A Mouse Bone Marrow Stromal Cell Line with Skeletal Stem Cell Characteristics to Study Osteogenesis In Vitro and In Vivo

被引:11
|
作者
Raeth, Sebastian [1 ]
Sacchetti, Benedetto [2 ]
Siegel, Georg [3 ]
Mau-Holzmann, Ulrike A. [4 ]
Hansmann, Jan [5 ]
Vacun, Gabriele [5 ]
Hauk, Thomas G. [1 ]
Pfizenmaier, Klaus [1 ]
Hausser, Angelika [1 ]
机构
[1] Univ Stuttgart, Inst Cell Biol & Immunol, D-70569 Stuttgart, Germany
[2] Univ Roma La Sapienza, Dept Mol Med, I-00185 Rome, Italy
[3] Univ Tubingen Hosp, Inst Clin & Expt Transfus Med IKET, Tubingen, Germany
[4] Univ Tubingen, Dept Med Genet, Tubingen, Germany
[5] Fraunhofer Inst Interfacial Engn & Biotechnol, Stuttgart, Germany
关键词
TRANSCRIPTIONAL REGULATION; MSCS SCIENCE; INBRED MICE; T-ANTIGEN; DIFFERENTIATION; DEFECTS; REPAIR; STRAINS; CULTURE; OXYGEN;
D O I
10.1089/scd.2013.0367
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Bone marrow stromal cells (BMSCs) are composed of progenitor and multipotent skeletal stem cells, which are able to differentiate in vitro into osteocytes, adipocytes, and chondrocytes. Mouse BMSCs (mBMSCs) are a versatile model system to investigate factors involved in BMSC differentiation in vitro and in vivo as a variety of transgenic mouse models are available. In this study, mBMSCs were isolated and osteogenic differentiation was investigated in tissue culture and in vivo. Three out of seven independent cell isolates showed the ability to differentiate into osteocytes, adipocytes, and chondrocytes in vitro. In vitro multipotency of an established mBMSC line was maintained over 45 passages. The osteogenic differentiation of this cell line was confirmed by quantitative polymerase chain reaction (qPCR) analysis of specific markers such as osteocalcin and shown to be Runx2 dependent. Notably, the cell line, when transplanted subcutaneously into mice, possesses full skeletal stem cell characteristics in vivo in early and late passages, evident from bone tissue formation, induction of vascularization, and hematopoiesis. This cell line provides, thus, a versatile tool to unravel the molecular mechanisms governing osteogenesis in vivo thereby aiding to improve current strategies in bone regenerative therapy.
引用
收藏
页码:1097 / 1108
页数:12
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