Effects of Sulforaphane on Human Chondrocytes Cultured In Vitro

被引:1
作者
Zhu Weimin [1 ,2 ,3 ,4 ,5 ]
Chen Jie-Lin [1 ,2 ]
Cui Jiaming [1 ,2 ,3 ,4 ,5 ]
Huang Jianghong [1 ,2 ]
Xiong Jianyi [1 ,2 ,3 ]
Duan Li [1 ,2 ]
Wang Daping [1 ,2 ,3 ,4 ,5 ]
机构
[1] Shenzhen Second Peoples Hosp, Shenzhen Key Lab Tissue Engn, Shenzhen 518035, Guangdong, Peoples R China
[2] Shenzhen Ctr Sports Med & Engn Technol, Shenzhen 518035, Guangdong, Peoples R China
[3] Guangzhou Med Univ, Guangzhou 510182, Guangdong, Peoples R China
[4] Shenzhen Univ, Shenzhen Key Lab Antiaging & Regenerat Med, Shenzhen 518060, Guangdong, Peoples R China
[5] Chinese Orthopaed Regenerat Med Grp, Hangzhou 310000, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Sulforaphane; SOX-9; MMP-13; Chondrocytes; ARTICULAR CHONDROCYTES; GENE-EXPRESSION; CARTILAGE; OSTEOARTHRITIS; COLLAGEN; CANCER; APOPTOSIS; PROTEASES; PROFILES; AGGRECAN;
D O I
10.1166/jbt.2016.1552
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Chondrocyte dedifferentiation is the one of the major factors that affect the clinic outcomes of autologous chondrocyte implantation (ACI) for cartilage repair due to fibrocartilage formation. Molecules in the extracellular matrix (ECM) like type II collagen and proteoglycans play a key role in the quality of newly-formed cartilage. Sulforaphane (SFN), as a plant-derived compound, was investigated for its effects on human chondrocyte cultured in vitro in the present study. We showed a concentration of 8 mu M SFN would change the expression pattern of the ECM molecules of chondrocyte, with the increased ratio of type II collagen/type I collagen, increased expression of SOX9, BMP2 and decreased expression of matrix metallopeptidase 13 (MMP13). The change of the gene expression level would benefit for the inhibition of chondrocyte dedifferentiation in vitro, thus helping hyaline cartilage regeneration after ACI surgery. However, microarray analysis revealed expressions of gene clusters relating to cell proliferation and growth significantly changed and cell number decreased after SFN treatment, suggesting its negative role in chondrocyte expansion. Therefore, optimizing SFN concentration and the culture time might be a promising way for chondrocyte culture for clinic use.
引用
收藏
页码:998 / 1005
页数:8
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