Mesenchymal stem cells derived from inflamed dental pulpal and gingival tissue: a potential application for bone formation

Abstract Background Chronic periodontal disease is an infectious disease consisting of prolonged inflammation of the supporting tooth tissue and resulting in bone loss. Guided bone regeneration procedures have become common and safe treatments in dentistry, and in this context dental stem cells woul...

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Main Authors: Laura Tomasello, Rodolfo Mauceri, Antonina Coppola, Maria Pitrone, Giuseppe Pizzo, Giuseppina Campisi, Giuseppe Pizzolanti, Carla Giordano
Format: Article
Language:English
Published: BMC 2017-08-01
Series:Stem Cell Research & Therapy
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13287-017-0633-z
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author Laura Tomasello
Rodolfo Mauceri
Antonina Coppola
Maria Pitrone
Giuseppe Pizzo
Giuseppina Campisi
Giuseppe Pizzolanti
Carla Giordano
author_facet Laura Tomasello
Rodolfo Mauceri
Antonina Coppola
Maria Pitrone
Giuseppe Pizzo
Giuseppina Campisi
Giuseppe Pizzolanti
Carla Giordano
author_sort Laura Tomasello
collection DOAJ
description Abstract Background Chronic periodontal disease is an infectious disease consisting of prolonged inflammation of the supporting tooth tissue and resulting in bone loss. Guided bone regeneration procedures have become common and safe treatments in dentistry, and in this context dental stem cells would represent the ideal solution as autologous cells. In this study, we verified the ability of dental pulp mesenchymal stem cells (DPSCs) and gingival mesenchymal stem cells (GMSCs) harvested from periodontally affected teeth to produce new mineralized bone tissue in vitro, and compared this to cells from healthy teeth. Methods To characterize DPSCs and GMSCs, we assessed colony-forming assay, immunophenotyping, mesenchymal/stem cell phenotyping, stem gene profiling by means of flow cytometry, and quantitative polymerase chain reaction (qPCR). The effects of proinflammatory cytokines on mesenchymal stem cell (MSC) proliferation and differentiation potential were investigated. We also observed participation of several heat shock proteins (HSPs) and actin-depolymerizing factors (ADFs) during osteogenic differentiation. Results DPSCs and GMSCs were successfully isolated both from periodontally affected dental tissue and controls. Periodontally affected dental MSCs proliferated faster, and the inflamed environment did not affect MSC marker expressions. The calcium deposition was higher in periodontally affected MSCs than in the control group. Proinflammatory cytokines activate a cytoskeleton remodeling, interacting with HSPs including HSP90 and HSPA9, thioredoxin-1, and ADFs such as as profilin-1, cofilin-1, and vinculin that probably mediate the increased acquisition in the inflamed environment. Conclusions Our findings provide evidence that periodontally affected dental tissue (both pulp and gingiva) can be used as a source of MSCs with intact stem cell properties. Moreover, we demonstrated that the osteogenic capability of DPSCs and GMSCs in the test group was not only preserved but increased by the overexpression of several proinflammatory cytokine-dependent chaperones and stress response proteins.
