AIM: To identify and compare the expression level of growth-factor-associated genes in human periodontal ligament (PDL) stem cells with dental pulp stem cells isolated from deciduous teeth as well as to assess their suitability in regenerative dentistry. METHODOLOGY: Periodontal ligament and dental pulp stem cells were isolated from deciduous teeth. Human both cells lines were expanded in identical culture condition, and their differentiation profile and cell surface antigen were compared. In addition, growth factor associated genes profiles were assessed using PCR array. RESULTS: Stem cells from deciduous dental pulp (SCD) and periodontal ligament cultures were capable of proliferating and mutually expressed the specific phenotype profile of human mesenchymal stem cells (MSCs). In osteogenic cultures, calcium nodules were observed by day 21 in PDL and dental pulp stem cells. In adipogenic cultures, both cell populations showed positive Oil Red O staining by day 21. Likewise, in chondrogenic cultures, both stem cells expressed the formation of proteoglycan. Interestingly, the expression of growth factor analysis revealed a higher propensity of PDL stem cells towards angiogenesis, osteogenesis and neurogenesis as compared to dental pulp stem cells. CONCLUSIONS: The data suggest the PDL stem cell population can be utilized as potential sources for cell-based therapies in regenerative dentistry.
AIM: To identify and compare the expression level of growth-factor-associated genes in human periodontal ligament (PDL) stem cells with dental pulp stem cells isolated from deciduous teeth as well as to assess their suitability in regenerative dentistry. METHODOLOGY: Periodontal ligament and dental pulp stem cells were isolated from deciduous teeth. Human both cells lines were expanded in identical culture condition, and their differentiation profile and cell surface antigen were compared. In addition, growth factor associated genes profiles were assessed using PCR array. RESULTS: Stem cells from deciduous dental pulp (SCD) and periodontal ligament cultures were capable of proliferating and mutually expressed the specific phenotype profile of human mesenchymal stem cells (MSCs). In osteogenic cultures, calcium nodules were observed by day 21 in PDL and dental pulp stem cells. In adipogenic cultures, both cell populations showed positive Oil Red O staining by day 21. Likewise, in chondrogenic cultures, both stem cells expressed the formation of proteoglycan. Interestingly, the expression of growth factor analysis revealed a higher propensity of PDL stem cells towards angiogenesis, osteogenesis and neurogenesis as compared to dental pulp stem cells. CONCLUSIONS: The data suggest the PDL stem cell population can be utilized as potential sources for cell-based therapies in regenerative dentistry.
Authors: Jessica Ratajczak; Annelies Bronckaers; Yörg Dillen; Pascal Gervois; Tim Vangansewinkel; Ronald B Driesen; Esther Wolfs; Ivo Lambrichts; Petra Hilkens Journal: Stem Cells Int Date: 2016-09-05 Impact factor: 5.443