Effect of <i>Rubus idaeus</i> Extracts in Murine Chondrocytes and Explants

Osteoarthritis is characterized by cartilage loss resulting from the activation of chondrocytes associated with a synovial inflammation. Activated chondrocytes promote an increased secretion of matrix proteases and proinflammatory cytokines leading to cartilage breakdown. Since natural products poss...

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Main Authors: Morgane Bourmaud, Mylene Zarka, Romain Le Cozannet, Pascale Fança-Berthon, Eric Hay, Martine Cohen-Solal
Format: Article
Language:English
Published: MDPI AG 2021-02-01
Series:Biomolecules
Subjects:
Online Access:https://www.mdpi.com/2218-273X/11/2/245
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author Morgane Bourmaud
Mylene Zarka
Romain Le Cozannet
Pascale Fança-Berthon
Eric Hay
Martine Cohen-Solal
author_facet Morgane Bourmaud
Mylene Zarka
Romain Le Cozannet
Pascale Fança-Berthon
Eric Hay
Martine Cohen-Solal
author_sort Morgane Bourmaud
collection DOAJ
description Osteoarthritis is characterized by cartilage loss resulting from the activation of chondrocytes associated with a synovial inflammation. Activated chondrocytes promote an increased secretion of matrix proteases and proinflammatory cytokines leading to cartilage breakdown. Since natural products possess anti-inflammatory properties, we investigated the direct effect of <i>Rubus idaeus</i> extracts (RIE) in chondrocyte metabolism and cartilage loss. The effect of RIE in chondrocyte metabolism was analyzed in murine primary chondrocytes and cartilage explants. We also assessed the contribution of RIE in an inflammation environment by culturing mice primary chondrocytes with the supernatant of Raw 264.7 macrophage-like cells primed with RIE. In primary chondrocytes, RIE diminished chondrocyte hypertrophy (<i>Col10</i>), while increasing the expression of catabolic genes (<i>Mmp-3</i>, <i>Mmp-13)</i> and reducing anabolic genes (<i>Col2a1</i>, <i>Acan</i>). In cartilage explants, <i>Rubus idaeus</i> prevented the loss of proteoglycan (14.84 ± 3.07% loss of proteoglycans with IL1 alone vs. 3.03 ± 1.86% with IL1 and 100 µg/mL of RIE), as well as the NITEGE neoepitope expression. RIE alone reduced the expression of <i>Il1</i> and <i>Il6</i> in macrophages, without changes in <i>Tnf</i> and <i>Cox2</i> expression. The secretome of macrophages pre-treated with RIE and transferred to chondrocytes decreases the gene and protein expression of <i>Mmp-3</i> and <i>Cox2</i>. In conclusion, these data suggest that RIE may protect from chondrocyte catabolism and cartilage loss in inflammatory conditions. Further evaluations are need before considering RIE as a candidate for the treatment for osteoarthritis.
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spelling doaj.art-a9b78682160f4e49a48fc1e8b2eef06f2023-12-03T12:58:10ZengMDPI AGBiomolecules2218-273X2021-02-0111224510.3390/biom11020245Effect of <i>Rubus idaeus</i> Extracts in Murine Chondrocytes and ExplantsMorgane Bourmaud0Mylene Zarka1Romain Le Cozannet2Pascale Fança-Berthon3Eric Hay4Martine Cohen-Solal5BIOSCAR Inserm U1132, Department of Rheumatology, Université de Paris, Hôpital Lariboisière, F-75010 Paris, FranceBIOSCAR Inserm U1132, Department of Rheumatology, Université de Paris, Hôpital Lariboisière, F-75010 Paris, FranceNaturex, Part of Givaudan SA, 250 rue Pierre Bayle, 84000 Avignon, FranceNaturex, Part of Givaudan SA, 250 rue Pierre Bayle, 84000 Avignon, FranceBIOSCAR Inserm U1132, Department of Rheumatology, Université de Paris, Hôpital Lariboisière, F-75010 Paris, FranceBIOSCAR Inserm U1132, Department of Rheumatology, Université de Paris, Hôpital Lariboisière, F-75010 Paris, FranceOsteoarthritis is characterized by cartilage loss resulting from the activation of chondrocytes associated with a synovial inflammation. Activated chondrocytes promote an increased secretion of matrix proteases and proinflammatory cytokines leading to cartilage breakdown. Since natural products possess anti-inflammatory properties, we investigated the direct effect of <i>Rubus idaeus</i> extracts (RIE) in chondrocyte metabolism and cartilage loss. The effect of RIE in chondrocyte metabolism was analyzed in murine primary chondrocytes and cartilage explants. We also assessed the contribution of RIE in an inflammation environment by culturing mice primary chondrocytes with the supernatant of Raw 264.7 macrophage-like cells primed with RIE. In primary chondrocytes, RIE diminished chondrocyte hypertrophy (<i>Col10</i>), while increasing the expression of catabolic genes (<i>Mmp-3</i>, <i>Mmp-13)</i> and reducing anabolic genes (<i>Col2a1</i>, <i>Acan</i>). In cartilage explants, <i>Rubus idaeus</i> prevented the loss of proteoglycan (14.84 ± 3.07% loss of proteoglycans with IL1 alone vs. 3.03 ± 1.86% with IL1 and 100 µg/mL of RIE), as well as the NITEGE neoepitope expression. RIE alone reduced the expression of <i>Il1</i> and <i>Il6</i> in macrophages, without changes in <i>Tnf</i> and <i>Cox2</i> expression. The secretome of macrophages pre-treated with RIE and transferred to chondrocytes decreases the gene and protein expression of <i>Mmp-3</i> and <i>Cox2</i>. In conclusion, these data suggest that RIE may protect from chondrocyte catabolism and cartilage loss in inflammatory conditions. Further evaluations are need before considering RIE as a candidate for the treatment for osteoarthritis.https://www.mdpi.com/2218-273X/11/2/245<i>Rubus idaeus</i>chondrocytesmacrophagesosteoarthritisinflammation
spellingShingle Morgane Bourmaud
Mylene Zarka
Romain Le Cozannet
Pascale Fança-Berthon
Eric Hay
Martine Cohen-Solal
Effect of <i>Rubus idaeus</i> Extracts in Murine Chondrocytes and Explants
Biomolecules
<i>Rubus idaeus</i>
chondrocytes
macrophages
osteoarthritis
inflammation
title Effect of <i>Rubus idaeus</i> Extracts in Murine Chondrocytes and Explants
title_full Effect of <i>Rubus idaeus</i> Extracts in Murine Chondrocytes and Explants
title_fullStr Effect of <i>Rubus idaeus</i> Extracts in Murine Chondrocytes and Explants
title_full_unstemmed Effect of <i>Rubus idaeus</i> Extracts in Murine Chondrocytes and Explants
title_short Effect of <i>Rubus idaeus</i> Extracts in Murine Chondrocytes and Explants
title_sort effect of i rubus idaeus i extracts in murine chondrocytes and explants
topic <i>Rubus idaeus</i>
chondrocytes
macrophages
osteoarthritis
inflammation
url https://www.mdpi.com/2218-273X/11/2/245
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AT pascalefancaberthon effectofirubusidaeusiextractsinmurinechondrocytesandexplants
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