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spelling doaj.art-d21881eb964a4ff985c02f5e9736f3122022-12-22T00:08:37ZengBMCStem Cell Research & Therapy1757-65122017-08-018111510.1186/s13287-017-0633-zMesenchymal stem cells derived from inflamed dental pulpal and gingival tissue: a potential application for bone formationLaura Tomasello0Rodolfo Mauceri1Antonina Coppola2Maria Pitrone3Giuseppe Pizzo4Giuseppina Campisi5Giuseppe Pizzolanti6Carla Giordano7Laboratory of Regenerative Medicine “Aldo Galluzzo”, Department of Endocrinology, Diabetology and Metabolism, University of PalermoDepartment of Surgical, Oncological and Oral Sciences, University of PalermoLaboratory of Regenerative Medicine “Aldo Galluzzo”, Department of Endocrinology, Diabetology and Metabolism, University of PalermoLaboratory of Regenerative Medicine “Aldo Galluzzo”, Department of Endocrinology, Diabetology and Metabolism, University of PalermoDepartment of Surgical, Oncological and Oral Sciences, University of PalermoDepartment of Surgical, Oncological and Oral Sciences, University of PalermoLaboratory of Regenerative Medicine “Aldo Galluzzo”, Department of Endocrinology, Diabetology and Metabolism, University of PalermoLaboratory of Regenerative Medicine “Aldo Galluzzo”, Department of Endocrinology, Diabetology and Metabolism, University of PalermoAbstract Background Chronic periodontal disease is an infectious disease consisting of prolonged inflammation of the supporting tooth tissue and resulting in bone loss. Guided bone regeneration procedures have become common and safe treatments in dentistry, and in this context dental stem cells would represent the ideal solution as autologous cells. In this study, we verified the ability of dental pulp mesenchymal stem cells (DPSCs) and gingival mesenchymal stem cells (GMSCs) harvested from periodontally affected teeth to produce new mineralized bone tissue in vitro, and compared this to cells from healthy teeth. Methods To characterize DPSCs and GMSCs, we assessed colony-forming assay, immunophenotyping, mesenchymal/stem cell phenotyping, stem gene profiling by means of flow cytometry, and quantitative polymerase chain reaction (qPCR). The effects of proinflammatory cytokines on mesenchymal stem cell (MSC) proliferation and differentiation potential were investigated. We also observed participation of several heat shock proteins (HSPs) and actin-depolymerizing factors (ADFs) during osteogenic differentiation. Results DPSCs and GMSCs were successfully isolated both from periodontally affected dental tissue and controls. Periodontally affected dental MSCs proliferated faster, and the inflamed environment did not affect MSC marker expressions. The calcium deposition was higher in periodontally affected MSCs than in the control group. Proinflammatory cytokines activate a cytoskeleton remodeling, interacting with HSPs including HSP90 and HSPA9, thioredoxin-1, and ADFs such as as profilin-1, cofilin-1, and vinculin that probably mediate the increased acquisition in the inflamed environment. Conclusions Our findings provide evidence that periodontally affected dental tissue (both pulp and gingiva) can be used as a source of MSCs with intact stem cell properties. Moreover, we demonstrated that the osteogenic capability of DPSCs and GMSCs in the test group was not only preserved but increased by the overexpression of several proinflammatory cytokine-dependent chaperones and stress response proteins.http://link.springer.com/article/10.1186/s13287-017-0633-zInflammationDental diseasePulpal and gingival mesenchymal stem cellsBone formationHeat shock proteinADFs
spellingShingle Laura Tomasello
Rodolfo Mauceri
Antonina Coppola
Maria Pitrone
Giuseppe Pizzo
Giuseppina Campisi
Giuseppe Pizzolanti
Carla Giordano
Mesenchymal stem cells derived from inflamed dental pulpal and gingival tissue: a potential application for bone formation
Stem Cell Research & Therapy
Inflammation
Dental disease
Pulpal and gingival mesenchymal stem cells
Bone formation
Heat shock protein
ADFs
title Mesenchymal stem cells derived from inflamed dental pulpal and gingival tissue: a potential application for bone formation
title_full Mesenchymal stem cells derived from inflamed dental pulpal and gingival tissue: a potential application for bone formation
title_fullStr Mesenchymal stem cells derived from inflamed dental pulpal and gingival tissue: a potential application for bone formation
title_full_unstemmed Mesenchymal stem cells derived from inflamed dental pulpal and gingival tissue: a potential application for bone formation
title_short Mesenchymal stem cells derived from inflamed dental pulpal and gingival tissue: a potential application for bone formation
title_sort mesenchymal stem cells derived from inflamed dental pulpal and gingival tissue a potential application for bone formation
topic Inflammation
Dental disease
Pulpal and gingival mesenchymal stem cells
Bone formation
Heat shock protein
ADFs
url http://link.springer.com/article/10.1186/s13287-017-0633-z
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