [3 ,4 ]
机构
[1] Harbin Med Univ, Hosp 2, Dept Orthoped, Harbin 150081, Peoples R China
[2] Harbin Med Univ, Hosp 2, Dept Clin Lab Med, Harbin 150081, Peoples R China
[3] Harbin Med Univ, Dept Immunol, Harbin 150081, Peoples R China
[4] Immun & Infect Key Lab Heilongjiang Prov, Harbin 150081, Peoples R China
基金
美国国家科学基金会;
关键词
local osteoporosis; bone morphogenetic protein 2; bone marrow stromal cells; genetic infection in vitro; genetic infection in vivo; MESENCHYMAL STEM-CELLS; OSTEOGENIC DIFFERENTIATION; MORPHOGENETIC PROTEIN-2; DEFECTS; FUSION; DELIVERY; REPAIR; BMSCS;
D O I
10.3892/ijmm.2013.1507
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
This study aimed to compare the treatment effects of lentiviral vector-mediated hBMP2 which was overexpressed in the femoral bone marrow stromal cells of osteoporotic rats through genetic infection in vitro and in vivo. Comparison of the two transgenic effects may be crucial to determining the lentivirus infection method to be used. Following a comparison of the rat bone marrow stromal cells (rBMSCs) in osteoporotic (MSCs OVX) and normal (MSCs CON) groups, the lentiviral vector-mediated human bone morphogenetic protein 2 (hBMP2), which overexpressed the BMSCs of osteoporotic rats in vitro (rBMSCs in OE group), was constructed. The osteogenic ability in the overexpressed (OE) group was then compared to that of the MSCs CON. The rBMSCs in the OE group (transplants of genetic infection in vitro) and the lentivirus-containing solution (injected material of genetic infection in vivo) were injected into the femurs. The treatment effect of each group was compared via bone mineral density (BMD) and bone histomorphometry. The hBMP2-modified osteoporosis rBMSCs formed by genetic infection in vitro (n=7) had an ameliorated treatment effect on the femur as compared to that of the in vivo (n=7) (BMD: 0.315 vs. 0.19 g/cm(2), P<0.01; bone histomorphometry: For bone trabeculars (Tb.Ar/T.Ar): 0.301 vs. 0.114, P<0.01; for trabecular thickness (Tb.Th): 43.54 vs. 21.39 m, P<0.01; for trabecular separation (Tb.Sp): 115.7 vs. 304.87 m, P<0.01). The results showed that the treatment effects of osteoporotic rBMSCs on local osteoporosis performed by genetic infection were improved in vitro as compared to those in vivo.
引用
收藏
页码:1355 / 1365
页数:11
相关论文
共 41 条
[1]   BMP-2, VEGF and bFGF synergistically promote the osteogenic differentiation of rat bone marrow-derived mesenchymal stem cells [J].
Bai, Yan ;
Li, Peipei ;
Yin, Guangfu ;
Huang, Zhongbing ;
Liao, Xiaoming ;
Chen, Xianchun ;
Yao, Yadong .
BIOTECHNOLOGY LETTERS, 2013, 35 (03) :301-308
[2]   Low dose BMP-2 treatment for bone repair using a PEGylated fibrinogen hydrogel matrix [J].
Ben-David, Dror ;
Srouji, Samer ;
Shapira-Schweitzer, Keren ;
Kossover, Olga ;
Ivanir, Eran ;
Kuhn, Gisela ;
Mueller, Ralph ;
Seliktar, Dror ;
Livne, Erella .
BIOMATERIALS, 2013, 34 (12) :2902-2910
[3]   Bone marrow stromal cells (BMSCs) in bone engineering: Limitations and recent advances [J].
Derubeis, AR ;
Cancedda, R .
ANNALS OF BIOMEDICAL ENGINEERING, 2004, 32 (01) :160-165
[4]   Autogenous regulation of a network of bone morphogenetic proteins (BMPs) mediates the osteogenic differentiation in murine marrow stromal cells [J].
Edgar, Cory M. ;
Chakravarthy, Vinay ;
Barnes, George ;
Kakar, Sanjeev ;
Gerstenfeld, Louis C. ;
Einhorn, Thomas A. .
BONE, 2007, 40 (05) :1389-1398
[5]   Canonical Wnt signaling in osteoblasts is required for osteoclast differentiation [J].
Glass, Donald A., II ;
Karsenty, Gerard .
SKELETAL DEVELOPMENT AND REMODELING IN HEALTH, DISEASE, AND AGING, 2006, 1068 :117-130
[6]   Transplantation of BMSCs expressing hPDGF-A/hBD2 promotes wound healing in rats with combined radiation-wound injury [J].
Hao, L. ;
Wang, J. ;
Zou, Z. ;
Yan, G. ;
Dong, S. ;
Deng, J. ;
Ran, X. ;
Feng, Y. ;
Luo, C. ;
Wang, Y. ;
Cheng, T. .
GENE THERAPY, 2009, 16 (01) :34-42
[7]   Effects of Nicotine Administration and Nicotine Cessation on Bone Histomorphometry and Bone Biomarkers in Sprague-Dawley Male Rats [J].
Hapidin, Hermizi ;
Othman, Faizah ;
Soelaiman, Ima Nirwana ;
Shuid, Ahmad Nazrun ;
Mohamed, Norazlina .
CALCIFIED TISSUE INTERNATIONAL, 2011, 88 (01) :41-47
[8]   Lentiviral-mediated BMP-2 gene transfer enhances healing of segmental femoral defects in rats [J].
Hsu, W. K. ;
Sugiyama, O. ;
Park, S. H. ;
Conduah, A. ;
Feeley, B. T. ;
Liu, N. Q. ;
Krenek, L. ;
Virk, M. S. ;
An, D. S. ;
Chen, I. S. ;
Lieberman, J. R. .
BONE, 2007, 40 (04) :931-938
[9]   The anti-glioma effect of suicide gene therapy using BMSC expressing HSV/TK combined with overexpression of Cx43 in glioma cells [J].
Huang, Q. ;
Liu, X-Z ;
Kang, C-S ;
Wang, G-X ;
Zhong, Y. ;
Pu, P-Y .
CANCER GENE THERAPY, 2010, 17 (03) :192-202
[10]   Osteoclast differentiation in ectopic bone formation induced by recombinant human bone morphogenetic protein 2 (rhBMP-2) [J].
Irie, K ;
Alpaslan, C ;
Takahashi, K ;
Kondo, Y ;
Izumi, N ;
Sakakura, Y ;
Tsuruga, E ;
Nakajima, T ;
Ejiri, S ;
Ozawa, H ;
Yajima, T .
JOURNAL OF BONE AND MINERAL METABOLISM, 2003, 21 (06) :363-369