Oncotarget

Research Papers:

In vitro functional characterization of prostaglandin-endoperoxide synthase 2 during chondrocyte hypertrophic differentiation

Na Li _, Qian Wang, Ting Zhu, Longwei Qiao, Fei Zhang, Rui Mi, Bo Wang, Lin Chen, Junxia Gu, Yaojuan Lu and Qiping Zheng

PDF  |  HTML  |  How to cite

Oncotarget. 2016; 7:36280-36292. https://doi.org/10.18632/oncotarget.8889

Metrics: PDF 1652 views  |   HTML 3848 views  |   ?  


Abstract

Na Li1,*, Qian Wang1,*, Ting Zhu1, Longwei Qiao2, Fei Zhang1, Rui Mi1, Bo Wang1, Lin Chen3, Junxia Gu1, Yaojuan Lu1, Qiping Zheng1

1Department of Hematological Laboratory Science, Jiangsu Key Laboratory of Medical Science and Laboratory Medicine, School of Medicine, Jiangsu University, Zhenjiang 212013, China

2Center for Reproduction and Genetics, Suzhou Hospital Affiliated to Nanjing Medical University, Suzhou, Jiangsu, 215002, China

3State Key Laboratory of Trauma, Burns and Combined Injury, Center of Bone Metabolism and Repair, Trauma Center, Institute of Surgery Research, Daping Hospital, Third Military Medical University, Chongqing, 400042, China

*These authors have contributed equally to this work

Correspondence to:

Qiping Zheng, e-mail: [email protected]

Yaojuan Lu, e-mail: [email protected]

Keywords: Cox-2, Col10a1 expression, chondrocyte hypertrophy, ATDC5, Runx2 and Alp

Received: December 21, 2015    Accepted: April 04, 2016    Published: April 21, 2016

ABSTRACT

Cyclooxygenase 2 (Cox-2) has been implicated an essential role during bone repair, but the mechanisms remain elusive. Bone repair healing is known to include processes similar to endochondral ossification. In this study, we investigated the in vitro effect of Cox-2 on Col10a1 expression and chondrocyte hypertrophy, two critical components of endochondral ossification. Using quantitative RT-PCR, we detected increased mRNA levels of Cox-2 and Col10a1 in hypertrophic MCT cells, while cells treated with Cox-2 inhibitor, NS398, showed decreased mRNA and protein levels of Cox-2 and Col10a1. Increased Cox-2 also correlated with significantly upregulated Col10a1 in hypertrophic ATDC5 cells, whereas inhibition of Cox-2 significantly decreased Col10a1 expression. We further generated a Cox-2-expressing ATDC5 stable cell line. Compared with the controls, Cox-2 over-expression significantly increased Col10a1 as early as day 7 of continuous culturing, but not at days 14 and 21. Enhanced Alp staining was also observed in day 7 stable cell line. Correspondingly, we detected significantly increased levels of Runx2, Alp, Bcl-2, Bax, Col1a1, Osterix, and Bsp in day 7 stable line. Most of these genes have been associated with chondrocyte maturation and apoptosis. Together, our results support that Cox-2 promotes Col10a1 expression and chondrocyte hypertrophy in vitro, possibly through upregulation of Runx2 and other relevant transcription factors.


Creative Commons License All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 4.0 License.
PII: 8889