The role of bone marrow-derived mesenchymal stem cells in treating formocresol induced oral ulcers in dogs

被引:31
作者
El-Menoufy, H. [2 ,3 ]
Aly, L. A. A. [1 ]
Aziz, M. T. A. [4 ]
Atta, H. M. [4 ]
Roshdy, N. K. [4 ]
Rashed, L. A. [4 ]
Sabry, D. [4 ]
机构
[1] Future Univ, Fac Dent, Cairo, Egypt
[2] Misr Univ Sci & Technol, Fac Dent, Dept Periodontol, Cairo, Egypt
[3] Misr Univ Sci & Technol, Fac Dent, Dept Oral Med & Oral Diag, Cairo, Egypt
[4] Cairo Univ, Fac Med, Cairo, Egypt
关键词
bone marrow; mesenchymal stem cells; oral ulcer; ENDOTHELIAL GROWTH-FACTOR; MOLECULAR-MECHANISMS; EXPRESSION; INDUCTION; REPAIR;
D O I
10.1111/j.1600-0714.2009.00819.x
中图分类号
R78 [口腔科学];
学科分类号
100302 [口腔临床医学];
摘要
Background: Mesenchymal stem cells (MSCs), a subpopulation of adult somatic stem cells, are an attractive stem cell source in regenerative medicine because of their multipotentiality. In this study, the effects of MSCs transplantation on oral ulcer healing were examined. Methods: Mesenchymal stem cells were isolated from bone marrow aspirates of dogs by dish adherence and expanded in culture. Oral ulcers were induced by topical application of formocresol in the oral cavity of dogs. Either autologous MSCs or vehicle (saline) was injected around the ulcer. The healing process of the ulcer was monitored clinically and histopathologically. Gene expression of vascular endothelial growth factor (VEGF) was detected in MSCs by reverse transcription-polymerase chain reaction. Expression of VEGF and collagen genes was detected in biopsies from all ulcers. Results: Mesenchymal stem cells expressed mRNA for VEGF MSCs transplantation significantly accelerated oral ulcer healing compared with controls. There was increased expression of both collagen and VEGF genes in MSCs-treated ulcers compared with controls. Conclusion: Mesenchymal stem cells transplantation may help accelerate oral ulcer healing, possibly through the induction of angiogenesis by VEGF together with increased intracellular matrix formation as detected by increased collagen gene expression.
引用
收藏
页码:281 / 289
页数:9
相关论文
共 42 条
[1]
SCARLESS FETAL HEALING - THERAPEUTIC IMPLICATIONS [J].
ADZICK, NS ;
LONGAKER, MT .
ANNALS OF SURGERY, 1992, 215 (01) :3-7
[2]
ANATERESA S, 2008, BRAZ DENT J, V19, P33
[3]
Colonic subepithelial myofibroblasts in mucosal inflammation and repair: contribution of bone marrow-derived stem cells to the gut regenerative response [J].
Andoh, A ;
Bamba, S ;
Fujiyama, Y ;
Brittan, M ;
Wright, NA .
JOURNAL OF GASTROENTEROLOGY, 2005, 40 (12) :1089-1099
[4]
Aziz MTA, 2008, MED SCI MONITOR, V14, pBR249
[5]
BASSON MD, 1993, EUR J GASTROEN HEPAT, V5, pS21
[6]
In vitro evidence for matrix regulation of intestinal epithelial biology during mucosal healing [J].
Basson, MD .
LIFE SCIENCES, 2001, 69 (25-26) :3005-3018
[7]
SYSTEMIC DISTRIBUTION OF [C-14]-LABELED PARAFORMALDEHYDE INCORPORATED WITHIN FORMOCRESOL FOLLOWING PULPOTOMIES IN DOGS [J].
BLOCK, RM ;
LEWIS, RD ;
HIRSCH, J ;
COFFEY, J ;
LANGELAND, K .
JOURNAL OF ENDODONTICS, 1983, 9 (05) :176-189
[8]
BOEVE C, 1982, J DENT CHILD, V49, P191
[9]
A regenerative role for bone marrow following experimental colitis: Contribution to neovasculogenesis and myofibroblasts [J].
Brittan, M ;
Chance, V ;
Elia, G ;
Poulsom, R ;
Alison, MR ;
MacDonald, TT ;
Wright, NA .
GASTROENTEROLOGY, 2005, 128 (07) :1984-1995
[10]
MESENCHYMAL STEM-CELLS [J].
CAPLAN, AI .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1991, 9 (05) :641-650