Regeneration of periodontal tissues using allogeneic periodontal ligament stem cells in an ovine model

被引:87
作者
Mrozik, Krzysztof Marek [1 ,2 ]
Wada, Naohisa [1 ,3 ]
Marino, Victor [1 ]
Richter, Ward [4 ]
Shi, Songtao [5 ]
Wheeler, Donna L. [6 ]
Gronthos, Stan [2 ,7 ]
Bartold, P. Mark [1 ]
机构
[1] Univ Adelaide, Colgate Australian Clin Dent Res Ctr, Sch Dent, Adelaide, SA, Australia
[2] Univ Adelaide, Sch Med Sci, Mesenchymal Stem Cell Lab, Adelaide, SA, Australia
[3] Kyushu Univ, Fac Dent Sci, Div Oral Rehabil, Dept Endodontol & Operat Dent, Fukuoka 812, Japan
[4] Druquest Int Inc, Leeds, AL USA
[5] Univ So Calif, Ctr Craniofacial Mol Biol, Los Angeles, CA USA
[6] BioSolut Consulting LLC, Provincetown, MA USA
[7] Univ Adelaide, Ctr Stem Cell Res, Robinson Inst, Adelaide, SA, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
allogeneic; alveolar bone; cementum; periodontal ligament stem cells; regeneration; Sharpey"s fibers; MARROW STROMAL CELLS; IN-VIVO; DEFECT MODEL; BONE; MATRIX; RESPONSES; THERAPY; INHIBIT; REPAIR; SHEEP;
D O I
10.2217/rme.13.66
中图分类号
Q813 [细胞工程];
学科分类号
100113 [医学细胞生物学];
摘要
Aim: To investigate the capacity of allogeneic periodontal ligament stem cells (PDLSCs) to regenerate periodontal tissues using an ovine periodontal defect model. Materials & methods: Surgically created zero-wall dehiscence periodontal defects created in Merino sheep were filled with 1 x 10(7) allogeneic PDLSCs attached to Gelfoam((R)), Gelfoam alone or left untreated. After 4 weeks, histological analysis was performed to assess periodontal regeneration. Results: Allogeneic PDLSCs were well tolerated by recipient animals. The mean area of new alveolar bone was significantly greater in the PDLSC + Gelfoam treatment group compared with the defect-alone group. The PDLSC + Gelfoam and Gelfoam-only treatment groups displayed significantly greater length of new cementum and percentage of cementum regrowth compared with the defect-alone group. New Sharpeys fibers were generally more organized and significantly thicker within the PDLSC + Gelfoam treatment group. The PDLSC + Gelfoam treatment group also showed a trend of increased Sharpeys fiber attachment length compared with the Gelfoam-only and defect-alone groups. Conclusion: These studies support the potential use of allogeneic PDLSC preparations as viable therapies for periodontal regeneration in the clinical setting.
引用
收藏
页码:711 / 723
页数:13
相关论文
共 55 条
[1]
Human mesenchymal stem cells modulate allogeneic immune cell responses [J].
Aggarwal, S ;
Pittenger, MF .
BLOOD, 2005, 105 (04) :1815-1822
[2]
Implanted Adult Human Dental Pulp Stem Cells Induce Endogenous Axon Guidance [J].
Arthur, Agnieszka ;
Shi, Songtao ;
Zannettino, Andrew C. W. ;
Fujii, Nobutaka ;
Gronthos, Stan ;
Koblar, Simon A. .
STEM CELLS, 2009, 27 (09) :2229-2237
[3]
Mesenchymal stem cells suppress lymphocyte proliferation in vitro and prolong skin graft survival in vivo [J].
Bartholomew, A ;
Sturgeon, C ;
Siatskas, M ;
Ferrer, K ;
McIntosh, K ;
Patil, S ;
Hardy, W ;
Devine, S ;
Ucker, D ;
Deans, R ;
Moseley, A ;
Hoffman, R .
EXPERIMENTAL HEMATOLOGY, 2002, 30 (01) :42-48
[4]
Bartold P., 1998, BIOL PERIODONTAL CON
[5]
Stem cells and periodontal regeneration [J].
Bartold, PM ;
Shi, ST ;
Gronthos, S .
PERIODONTOLOGY 2000, 2006, 40 :164-172
[6]
Tissue engineering: a new paradigm for periodontal regeneration based on molecular and cell biology [J].
Bartold, PM ;
McCulloch, CAG ;
Narayanan, AS ;
Pitaru, S .
PERIODONTOLOGY 2000, 2000, 24 :253-269
[7]
UNTREATED PERIODONTAL-DISEASE - LONGITUDINAL-STUDY [J].
BECKER, W ;
BERG, L ;
BECKER, BE .
JOURNAL OF PERIODONTOLOGY, 1979, 50 (05) :234-244
[8]
Effect of decalcified freeze-dried bone allograft on the healing of jaw defects after cyst enucleation [J].
Bodner, L .
JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 1996, 54 (11) :1282-1286
[9]
A comparison of 2 polytetrafluoroethylene membranes in guided tissue regeneration in sheep [J].
DaneshMeyer, MJ ;
Pack, ARC ;
McMillan, MD .
JOURNAL OF PERIODONTAL RESEARCH, 1997, 32 (01) :20-30
[10]
Human bone marrow stromal cells suppress T-lymphocyte proliferation induced by cellular or nonspecific mitogenic stimuli [J].
Di Nicola, M ;
Carlo-Stella, C ;
Magni, M ;
Milanesi, M ;
Longoni, PD ;
Matteucci, P ;
Grisanti, S ;
Gianni, AM .
BLOOD, 2002, 99 (10) :3838-3843