Effects of serum-free culture media on human apical papilla cells properties.


Journal

Archives of oral biology
ISSN: 1879-1506
Titre abrégé: Arch Oral Biol
Pays: England
ID NLM: 0116711

Informations de publication

Date de publication:
Jan 2021
Historique:
received: 23 07 2020
revised: 11 09 2020
accepted: 19 10 2020
pubmed: 11 11 2020
medline: 3 2 2021
entrez: 10 11 2020
Statut: ppublish

Résumé

Aiming at more effective and safer cell therapies, the objective of this study was to evaluate the biological properties of human apical papilla cells cultured in the absence of serum supplementation in comparison to cells cultured with fetal bovine serum (FBS). Two apical papilla cell populations were isolated from third molars with incomplete rhizogenesis, and cultured in four different media: minimum essential Eagle medium - alpha modification (alpha-MEM); alpha-MEM supplemented with FBS (alpha-MEM + FBS); Dulbecco's modified Eagle medium/nutrient mixture F-12 (DMEM/F12); and DMEM/F12 supplemented with FBS (DMEM/F12 + FBS). We evaluated their proliferation, clonogenicity, and in vitro osteogenic and chondrogenic differentiation potential. Apical papilla cells cultured in DMEM/F12 + FBS and alpha-MEM + FBS were more proliferative than those grown in serum-free media, and also exhibited greater efficiency in colony cell formation. Despite this, all study groups showed immunostaining for the marker of mitosis anti-PHH3. Also, alpha-MEM + FBS, alpha-MEM, and DMEM/F12 + FBS exhibited higher amount of mineralized deposits in vitro than DMEM/F12, while only cells cultured with FBS were able to form spheres in chondrogenic differentiation assay. Our results showed that, although the cultivation of apical papilla cells in a serum-free medium has reduced the properties of cell proliferation and differentiation, these cells are still capable of maintaining their desirable characteristics.

Identifiants

pubmed: 33171394
pii: S0003-9969(20)30340-X
doi: 10.1016/j.archoralbio.2020.104962
pii:
doi:

Substances chimiques

Culture Media, Serum-Free 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104962

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Auteurs

Aline Queiroz (A)

Laboratory of Stem Cell Biology in Dentistry - LABITRON, Oral and Maxillofacial Pathology Department, School of Dentistry, University of São Paulo, Av Professor Lineu Prestes, 2227, 05508-000, São Paulo, SP, Brazil. Electronic address: aline.queiroz@usp.br.

Mariana Taira Wada (MT)

Laboratory of Stem Cell Biology in Dentistry - LABITRON, Oral and Maxillofacial Pathology Department, School of Dentistry, University of São Paulo, Av Professor Lineu Prestes, 2227, 05508-000, São Paulo, SP, Brazil. Electronic address: mariana.wada@usp.br.

Flávia Cristina Perillo Rosin (FCP)

General Pathology Department, School of Dentistry, University of São Paulo, Av Professor Lineu Prestes, 2227, 05508-000, São Paulo, SP, Brazil. Electronic address: flarosin@usp.br.

Cibele Pelissari (C)

Laboratory of Stem Cell Biology in Dentistry - LABITRON, Oral and Maxillofacial Pathology Department, School of Dentistry, University of São Paulo, Av Professor Lineu Prestes, 2227, 05508-000, São Paulo, SP, Brazil. Electronic address: cibele.santos@usp.br.

Marília Trierveiler (M)

Laboratory of Stem Cell Biology in Dentistry - LABITRON, Oral and Maxillofacial Pathology Department, School of Dentistry, University of São Paulo, Av Professor Lineu Prestes, 2227, 05508-000, São Paulo, SP, Brazil. Electronic address: trierveiler@usp.br.

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Classifications MeSH