ADAMTS12 Depletion by Insulin in OUMS-27 Human Chondrosarcoma Cells
Aynur ALTUNTAŞ1, Sümeyya AKYOL2, Bahattin ADAM3, Özlem ÇAKMAK4, Veli UĞURCU5, Gönül ERDEN6, Yunus YÜKSELTEN7, Kadir DEMİRCAN2
1Department of Chemistry, Ankara Regional Office of Council of Forensic Medicine, Ankara, Turkey
2Department of Medical Biology, Medical Faculty of Turgut Özal University, Ankara, Turkey
3Department of Medical Biochemistry, Mevlana University Medical School, Konya, Turkey; San Jose State University, San Jose, California, USA
4Department of Biology Education, Gazi University, Faculty of Education, Ankara, Turkey
5Department of Medical Biochemistry, Dumlupinar University Medical Faculty, Kutahya, Turkey
6Department of Medical Biochemistry, Hacettepe University Medical School, Ankara, Turkey
7Department of Medical Biology, Medical Faculty of Ankara University, Ankara, Turkey
Keywords: ADAMTS12, cartilage tissue, insulin, OUMS-27
Objectives: In this study, we aim to investigate the association between articular damage in diabetes and a disintegrin-like and metalloproteinase with thrombospondin motifs 12 (ADAMTS12) at gene expression and protein levels.
Materials and methods: OUMS-27 human chondrosarcoma cells were used to investigate how ADAMTS12 levels changed in vitro condition in presence and absence of insulin. The study included three groups of cells treated with 10 μg/mL of insulin, and a control group. Cells were incubated with insulin in medium for one day, three days, and seven days. The effects of insulin on ADAMTS12 were investigated at both gene expression and protein levels. The relationships between the variables were tested by Mann-Whitney U test.
Results: ADAMTS12 expression was significantly lower in the groups treated with insulin medium for one day and seven day periods (p=0.008 and p=0.008, respectively) compared to the control group. No significant difference was detected in the expression level between the groups kept in insulin medium for three days and the control group (p=0.55). In addition, protein amounts of the groups exposed to insulin medium for one, three, and seven day periods were lower.
Conclusion: Insulin reduces the amount of ADAMTS12 which causes delayed recovery of cartilage tissue in the OUMS-27 cell lines utilized in our study for their chondrocytic properties. This reduction due to insulin treatment may contribute to recovery of cartilage tissue.
The authors declared no conflicts of interest with respect to the authorship and/or publication of this article.
The authors received no financial support for the research and/or authorship of this article.