Iksan526 Rice Callus Extract Induces Dedifferentiation of Rabbit Articular Chondrocytes via ERK1/2 and PI-3K/Akt Pathways

The resveratrol-enriched transgenic rice line Iksan526 (IS526), first developed by the Rural Development Administration of Korea using genetic engineering techniques, shows beneficial health effects in mitigating metabolic syndrome and obesity. However, the effects of IS526 on the differentiation of...

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Main Authors: Seong-Hui Eo, Song Ja Kim
Format: Article
Language:English
Published: Elsevier 2020-11-01
Series:Rice Science
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1672630820300809
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spelling doaj-4dd58b4a1592445fb1881cface453a0f2020-11-25T03:51:29ZengElsevierRice Science1672-63082020-11-01276504514Iksan526 Rice Callus Extract Induces Dedifferentiation of Rabbit Articular Chondrocytes via ERK1/2 and PI-3K/Akt PathwaysSeong-Hui Eo0Song Ja Kim1Department of Biological Sciences, College of Natural Sciences, Kongju National University, Gongju 32588, Republic of KoreaCorresponding author.; Department of Biological Sciences, College of Natural Sciences, Kongju National University, Gongju 32588, Republic of KoreaThe resveratrol-enriched transgenic rice line Iksan526 (IS526), first developed by the Rural Development Administration of Korea using genetic engineering techniques, shows beneficial health effects in mitigating metabolic syndrome and obesity. However, the effects of IS526 on the differentiation of chondrocytes and the underlying mechanism have not been investigated in detail. In this study, the effects and cellular regulatory mechanisms of IS526 on rabbit articular chondrocytes were examined. Following IS526 callus extract treatment, the expression levels of differentiation-related proteins were detected via western blotting, Alcian blue staining and immune-luorescence staining. IS526 decreased the type II collagen and proteoglycan levels in dose- and time-dependent manners. We further analyzed the effects of IS526 on skeleton genesis in zebrafish larvae using Alcian blue staining, which showed a reduction in cartilage formation along with increased production of matrix metalloproteinase (MMP)-13. IS526 also increased the phosphorylation of ERK1/2 and p38 kinase but inhibited the phosphorylation of Akt. Pharmacological inhibition of MMP-13 blocked the IS526-induced decrease in type II collagen levels. Inhibition of p38 kinase or PI-3K/Akt with SB203580 and LY294002 enhanced the suppression of type II collagen, but the blockage of ERK-1/2 by PD98059 rescued IS526-induced dedifferentiation. These results suggested that IS526 regulates type II collagen and MMP-13 expression via the ERK1/2 and PI-3K/Akt pathways in rabbit articular chondrocytes.http://www.sciencedirect.com/science/article/pii/S1672630820300809ricechondrocytetype II collagenmatrix metalloproteinase-13rice callus extract
collection DOAJ
language English
format Article
sources DOAJ
author Seong-Hui Eo
Song Ja Kim
spellingShingle Seong-Hui Eo
Song Ja Kim
Iksan526 Rice Callus Extract Induces Dedifferentiation of Rabbit Articular Chondrocytes via ERK1/2 and PI-3K/Akt Pathways
Rice Science
rice
chondrocyte
type II collagen
matrix metalloproteinase-13
rice callus extract
author_facet Seong-Hui Eo
Song Ja Kim
author_sort Seong-Hui Eo
title Iksan526 Rice Callus Extract Induces Dedifferentiation of Rabbit Articular Chondrocytes via ERK1/2 and PI-3K/Akt Pathways
title_short Iksan526 Rice Callus Extract Induces Dedifferentiation of Rabbit Articular Chondrocytes via ERK1/2 and PI-3K/Akt Pathways
title_full Iksan526 Rice Callus Extract Induces Dedifferentiation of Rabbit Articular Chondrocytes via ERK1/2 and PI-3K/Akt Pathways
title_fullStr Iksan526 Rice Callus Extract Induces Dedifferentiation of Rabbit Articular Chondrocytes via ERK1/2 and PI-3K/Akt Pathways
title_full_unstemmed Iksan526 Rice Callus Extract Induces Dedifferentiation of Rabbit Articular Chondrocytes via ERK1/2 and PI-3K/Akt Pathways
title_sort iksan526 rice callus extract induces dedifferentiation of rabbit articular chondrocytes via erk1/2 and pi-3k/akt pathways
publisher Elsevier
series Rice Science
issn 1672-6308
publishDate 2020-11-01
description The resveratrol-enriched transgenic rice line Iksan526 (IS526), first developed by the Rural Development Administration of Korea using genetic engineering techniques, shows beneficial health effects in mitigating metabolic syndrome and obesity. However, the effects of IS526 on the differentiation of chondrocytes and the underlying mechanism have not been investigated in detail. In this study, the effects and cellular regulatory mechanisms of IS526 on rabbit articular chondrocytes were examined. Following IS526 callus extract treatment, the expression levels of differentiation-related proteins were detected via western blotting, Alcian blue staining and immune-luorescence staining. IS526 decreased the type II collagen and proteoglycan levels in dose- and time-dependent manners. We further analyzed the effects of IS526 on skeleton genesis in zebrafish larvae using Alcian blue staining, which showed a reduction in cartilage formation along with increased production of matrix metalloproteinase (MMP)-13. IS526 also increased the phosphorylation of ERK1/2 and p38 kinase but inhibited the phosphorylation of Akt. Pharmacological inhibition of MMP-13 blocked the IS526-induced decrease in type II collagen levels. Inhibition of p38 kinase or PI-3K/Akt with SB203580 and LY294002 enhanced the suppression of type II collagen, but the blockage of ERK-1/2 by PD98059 rescued IS526-induced dedifferentiation. These results suggested that IS526 regulates type II collagen and MMP-13 expression via the ERK1/2 and PI-3K/Akt pathways in rabbit articular chondrocytes.
topic rice
chondrocyte
type II collagen
matrix metalloproteinase-13
rice callus extract
url http://www.sciencedirect.com/science/article/pii/S1672630820300809
work_keys_str_mv AT seonghuieo iksan526ricecallusextractinducesdedifferentiationofrabbitarticularchondrocytesviaerk12andpi3kaktpathways
AT songjakim iksan526ricecallusextractinducesdedifferentiationofrabbitarticularchondrocytesviaerk12andpi3kaktpathways
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