Osteogenic potential of mesenchymal cells derived from canine umbilical cord matrix co-cultured with platelet-rich plasma and demineralized bone matrix.
10.4142/jvs.2015.16.3.381
- Author:
Talita F B SOUZA
1
;
Silmara S SAKAMOTO
;
Gabriel T N M FERREIRA
;
Roberto GAMEIRO
;
Marcia MARINHO
;
Alexandre L DE ANDRADE
;
Tereza C CARDOSO
Author Information
1. Laboratory of Animal Virology and Cell Culture, College of Veterinary Medicine, UNESP-Universidade Estadual Paulista, Aracatuba, SP 16050-680, Brazil. tcardoso@fmva.unesp.br
- Publication Type:Brief Communication ; Research Support, Non-U.S. Gov't
- Keywords:
bone;
mesenchymal stem cells;
platelet-rich plasma;
umbilical cord
- MeSH:
Animals;
Bone Demineralization Technique/veterinary;
Bone Matrix/*metabolism;
Cell Differentiation;
Cells, Cultured;
Coculture Techniques/veterinary;
Dogs;
Mesenchymal Stromal Cells/*metabolism;
*Osteogenesis;
Platelet-Rich Plasma/*metabolism;
Umbilical Cord/metabolism
- From:Journal of Veterinary Science
2015;16(3):381-384
- CountryRepublic of Korea
- Language:English
-
Abstract:
Canine mesenchymal cells (MSCs) derived from Wharton's jelly were co-cultured, then supplemented or not supplemented with platelet rich plasma (PRP) and demineralized bone matrix (DBM) to verify osteogenic differentiation. Osteoblastic differentiation followed by mineralized bone matrix production was found to be significantly higher (p < 0.05) when MSCs were associated with PRP/DBM in culture after 14-21-days of induction. Osteopontin and osteocalcin gene expression were significantly superior (p < 0.05) under the same culture conditions after 21 days of observation. In conclusion, addition of PRP to DBM co-cultured with MSCs successfully induced osteogenesis in vitro.