Isolation and characterization of stem cells derived from human third molar tooth germs of young adults: implications in neo-vascularization, osteo-, adipo- and neurogenesis

被引:102
作者
Yalvac, M. E. [2 ]
Ramazanoglu, M. [3 ]
Rizvanov, A. A. [1 ,2 ,4 ]
Sahin, F. [2 ]
Bayrak, O. F. [2 ]
Salli, U. [5 ]
Palotas, A. [6 ]
Kose, G. T. [2 ]
机构
[1] Kazan VI Lenin State Univ, Fac Biol & Soil Sci, Dept Genet, R-420008 Kazan, Russia
[2] Yeditepe Univ, Coll Engn & Architecture, Dept Genet & BioEngn, Istanbul, Turkey
[3] Istanbul Univ, Coll Dent, Dept Oral Surg, Istanbul, Turkey
[4] Kazan State Med Univ, Core Res Lab, Kazan, Russia
[5] Penn State Univ, Coll Med, Dept Pharmacol, Hershey, PA USA
[6] Asklepios Med Bt Private Practice & Res Ctr, Szeged, Hungary
基金
俄罗斯基础研究基金会;
关键词
germ; molar; stem cell; tooth; transcription factor; DENTAL FOLLICLE CELLS; BONE-MARROW; GENE-EXPRESSION; IN-VIVO; TISSUE; LINES; DIFFERENTIATION; PLURIPOTENCY; REGENERATION; PROGENITORS;
D O I
10.1038/tpj.2009.40
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A number of studies have reported in the last decade that human tooth germs contain multipotent cells that give rise to dental and peri-odontal structures. The dental pulp, third molars in particular, have been shown to be a significant stem cell source. In this study, we isolated and characterized human tooth germ stem cells (hTGSCs) from third molars and assessed the expression of developmentally important transcription factors, such as oct4, sox2, klf4, nanog and c-myc, to determine their pluri-potency. Flow-cytometry analysis revealed that hTGSCs were positive for CD73, CD90, CD105 and CD166, but negative for CD34, CD45 and CD133, suggesting that these cells are mesenchymal-like stem cells. Under specific culture conditions, hTGSCs differentiated into osteogenic, adipogenic and neurogenic cells, as well as formed tube-like structures in Matrigel assay. hTGSCs showed significant levels of expression of sox2 and c-myc messenger RNA (mRNA), and a very high level of expression of klf4 mRNA when compared with human embryonic stem cells. This study reports for the first time that hTGSCs express developmentally important transcription factors that could render hTGSCs an attractive candidate for future somatic cell re-programming studies to differentiate germs into various tissue types, such as neurons and vascular structures. In addition, these multipotential hTGSCs could be important stem cell sources for autologous transplantation. The Pharmacogenomics Journal (2010) 10, 105-113; doi:10.1038/tpj.2009.40; published online 1 September 2009
引用
收藏
页码:105 / 113
页数:9
相关论文
共 45 条
[1]   Hypoxia promotes murine bone-marrow-derived stromal cell migration and tube formation [J].
Annabi, B ;
Lee, YT ;
Turcotte, S ;
Naud, E ;
Desrosiers, RR ;
Champagne, M ;
Eliopoulos, N ;
Galipeau, J ;
Béliveau, R .
STEM CELLS, 2003, 21 (03) :337-347
[2]   Are cementoblasts a subpopulation of osteoblasts or a unique phenotype? [J].
Bosshardt, DD .
JOURNAL OF DENTAL RESEARCH, 2005, 84 (05) :390-406
[3]   Identification of mesenchymal stem/progenitor cells in human first-trimester fetal blood, liver, and bone marrow [J].
Campagnoli, C ;
Roberts, IAG ;
Kumar, S ;
Bennett, PR ;
Bellantuono, I ;
Fisk, NM .
BLOOD, 2001, 98 (08) :2396-2402
[4]   Dental pulp stem cells: A promising tool for bone regeneration [J].
d'Aquino, Riccardo ;
Papaccio, Gianpaolo ;
Laino, Gregorio ;
Graziano, Antonio .
STEM CELL REVIEWS, 2008, 4 (01) :21-26
[5]  
De Bari C, 2001, ARTHRITIS RHEUM-US, V44, P1928, DOI 10.1002/1529-0131(200108)44:8<1928::AID-ART331>3.0.CO
[6]  
2-P
[7]   Muscle regeneration by bone marrow derived myogenic progenitors [J].
Ferrari, G ;
Cusella-De Angelis, G ;
Coletta, M ;
Paolucci, E ;
Stornaiuolo, A ;
Cossu, G ;
Mavilio, F .
SCIENCE, 1998, 279 (5356) :1528-1530
[8]   Mammalian neural stem cells [J].
Gage, FH .
SCIENCE, 2000, 287 (5457) :1433-1438
[9]   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
[10]   In vivo derivation of glucose-competent pancreatic endocrine cells from bone marrow without evidence of cell fusion [J].
Ianus, A ;
Holz, GG ;
Theise, ND ;
Hussain, MA .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (06) :843-850