Affiliations 

  • 1 Faculty of Engineering and Informatics, School of Engineering, Medical and Healthcare Technology Department, University of Bradford, Bradford BD7 1DP, UK; Tissue Engineering Group, Chemical Biology and Biomedical Engineering, Stevens Institute of Technology, Hoboken, NJ 07030, USA
  • 2 Faculty of Engineering and Informatics, School of Engineering, Medical and Healthcare Technology Department, University of Bradford, Bradford BD7 1DP, UK. Electronic address: m.youseffi@bradford.ac.uk
  • 3 Faculty of Engineering and Informatics, School of Engineering, Medical and Healthcare Technology Department, University of Bradford, Bradford BD7 1DP, UK
  • 4 Biosensor and Bioengineering Laboratory, MiNT-SRC Research Centre, Universiti Tun Hussein Onn Malaysia, 86400 Parit Raja, Batu Pahat, Johor, Malaysia
  • 5 Department of Pharmacy, School of Applied Sciences, University of Huddersfield, Huddersfield HD1 3DH, UK
Cytokine, 2016 07;83:118-126.
PMID: 27108397 DOI: 10.1016/j.cyto.2016.04.008

Abstract

Articular cartilage is an avascular and flexible connective tissue found in joints. It produces a cushioning effect at the joints and provides low friction to protect the ends of the bones from wear and tear/damage. It has poor repair capacity and any injury can result pain and loss of mobility. Transforming growth factor-beta (TGF-β), a cytokine superfamily, regulates cell function, including differentiation and proliferation. Although the function of the TGF-βs in various cell types has been investigated, their function in cartilage repair is as yet not fully understood. The effect of TGF-β3 in biological regulation of primary chondrocyte was investigated in this work. TGF-β3 provided fibroblastic morphology to chondrocytes and therefore overall reduction in cell proliferation was observed. The length of the cells supplemented with TGF-β3 were larger than the cells without TGF-β3 treatment. This was caused by the fibroblast like cells (dedifferentiated chondrocytes) which occupied larger areas compared to cells without TGF-β3 addition. The healing process of the model wound closure assay of chondrocyte multilayer was slowed down by TGF-β3, and this cytokine negatively affected the strength of chondrocyte adhesion to the cell culture surface.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.