Human umbilical cord and dental pulp-derived mesenchymal stem cells: Biological characteristics and potential roles in vitro and in vivo

被引:10
作者
Cui, Xiaoyan [1 ]
Chen, Lei [2 ]
Xue, Ting [1 ]
Yu, Jing [1 ]
Liu, Jie [1 ]
Ji, Yazhong [3 ]
Cheng, Liming [2 ]
机构
[1] Tongji Univ, Sch Med, Translat Ctr Stem Cell Res, Shanghai 200065, Peoples R China
[2] Tongji Univ, Sch Med, Dept Spine Surg, Tongji Hosp, Shanghai 200065, Peoples R China
[3] Tongji Univ, Sch Med, Dept Reprod Med, Tongji Hosp, Shanghai 200065, Peoples R China
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
human umbilical cord-derived mesenchymal stem cells; survivin; dental pulp-derived stem cells; differentiation; RNA sequencing; NEURON-LIKE CELLS; STROMAL CELLS; BONE-MARROW; SPINAL-CORD; RNA-SEQ; THERAPY; TRANSPLANTATION; TISSUES; TOPHAT; GENE;
D O I
10.3892/mmr.2015.3198
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mesenchymal stem/stromal cells (MSCs) have a wide application in cell-based therapies and tissue engineering. In the present study, the differentiation, survivin (SVV)-modified effects and molecular basis of human umbilical cord-derived MSCs (HUMSCs) and dental pulp-derived stem cells (DPSCs) were investigated. The HUMSCs were found to differentiate into adipocytes more readily than the DPSCs and the HUMSCs and DPSCs were each able to differentiate into osteoblasts and chondroblasts. Following modification of the MSCs by SVV, the secretion of SVV in the modified HUMSCs was significantly higher compared with that in the modified DPSCs. In vivo, survival of the SVV-modified DPSCs was observed at 4 and 14 days after intrastriatal transplantation, as was the expression of SVV and differentiation into astrocytes. The gene expression profiles of the control and modified HUMSCs and DPSCs were compared using RNA sequencing and an association was observed between gene expression and variability in cell line function. These findings provide novel information regarding the differences between HUMSCs and DPSCs and insight into optimal cell sources for therapeutic applications.
引用
收藏
页码:3269 / 3278
页数:10
相关论文
共 25 条
[1]   Mesenchymal stem cells from the Wharton's jelly of umbilical cord segments provide stromal support for the maintenance of cord blood hematopoietic stem cells during long-term ex vivo culture [J].
Bakhshi, Tiki ;
Zabriskie, Ryan C. ;
Bodie, Shamanique ;
Kidd, Shannon ;
Ramin, Susan ;
Paganessi, Laura A. ;
Gregory, Stephanie A. ;
Fung, Henry C. ;
Christopherson, Kent W., III .
TRANSFUSION, 2008, 48 (12) :2638-2644
[2]   Mesenchymal Stromal Cells: A New Tool against Graft-versus-Host Disease? [J].
Baron, Frederic ;
Storb, Rainer .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2012, 18 (06) :822-840
[3]   Cytoprotective Signaling Associated with Nitric Oxide Upregulation in Tumor Cells Subjected to Photodynamic Therapy-like Oxidative Stress [J].
Bhowmick, Reshma ;
Girotti, Albert W. .
FREE RADICAL BIOLOGY AND MEDICINE, 2013, 57 :39-48
[4]   Generating neuron-like cells from BM-derived mesenchymal stromal cells in vitro [J].
Choong, P-F ;
Mok, P-L ;
Cheong, S-K ;
Leong, C-F ;
Then, K-Y .
CYTOTHERAPY, 2007, 9 (02) :170-183
[5]   Genetic modification of mesenchymal stem cells in spinal cord injury repair strategies [J].
Cui, Xiaoyan ;
Chen, Lei ;
Ren, Yilong ;
Ji, Yazhong ;
Liu, Wei ;
Liu, Jie ;
Yan, Qiao ;
Cheng, Liming ;
Sun, Yi E. .
BIOSCIENCE TRENDS, 2013, 7 (05) :202-208
[6]   The effects of cryopreservation on cells isolated from adipose, bone marrow and dental pulp tissues [J].
Davies, O. G. ;
Smith, A. J. ;
Cooper, P. R. ;
Shelton, R. M. ;
Scheven, B. A. .
CRYOBIOLOGY, 2014, 69 (02) :342-347
[7]   Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement [J].
Dominici, M. ;
Le Blanc, K. ;
Mueller, I. ;
Slaper-Cortenbach, I. ;
Marini, F. C. ;
Krause, D. S. ;
Deans, R. J. ;
Keating, A. ;
Prockop, D. J. ;
Horwitz, E. M. .
CYTOTHERAPY, 2006, 8 (04) :315-317
[8]   Transplantation of umbilical cord-derived mesenchymal stem cells into the striata of R6/2 mice: behavioral and neuropathological analysis [J].
Fink, Kyle D. ;
Rossignol, Julien ;
Crane, Andrew T. ;
Davis, Kendra K. ;
Bombard, Matthew C. ;
Bavar, Angela M. ;
Clerc, Steven ;
Lowrance, Steven A. ;
Song, Cheng ;
Lescaudron, Laurent ;
Dunbar, Gary L. .
STEM CELL RESEARCH & THERAPY, 2013, 4
[9]   The antiapoptosis protein survivin is associated with cell cycle entry of normal cord blood CD34+ cells and modulates cell cycle and proliferation of mouse hematopoietic progenitor cells [J].
Fukuda, S ;
Foster, RG ;
Porter, SB ;
Pelus, LM .
BLOOD, 2002, 100 (07) :2463-2471
[10]   Postnatal human dental pulp stem cells (DPSCs) in vitro and in vivo [J].
Gronthos, S ;
Mankani, M ;
Brahim, J ;
Robey, PG ;
Shi, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (25) :13625-13630