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Characterization and evaluation of ascorbic acid-induced cell sheet formation in human periodontal ligament stem cells: An in vitro study.
Ashok, Karishma; Thomas, Biju; Manjappa, Akshay Bairapura; Shetty, Jayaprakasha; Rao, Shama; Basavarajappa, Mohana Kumar; Ramesh, Amitha.
Afiliação
  • Ashok K; Department of Periodontics, A. B. Shetty Memorial Institute of Dental Sciences, Nitte (Deemed to be University), Mangaluru, 575018, India.
  • Thomas B; Department of Periodontics, A. B. Shetty Memorial Institute of Dental Sciences, Nitte (Deemed to be University), Mangaluru, 575018, India. Electronic address: bijunicy@yahoo.co.uk.
  • Manjappa AB; Nitte University Centre for Stem Cell Research and Regenerative Medicine, K. S. Hegde Medical Academy, Nitte (Deemed to be University), Mangaluru, 575018, India.
  • Shetty J; Nitte University Centre for Stem Cell Research and Regenerative Medicine, K. S. Hegde Medical Academy, Nitte (Deemed to be University), Mangaluru, 575018, India.
  • Rao S; Nitte University Centre for Stem Cell Research and Regenerative Medicine, K. S. Hegde Medical Academy, Nitte (Deemed to be University), Mangaluru, 575018, India.
  • Basavarajappa MK; Nitte University Centre for Stem Cell Research and Regenerative Medicine, K. S. Hegde Medical Academy, Nitte (Deemed to be University), Mangaluru, 575018, India.
  • Ramesh A; Department of Periodontics, A. B. Shetty Memorial Institute of Dental Sciences, Nitte (Deemed to be University), Mangaluru, 575018, India.
J Oral Biosci ; 63(4): 429-435, 2021 12.
Article em En | MEDLINE | ID: mdl-34666146
ABSTRACT

OBJECTIVES:

Periodontal ligament-derived stem cells (PDLSCs) are regarded as a viable option for periodontal regeneration using cell sheet technology. The objective of the present in vitro study was to characterize human PDLSCs based on their phenotypic and biological properties and to evaluate the ascorbic acid (AA or vitamin C)-induced cell sheet by analyzing the molecular markers.

METHODS:

PDLSCs were established from premolars, and their morphology, viability, proliferation, phenotypic marker expression, and ability to differentiate into osteocytes and adipocytes were analyzed. PDLSCs were then induced to form cell sheets using 100 µM AA, and gene expression was examined by real-time polymerase chain reaction.

RESULTS:

PDLSCs showed fibroblastic morphology with >95% viability. The cells were highly proliferative and positive for surface antigens CD29, CD73, and CD90 but negative for CD34 and CD45. They were capable of differentiating into osteocytes and adipocytes. Induction with 100 µM AA transformed PDLSCs into two-to three-layered cell sheets. There was no significant upregulation in ALP and RUNX2 expression in the AA-induced cell sheet. However, the expression levels of late osteoblast differentiation marker (bone gamma-carboxy glutamate protein); cementogenic markers (cementum attachment protein and CP23), and genes encoding extracellular matrix (ECM) proteins [collagen type 1 alpha 1 and integrin beta 1) were higher in AA-induced cell sheets by PDLSCs.

CONCLUSIONS:

The stimulating effect of AA on cell sheet formation by PDLSCs was confirmed by the expression of typical markers involved in osteogenesis/cementogenesis and ECM secretion, which makes this procedure a prospective option for periodontal tissue regeneration applications.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ligamento Periodontal / Células-Tronco Tipo de estudo: Observational_studies Limite: Humans Idioma: En Revista: J Oral Biosci Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Índia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ligamento Periodontal / Células-Tronco Tipo de estudo: Observational_studies Limite: Humans Idioma: En Revista: J Oral Biosci Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Índia