Donor-matched comparison of dental pulp stem cells and bone marrow-derived mesenchymal stem cells in a rat model

被引:179
作者
Alge, Daniel L. [2 ]
Zhou, Dan [1 ]
Adams, Lyndsey L. [1 ]
Wyss, Brandon K. [1 ]
Shadday, Matthew D. [1 ]
Woods, Erik J. [4 ]
Chu, T. M. Gabriel [5 ]
Goebel, W. Scott [1 ,3 ,4 ]
机构
[1] Indiana Univ Sch Med, Herman B Wells Ctr Pediat Res, Indianapolis, IN 46202 USA
[2] Purdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47908 USA
[3] Indiana Univ Sch Med, Dept Pediat Hematol Oncol, Indianapolis, IN 46202 USA
[4] Gen BioTechnol LLC, Indianapolis, IN 46202 USA
[5] Indiana Univ, Sch Dent, Div Dent Biomat, Dept Restorat Dent, Indianapolis, IN 46202 USA
基金
美国国家卫生研究院;
关键词
dental pulp stem cells; bone marrow; mesenchymal stem cells; donor variation; proliferation; colony formation; clonogenicity; differentiation; STROMAL CELLS; IN-VITRO; CRYOPRESERVATION; DIFFERENTIATE; OSTEOBLASTS; EXPRESSION; DPSCS;
D O I
10.1002/term.220
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Dental pulp stem cells (DPSCs) have drawn much interest for the regeneration of mineralized tissues, and several studies have compared DPSCs to bone marrow-derived mesenchymal stem cells (BMMSCs). However, conflicting results, possibly due to donor-associated variability, have been published and the regenerative potential of DPSCs is currently unclear. in the present study we have sought to address this problem using a donor-matched experimental design to robustly compare the biological properties of DPSCs and BMMSCs. All experiments were performed using cells isolated from a single adult Sprague-Dawley rat. Our results show that DPSCs and BMMSCs had similar morphologies and flow cytometry profiles, were capable of forming colonies in vitro and were capable of osteogenic, chondrogenic and adipogenic differentiation. However, quantitative comparisons revealed that DPSCs had a faster population doubling time and a higher percentage of stem/progenitor cells in the population, as determined by clonogenic assays. Furthermore, while both cell populations formed mineral in vitro, DPSCs had significantly higher alkaline phosphatase activity than BMMSCs after 3 weeks in osteogenic medium. These data show several key differences between DPSCs and BMMSCs and support the possibility of using DPSCs for mineralized tissue regeneration. Copyright (C) 2009 John Wiley & Sons, Ltd.
引用
收藏
页码:73 / 81
页数:9
相关论文
共 33 条
[11]   Patterns and localization of gene expression during intramembranous bone regeneration in the rat femoral marrow ablation model [J].
Kuroda, S ;
Virdi, AS ;
Dai, Y ;
Shott, S ;
Sumner, DR .
CALCIFIED TISSUE INTERNATIONAL, 2005, 77 (04) :212-225
[12]   Species differences in growth requirements for bone marrow stromal fibroblast colony formation in vitro [J].
Kuznetsov, S ;
Robey, PG .
CALCIFIED TISSUE INTERNATIONAL, 1996, 59 (04) :265-270
[13]   An approachable human adult stem cell source for hard-tissue engineering [J].
Laino, G ;
Graziano, A ;
D'Aquino, R ;
Pirozzi, G ;
Lanza, V ;
Valiante, S ;
De Rosa, A ;
Naro, F ;
Vivarelli, E ;
Papaccio, G .
JOURNAL OF CELLULAR PHYSIOLOGY, 2006, 206 (03) :693-701
[14]   A new population of human adult dental pulp stem cells: A useful source of living autologous fibrous bone tissue (LAB) [J].
Laino, G ;
d'Aquino, R ;
Graziano, A ;
Lanza, V ;
Carinci, F ;
Naro, F ;
Pirozzi, G ;
Papaccio, G .
JOURNAL OF BONE AND MINERAL RESEARCH, 2005, 20 (08) :1394-1402
[15]   In vitro bone production using stem cells derived from human dental pulp [J].
Laino, Gregorio ;
Carinci, Francesco ;
Graziano, Antonio ;
d'Aquino, Riccardo ;
Lanza, Vladimiro ;
De Rosa, Alfredo ;
Gombos, Fernando ;
Caruso, Filippo ;
Guida, Luigi ;
Rullo, Rosario ;
Menditti, Dardo ;
Papaccio, Gianpaolo .
JOURNAL OF CRANIOFACIAL SURGERY, 2006, 17 (03) :511-515
[16]   Mesenchymal stem/progenitor cells promote the reconstitution of exogenous hematopoietic stem cells in Fancg-/- mice in vivo [J].
Li, Yan ;
Chen, Shi ;
Yuan, Jin ;
Yang, Yanzhu ;
Li, Jingling ;
Ma, Jin ;
Wu, Xiaohua ;
Freund, Marcel ;
Pollok, Karen ;
Hanenberg, Helmut ;
Goebel, W. Scott ;
Yang, Feng-Chun .
BLOOD, 2009, 113 (10) :2342-2351
[17]   The eternal tooth germ is formed at the apical end of continuously growing teeth [J].
Ohshima, H ;
Nakasone, N ;
Hashimoto, E ;
Sakai, H ;
Nakakura-Ohshima, K ;
Harada, H .
ARCHIVES OF ORAL BIOLOGY, 2005, 50 (02) :153-157
[18]   Mesenchymal progenitor cells in adult human dental pulp and their ability to form bone when transplanted into immunocompromised mice [J].
Otaki, Sayuri ;
Ueshima, Shigeru ;
Shiraishi, Kohei ;
Sugiyama, Kazuo ;
Hamada, Suguru ;
Yorimoto, Masatomo ;
Matsuo, Osamu .
CELL BIOLOGY INTERNATIONAL, 2007, 31 (10) :1191-1197
[19]   Long-term cryopreservation of dental pulp stem cells (SBP-DPSCs) and their differentiated osteoblasts: A cell source for tissue repair [J].
Papaccio, G ;
Graziano, A ;
D'Aquino, R ;
Graziano, MF ;
Pirozzi, G ;
Menditti, D ;
De Rosa, A ;
Carinci, F ;
Laino, G .
JOURNAL OF CELLULAR PHYSIOLOGY, 2006, 208 (02) :319-325
[20]   Comparative analysis of mesenchymal stem cells from bone marrow, cartilage, and adipose tissue [J].
Peng, Linyi ;
Jia, Zhuqing ;
Yin, Xinhua ;
Zhang, Xin ;
Liu, Yinan ;
Chen, Ping ;
Ma, Kangtao ;
Zhou, Chunyan .
STEM CELLS AND DEVELOPMENT, 2008, 17 (04) :761-773