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Human periodontal ligament stem cells with distinct osteogenic potential induce bone formation in rat calvaria defects

This study aimed to evaluate the ability of human periodontal ligament stem cells (PDLSCs) with high (HP-PDLSCs) and low (LP-PDLSCs) osteogenic potential, in addition to mixed cells, to repair bone tissue. Cell phenotype, proliferation and differentiation were evaluated. Undifferentiated PDLSCs were...

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Published in:Regenerative medicine 2022-06, Vol.17 (6), p.341-353
Main Authors: Adolpho, Leticia Faustino, Lopes, Helena Bacha, Freitas, Gileade Pereira, Weffort, Denise, Campos Totoli, Gabriela Guaraldo, Loyola Barbosa, Ana Carolina, Freire Assis, Rahyza Inacio, Silverio Ruiz, Karina Gonzales, Andia, Denise Carleto, Rosa, Adalberto Luiz, Beloti, Marcio Mateus
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creator Adolpho, Leticia Faustino
Lopes, Helena Bacha
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Rosa, Adalberto Luiz
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description This study aimed to evaluate the ability of human periodontal ligament stem cells (PDLSCs) with high (HP-PDLSCs) and low (LP-PDLSCs) osteogenic potential, in addition to mixed cells, to repair bone tissue. Cell phenotype, proliferation and differentiation were evaluated. Undifferentiated PDLSCs were injected into rat calvarial defects and the new bone was evaluated by μCT, histology and real-time PCR. PDLSCs exhibited a typical mesenchymal stem cell phenotype and HP-PDLSCs showed lower proliferative and higher osteogenic potential than LP-PDLSCs. PDLSCs induced similar bone formation and histological analysis suggests a remodeling process, confirmed by osteogenic and osteoclastogenic markers, especially in tissues derived from defects treated with HP-PDLSCs. PDLSCs induced similar bone formation irrespective of their osteogenic potential. Bone is one of the most transplanted tissues worldwide and cell-based therapies has been investigated as an alternative for the treatment of bone defects. Dental tissues have been investigated as sources of stem cells and the periodontal ligament has been shown to be a viable source of these cells. Stem cells from periodontal ligament induce significant bone formation in rat calvaria defects and are safe for cell-based therapies, as the cells remain at the bone defect site for up to 4 weeks and do not migrate to vital organs, such as brain, heart, lungs, spleen, kidneys, and liver in the same period. In addition, immune responses were not detected. Considering that, stem cells from periodontal ligament can be useful in cell therapy strategies to induce bone regeneration.
doi_str_mv 10.2217/rme-2021-0178
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Cell phenotype, proliferation and differentiation were evaluated. Undifferentiated PDLSCs were injected into rat calvarial defects and the new bone was evaluated by μCT, histology and real-time PCR. PDLSCs exhibited a typical mesenchymal stem cell phenotype and HP-PDLSCs showed lower proliferative and higher osteogenic potential than LP-PDLSCs. PDLSCs induced similar bone formation and histological analysis suggests a remodeling process, confirmed by osteogenic and osteoclastogenic markers, especially in tissues derived from defects treated with HP-PDLSCs. PDLSCs induced similar bone formation irrespective of their osteogenic potential. Bone is one of the most transplanted tissues worldwide and cell-based therapies has been investigated as an alternative for the treatment of bone defects. Dental tissues have been investigated as sources of stem cells and the periodontal ligament has been shown to be a viable source of these cells. Stem cells from periodontal ligament induce significant bone formation in rat calvaria defects and are safe for cell-based therapies, as the cells remain at the bone defect site for up to 4 weeks and do not migrate to vital organs, such as brain, heart, lungs, spleen, kidneys, and liver in the same period. In addition, immune responses were not detected. 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subjects Animals
bone
Cell Differentiation
Cell Proliferation
cell therapy
Cells, Cultured
Humans
osteoblast
Osteogenesis
Periodontal Ligament
Rats
Skull
stem cell
Stem Cells
title Human periodontal ligament stem cells with distinct osteogenic potential induce bone formation in rat calvaria defects
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