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      Single Cell Confocal Raman Spectroscopy of Human Osteoarthritic Chondrocytes: A Preliminary Study

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          Abstract

          A great deal of effort has been focused on exploring the underlying molecular mechanism of osteoarthritis (OA) especially at the cellular level. We report a confocal Raman spectroscopic investigation on human osteoarthritic chondrocytes. The objective of this investigation is to identify molecular features and the stage of OA based on the spectral signatures corresponding to bio-molecular changes at the cellular level in chondrocytes. In this study, we isolated chondrocytes from human osteoarthritic cartilage and acquired Raman spectra from single cells. Major spectral differences between the cells obtained from different International Cartilage Repair Society (ICRS) grades of osteoarthritic cartilage were identified. During progression of OA, a decrease in protein content and an increase in cell death were observed from the vibrational spectra. Principal component analysis and subsequent cross-validation was able to associate osteoarthritic chondrocytes to ICRS Grade I, II and III with specificity 100.0%, 98.1%, and 90.7% respectively, while, sensitivity was 98.6%, 82.8%, and 97.5% respectively. The overall predictive efficiency was 92.2%. Our pilot study encourages further use of Raman spectroscopy as a noninvasive and label free technique for revealing molecular features associated with osteoarthritic chondrocytes.

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          Most cited references47

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          Osteoarthritis cartilage histopathology: grading and staging.

          Current osteoarthritis (OA) histopathology assessment methods have difficulties in their utility for early disease, as well as their reproducibility and validity. Our objective was to devise a more useful method to assess OA histopathology that would have wide application for clinical and experimental OA assessment and would become recognized as the standard method. An OARSI Working Group deliberated on principles, standards and features for an OA cartilage pathology assessment system. Using current knowledge of the pathophysiology of OA morphologic features, a proposed system was presented at OARSI 2000. Subsequently, this was widely circulated for comments amongst experts in OA pathology. An OA cartilage pathology assessment system based on six grades, which reflect depth of the lesion and four stages reflecting extent of OA over the joint surface was developed. The OARSI cartilage OA histopathology grading system appears consistent and simple to apply. Further studies are required to confirm the system's utility.
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            Metabolic syndrome meets osteoarthritis.

            Metabolic osteoarthritis (OA) has now been characterized as a subtype of OA, and links have been discovered between this phenotype and metabolic syndrome (MetS)--both with individual MetS components and with MetS as a whole. Hypertension associates with OA through subchondral ischaemia, which can compromise nutrient exchange into articular cartilage and trigger bone remodelling. Ectopic lipid deposition in chondrocytes induced by dyslipidemia might initiate OA development, exacerbated by deregulated cellular lipid metabolism in joint tissues. Hyperglycaemia and OA interact at both local and systemic levels; local effects of oxidative stress and advanced glycation end-products are implicated in cartilage damage, whereas low-grade systemic inflammation results from glucose accumulation and contributes to a toxic internal environment that can exacerbate OA. Obesity-related metabolic factors, particularly altered levels of adipokines, contribute to OA development by inducing the expression of proinflammatory factors as well as degradative enzymes, leading to the inhibition of cartilage matrix synthesis and stimulation of subchondral bone remodelling. In this Review, we summarize the shared mechanisms of inflammation, oxidative stress, common metabolites and endothelial dysfunction that characterize the aetiologies of OA and MetS, and nominate metabolic OA as the fifth component of MetS. We also describe therapeutic opportunities that might arise from uniting these concepts.
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              The role of the chondrocyte in osteoarthritis.

              M Goldring (2000)
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                24 April 2015
                May 2015
                : 16
                : 5
                : 9341-9353
                Affiliations
                [1 ]Department of Physics, Norwegian University of Science and Technology (NTNU), N-7491 Trondheim, Norway; E-Mails: catharina.davies@ 123456ntnu.no (C.L.D.); magnus.lilledahl@ 123456ntnu.no (M.B.L.)
                [2 ]Physical Optics and Electronics Group, Massachusetts Institute of Technology (MIT), Cambridge, MA 02139, USA; E-Mail: gpsingh@ 123456mit.edu
                [3 ]Orthopaedic Department, Levanger Hospital, Kirkegata 2, N-7600 Levanger, Norway; E-Mail: kirstengroenhaug@ 123456gmail.com
                [4 ]Nofima, Postbox 210, N-1431 Ås, Norway; E-Mail: nils.kristian.afseth@ 123456nofima.no
                [5 ]Department of Orthopaedic Surgery, Trondheim University Hospital, N-7491 Trondheim, Norway; E-Mail: jon.o.drogset@ 123456ntnu.no
                Author notes
                [* ]Author to whom correspondence should be addressed; E-Mail: 101rajesh@ 123456gmail.com ; Tel.: +47-7359-3412; Fax: +47-7359-7710.
                Article
                ijms-16-09341
                10.3390/ijms16059341
                4463591
                25918938
                99887686-82a8-41e0-8dc6-a329372b2e3c
                © 2015 by the authors; licensee MDPI, Basel, Switzerland.

                This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 19 March 2015
                : 20 April 2015
                Categories
                Article

                Molecular biology
                raman spectroscopy,osteoarthritis,chondrocytes,biomedical optical diagnosis
                Molecular biology
                raman spectroscopy, osteoarthritis, chondrocytes, biomedical optical diagnosis

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