Characteristic Change and Loss of In Vivo Osteogenic Abilities of Human Bone Marrow Stromal Cells During Passage

被引:2
作者
Agata, Hideki [1 ,2 ]
Asahina, Izumi [3 ]
Watanabe, Nobukazu [4 ]
Ishii, Yumiko [5 ]
Kubo, Noriyuki [6 ]
Ohshima, Satoshi [7 ]
Yamazaki, Mika [7 ]
Tojo, Arinobu
Kagami, Hideaki
机构
[1] Univ Tokyo, Div Mol Therapy, Inst Med Sci, Adv Clin Res Ctr,Minato Ku, Tokyo 1088639, Japan
[2] Univ Tampere, Regea Inst Regenerat Med, Tampere, Finland
[3] Nagasaki Univ, Dept Regenerat Oral Surg, Grad Sch Biomed Sci, Nagasaki 852, Japan
[4] Univ Tokyo, Lab Diagnost Med, Tokyo 1088639, Japan
[5] Univ Tokyo, FACS Core Lab, Div Stem Cell Therapy, Ctr Stem Cell Biol & Regenerat Med,Inst Med Sci, Tokyo 1088639, Japan
[6] Osaka Regenerat Med Ctr, Osaka, Japan
[7] TES Holdings Corp Ltd, Tokyo, Japan
基金
日本学术振兴会;
关键词
MESENCHYMAL STEM-CELLS; TISSUE-ENGINEERED BONE; DONOR VARIATION; DIFFERENTIATION; PERIOSTEUM; PROLIFERATION;
D O I
10.1089/ten.tea.2009.0500
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Although human bone marrow stromal cells (BMSCs) have the ability to form bone when transplanted, the responsible factors for in vivo osteogenic abilities are poorly understood. Here we report conditions that are required for human BMSCs to demonstrate their in vivo osteogenic abilities. BMSCs were obtained from healthy donors and their in vivo osteogenic abilities were analyzed. Transplantation analyses revealed that the passage number and length of osteogenic induction significantly affected ectopic bone formation. Although 2-week induction increased the percentage of success in bone formation compared with the 1-week induction, BMSCs completely lost their in vivo osteogenic ability after passage 4 regardless of the length of osteogenic induction. Despite their in vivo osteogenic ability, no significant difference was observed in alkaline phosphatase activity or gene expression of osteogenic markers between BMSCs at passages 1 and 3. Differences were only observed in in vitro mineralizing abilities. Application of basic fibroblast growth factor helped to maintain the BMSCs in vivo osteogenic ability; basic fibroblast growth factor altered cell growth and expression of HLA-DR. The results strongly suggest that there are several required conditions for human BMSCs to demonstrate their bone-forming capabilities, which should be further investigated and considered when designing a protocol for clinical bone tissue engineering.
引用
收藏
页码:663 / 673
页数:11
相关论文
共 27 条
[1]   Effective bone engineering with periosteum-derived cells [J].
Agata, H. ;
Asahina, I. ;
Yamazaki, Y. ;
Uchida, M. ;
Shinohara, Y. ;
Honda, M. J. ;
Kagami, H. ;
Ueda, M. .
JOURNAL OF DENTAL RESEARCH, 2007, 86 (01) :79-83
[2]   Effect of ischemic culture conditions on the survival and differentiation of porcine dental pulp-derived cells [J].
Agata, Hideki ;
Kagami, Hideaki ;
Watanabe, Nobukazu ;
Ueda, Minoru .
DIFFERENTIATION, 2008, 76 (09) :981-993
[3]   Primary bone-derived cells induce osteogenic differentiation without exogenous factors in human embryonic stem cells [J].
Ahn, SE ;
Kim, S ;
Park, KH ;
Moon, SH ;
Lee, HJ ;
Kim, GJ ;
Lee, YJ ;
Park, KH ;
Cha, KY ;
Chung, HM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 340 (02) :403-408
[4]   Clinical-scale expansion of a mixed population of bone marrow-derived stem and progenitor cells for potential use in bone tissue regeneration [J].
Dennis, James E. ;
Esterly, Kelly ;
Awadallah, Amad ;
Parrish, Christopher R. ;
Poynter, Gregory M. ;
Goltry, Kristin L. .
STEM CELLS, 2007, 25 (10) :2575-2582
[5]   Comparison of osteogenic ability of rat mesenchymal stem cells from bone marrow, periosteum, and adipose tissue [J].
Hayashi, Ousuke ;
Katsube, Yoshihiro ;
Hirose, Motohiro ;
Ohgushi, Hajime ;
Ito, Hiromoto .
CALCIFIED TISSUE INTERNATIONAL, 2008, 82 (03) :238-247
[6]   Molecular markers distinguish bone marrow mesenchymal stem cells from fibroblasts [J].
Ishii, M ;
Koike, C ;
Igarashi, A ;
Yamanaka, K ;
Pan, H ;
Higashi, Y ;
Kawaguchi, H ;
Sugiyama, M ;
Kamata, N ;
Iwata, T ;
Matsubara, T ;
Nakamura, K ;
Kurihara, H ;
Tsuji, K ;
Kato, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 332 (01) :297-303
[7]   Tissue-engineered approach for the treatment of steroid-induced osteonecrosis of the femoral head: Transplantation of autologous mesenchymal stem cells cultured with beta-tricalcium phosphate ceramics and free vascularized fibula [J].
Kawate, Kenji ;
Yajima, Hiroshi ;
Ohgushi, Hajime ;
Kotobuki, Noriko ;
Sugimoto, Kazuya ;
Ohmura, Tetsuji ;
Kobata, Yasunori ;
Shigematsu, Koji ;
Kawamura, Kenji ;
Tamai, Katsuya ;
Takakura, Yoshinori .
ARTIFICIAL ORGANS, 2006, 30 (12) :960-962
[8]   In vitro induction of osteogenic differentiation from non-osteogenic mesenchymal cells [J].
Lecoeur, L ;
Ouhayoun, JP .
BIOMATERIALS, 1997, 18 (14) :989-993
[9]   DEXAMETHASONE INDUCES PROLIFERATION AND TERMINAL DIFFERENTIATION OF OSTEOGENIC CELLS IN TISSUE-CULTURE [J].
MCCULLOCH, CAG ;
TENENBAUM, HC .
ANATOMICAL RECORD, 1986, 215 (04) :397-402
[10]   Bone regeneration of dental implant dehiscence defects using a cultured periosteum membrane [J].
Mizuno, Daiki ;
Kagami, Hideaki ;
Mizuno, Hirokazu ;
Mase, Junji ;
Usami, Kazutada ;
Ueda, Minoru .
CLINICAL ORAL IMPLANTS RESEARCH, 2008, 19 (03) :289-294