P111 Tenocytes extracted from rotator cuff tendons induce TNAP-dependent mineral deposition and express genes related to a hypertrophic chondrocyte differentiation

التفاصيل البيبلوغرافية
العنوان: P111 Tenocytes extracted from rotator cuff tendons induce TNAP-dependent mineral deposition and express genes related to a hypertrophic chondrocyte differentiation
المؤلفون: Frédéric Blanchard, B. Le Goff, Aurélie Najm, Paul Arnolfo, T Garraud, Christelle Darrieutort-Laffite
المصدر: Abstracts.
بيانات النشر: BMJ Publishing Group Ltd and European League Against Rheumatism, 2019.
سنة النشر: 2019
مصطلحات موضوعية: business.industry, Scleraxis, Phosphodiesterase, chemistry.chemical_element, Calcium, Phenotype, Tendon, Tenomodulin, Staining, Andrology, medicine.anatomical_structure, chemistry, medicine, Rotator cuff, business
الوصف: Career situation of first and presenting author Resident. Introduction Calcific tendinopathy represents 10% to 42% of chronic painful shoulders. These calcium deposits are composed of carbonated apatite. Although the disease is frequent, its origin stays still largely unknown. Our previous results showed that calcific deposits are surrounded by chondrocyte-like cells expressing TNAP (Tissue Nonspecific Alkaline Phosphatase) and ENPP1 (Ectonucleotidepyrophosphatase/phosphodiesterase 1), two key enzymes involved in the mineralization process. Objectives To study the ability of cells extracted from rotator cuff tendons to produce apatite crystals and to analyze the phenotype of these mineralizing cells. Methods Tenocytes were extracted from rotator cuff tendons removed during shoulder total replacement. To evaluate their ability to mineralize, they were cultured in an osteogenic medium (OM) for 21 days. Mineral deposition then was assessed by staining with Alizarin red. Tenocytes total RNA was extracted and analyzed by RT-qPCRs. TNAP enzymatic activity was also assessed in the cells. A TNAP inhibitor was used to delineate its implication in the mineralization process. Results Tendon samples were obtained from 5 patients (age 69.6±5.13 years). Cells extracted from these tendons expressed collagen I, collagen III, Scleraxis and Mkx (Mohawk homeobox), as expected for tenocytes. However, Tenomodulin was very weakly expressed and lost after passage 1. These cells were able to mineralize in the OM although no mineralization was observed in the control medium. qPCR analyses showed a significant increase of TNAP and ENPP1 expression by cells cultured in OM (p Conclusions Tenocyte-like cells extracted from tendons of the rotator cuff are able to induce mineralization in an osteogenic medium. The cells express genes associated with a hypertrophic chondrocyte phenotype (TNAP, COL10 and MMP13) and TNAP seems to have a crucial role in the induced mineralization. These results suggest that tenocytes could differentiate into hypertrophic chondrocyte which induce TNAP-dependent apatite deposition in calcific tendonitis. Acknowledgements This study was supported by Inserm and the French Society of Rheumatology. Disclosure of Interest None declared.
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::51240f83d4c3bae4a1881771adfcb93dTest
https://doi.org/10.1136/annrheumdis-2018-ewrr2019.99Test
رقم الانضمام: edsair.doi...........51240f83d4c3bae4a1881771adfcb93d
قاعدة البيانات: OpenAIRE