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Article

Enumeration and Localization of Mesenchymal Progenitor Cells and Macrophages in Synovium from Normal Individuals and Patients with Pre-Osteoarthritis or Clinically Diagnosed Osteoarthritis

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McCaig Institute for Bone & Joint Health, University of Calgary, Calgary, AB T2N4N1, Canada
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Department Cell Biology and Anatomy, University of Calgary, Calgary, AB T2N4N1, Canada
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Department of Pathology & Laboratory Medicine, University of Calgary, Calgary, AB T2N4N1, Canada
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Department of Surgery, University of Calgary, Calgary, AB T2N4N1, Canada
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Department of Comparative Biology and Experimental Medicine, University of Calgary, Calgary, AB T2N4N1, Canada
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The D-BOARD European Consortium for Biomarker Discovery, School of Veterinary Medicine, Faculty of Health and Medical Sciences, University of Surrey, Guildford GU2 7XH, UK
*
Author to whom correspondence should be addressed.
Academic Editors: Ali Mobasheri and Charles J. Malemud
Int. J. Mol. Sci. 2017, 18(4), 774; https://doi.org/10.3390/ijms18040774
Received: 31 January 2017 / Revised: 11 March 2017 / Accepted: 28 March 2017 / Published: 5 April 2017
(This article belongs to the Section Biochemistry)
Osteoarthritis (OA) is a degenerative disorder characterized by chondrocyte apoptosis and degeneration of articular cartilage resulting in loss of mobility and pain. Inflammation plays a key role in the development and progression of OA both on the side of apoptosis and repair, while its exact role in pathogenesis has yet to be fully elucidated. Few studies have examined the cellular composition (inflammatory cells and/or progenitor cells) in the synovium of patients with pre-OA (asymptomatic with cartilage damage). Therefore, in the current study, mesenchymal progenitor cells (MPCs) and macrophages were enumerated within normal, pre-OA and OA synovium. No differences were observed between MPCs in normal vs. pre-OA, however, fewer macrophages were observed in pre-OA vs. normal synovium. Osteoarthritic synovium contained greater numbers of both MPCs and macrophages. Interestingly, the localization of MPCs and macrophages was affected by disease severity. In normal and pre-OA synovium, MPCs and macrophages co-localized, while in OA synovium, MPCs and macrophage populations were spatially distinct. Examining the cellular interactions between MPCs and macrophages in synovium may be essential for understanding the role of these cells in the onset and/or pathogenesis of the disease. This study has provided a first step by examining these cell types both spatially and temporally (e.g., disease severity). Further cellular and molecular studies will be needed to determine the functions of these cells in the context of disease and in relation to each other and the joint as a whole. View Full-Text
Keywords: adult progenitor cells; osteoarthritis; macrophage; synovium adult progenitor cells; osteoarthritis; macrophage; synovium
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MDPI and ACS Style

O’Brien, K.; Tailor, P.; Leonard, C.; DiFrancesco, L.M.; Hart, D.A.; Matyas, J.R.; Frank, C.B.; Krawetz, R.J. Enumeration and Localization of Mesenchymal Progenitor Cells and Macrophages in Synovium from Normal Individuals and Patients with Pre-Osteoarthritis or Clinically Diagnosed Osteoarthritis. Int. J. Mol. Sci. 2017, 18, 774. https://doi.org/10.3390/ijms18040774

AMA Style

O’Brien K, Tailor P, Leonard C, DiFrancesco LM, Hart DA, Matyas JR, Frank CB, Krawetz RJ. Enumeration and Localization of Mesenchymal Progenitor Cells and Macrophages in Synovium from Normal Individuals and Patients with Pre-Osteoarthritis or Clinically Diagnosed Osteoarthritis. International Journal of Molecular Sciences. 2017; 18(4):774. https://doi.org/10.3390/ijms18040774

Chicago/Turabian Style

O’Brien, Kate, Pankaj Tailor, Catherine Leonard, Lisa M. DiFrancesco, David A. Hart, John R. Matyas, Cyril B. Frank, and Roman J. Krawetz. 2017. "Enumeration and Localization of Mesenchymal Progenitor Cells and Macrophages in Synovium from Normal Individuals and Patients with Pre-Osteoarthritis or Clinically Diagnosed Osteoarthritis" International Journal of Molecular Sciences 18, no. 4: 774. https://doi.org/10.3390/ijms18040774

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