Author(s):
Silva, M. L. Alves da ; Pinto, A. R. ; Martins, A. ; Correlo, V. M. ; Sol, P. C. ; Bhattacharya, Mrinal ; Faria, Susana ; Reis, R. L. ; Neves, N. M.
Date: 2015
Persistent ID: http://hdl.handle.net/1822/27057
Origin: RepositóriUM - Universidade do Minho
Project/scholarship:
info:eu-repo/grantAgreement/EC/FP7/316331/EU;
info:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F28708%2F2006/PT;
Subject(s): Cartilage; Chondrogenic differentiation; Conditioned medium; Stem cells; Science & Technology
Description
Paracrine signalling from chondrocytes has been reported to increase the synthesis and expression of cartilage extracellular matrix (ECM) by stem cells. The use of conditioned medium obtained from chondrocytes for stimulating stem cells chondrogenic differentiation may be a very interesting alternative for moving into the clinical application of these cells, as chondrocytes could be partially replaced by stem cells for this type of application. In the present study we aimed to achieve chondrogenic differentiation of two different sources of stem cells using conditioned medium, without adding growth factors. We tested both human bone marrow-derived mesenchymal stem cells (hBSMCs) and human Wharton’s jelly-derived stem cells (hWJSCs). Conditioned medium obtained from a culture of human articular chondrocytes was used to feed the cells during the experiment. Cultures were performed in previously produced three-dimensional (3D) scaffolds, composed of a blend of 50:50 chitosan:poly(butylene succinate). Both types of stem cells were able to undergo chondrogenic differentiation without the addition of growth factors. Cultures using hWJSCs showed significantly higher GAGs accumulation and expression of cartilage-related genes (aggrecan, Sox9 and collagen type II) when compared to hBMSCs cultures. Conditioned medium obtained from articular chondrocytes induced the chondrogenic differentiation of MSCs and ECM formation. Obtained results showed that this new strategy is very interesting and should be further explored for clinical applications.
M. Alves da Silva would like to acknowledge the Portuguese Foundation for Science and Technology (FCT; Grant No. SFRH/BD/28708/2006). The authors would like to acknowledge the patients of Hospital de S. Marcos, Braga, Portugal, for donation of biological samples, as well as the medical and nursing staff. The authors would also like to thank the Institute for Health and Life Sciences (ICVS), University of Minho, Braga, Portugal, for allowing the use of their research facilities; to Luis Martins for his valuable help with the histological procedures; and Goreti Pinto for aid with microscopy. The research leading to these results has received funding from the European Union's Seventh Framework Programme (FP7/2007-2013; Grant No. REGPOT-CT2012-316331-POLARIS).
