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Isolation, Characterization, and Differentiation of Dental Pulp Stem Cells in Ferrets.
Homayounfar, Negar; Verma, Prashant; Nosrat, Ali; El Ayachi, Ikbale; Yu, Zongdong; Romberg, Elaine; Huang, George T-J; Fouad, Ashraf F.
Afiliação
  • Homayounfar N; Department of Endodontics, Periodontics and Prosthodontics, School of Dentistry, University of Maryland, Baltimore, Maryland.
  • Verma P; Department of Endodontics, Periodontics and Prosthodontics, School of Dentistry, University of Maryland, Baltimore, Maryland.
  • Nosrat A; Department of Endodontics, Periodontics and Prosthodontics, School of Dentistry, University of Maryland, Baltimore, Maryland.
  • El Ayachi I; Department of Bioscience Research, College of Dentistry, University of Tennessee Health Science Center, Memphis, Tennessee.
  • Yu Z; Department of Bioscience Research, College of Dentistry, University of Tennessee Health Science Center, Memphis, Tennessee.
  • Romberg E; Department of Endodontics, Periodontics and Prosthodontics, School of Dentistry, University of Maryland, Baltimore, Maryland.
  • Huang GT; Department of Bioscience Research, College of Dentistry, University of Tennessee Health Science Center, Memphis, Tennessee.
  • Fouad AF; Department of Endodontics, University of North Carolina, Chapel Hill, North Carolina. Electronic address: afouad@unc.edu.
J Endod ; 42(3): 418-24, 2016 Mar.
Article em En | MEDLINE | ID: mdl-26794343
ABSTRACT

INTRODUCTION:

The ferret canine tooth has been introduced as a suitable model for studying dental pulp regeneration. The aim of this study was to isolate and characterize ferret dental pulp stem cells (fDPSCs) and their differentiation potential.

METHODS:

Dental pulp stem cells were isolated from freshly extracted ferret canine teeth. The cells were examined for the expression of stem cell markers STRO-1, CD90, CD105, and CD146. The osteo/odontogenic and adipogenic differentiation potential of fDPSCs was evaluated. Osteogenic and odontogenic marker genes were evaluated using quantitative real-time polymerase chain reaction (qRT-PCR) on days 1, 4, and 8 after osteo/odontogenic induction of fDPSCs including dentin sialophosphoprotein (DSPP), dentin matrix protein-1, osteopontin, and alkaline phosphatase. Human dental pulp cells were used as the control. The results were analyzed using 3-way analysis of variance.

RESULTS:

fDPSCs were positive for STRO1, CD90, and CD105 and negative for CD146 markers with immunohistochemistry. fDPSCs showed strong osteogenic and weak adipogenic potential. The overall expression of DSPP was not significantly different between fDPSCs and human dental pulp cells. The expression of DSPP in osteo/odontogenic media was significantly higher in fDPSCs on day 4 (P < .01). The overall expression of dentin matrix protein-1, osteopontin, and alkaline phosphatase was significantly higher in fDPSCs (P = .0005).

CONCLUSIONS:

fDPSCs were positive for several markers of dental pulp stem cells resembling human DPSCs and appeared to show a stronger potential to differentiate to osteoblastic rather than odontoblastic lineage.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células-Tronco / Polpa Dentária / Furões Limite: Animals / Female / Humans / Male Idioma: En Revista: J Endod Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células-Tronco / Polpa Dentária / Furões Limite: Animals / Female / Humans / Male Idioma: En Revista: J Endod Ano de publicação: 2016 Tipo de documento: Article