Supplemented Chondroitin Sulfate and Hyaluronic Acid Suppress Mineralization of the Chondrogenic Cell Line, ATDC5, via Direct Inhibition of Alkaline Phosphatase

被引:17
|
作者
Kudo, Toshiya [1 ]
Nakatani, Sachie [1 ]
Kakizaki, Misato [1 ]
Arai, Ai [1 ]
Ishida, Keisuke [1 ]
Wada, Masahiro [1 ]
Kobata, Kenji [1 ]
机构
[1] Josai Univ, Dept Pharmaceut Sci, 1-1 Keyakidai, Sakado, Saitama 3500295, Japan
关键词
chondroitin sulfate; chondrocyte; alkaline phosphatase; mineralization; ARTICULAR-CARTILAGE; DIFFERENTIATION; CHONDROCYTE; BONE; CALCIFICATION; LOCALIZATION; MECHANISM; AGGRECAN; RESIDUES; BINDING;
D O I
10.1248/bpb.b17-00059
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Chondroitin sulfate (CS) is a sulfated polysaccharide produced by chondrocytes. Alkaline phosphatase (ALP) is an important enzyme involved in the mineralization of chondrocytes. In recent years, it has been reported that CS regulates the differentiation of various cells. In this study, we investigated the effect of supplemented CS on ALP activity and mineralization of the chondrogenic cell line, ATDC5. In addition, hyaluronic acid (HA), a non-sulfated and acidic polysaccharide, was used in comparison to CS. CS and HA significantly suppressed ALP activity without affecting ATDC5 cell proliferation. In addition, although the inhibition of ALP activity was observed at every time point, Alp mRNA expression level was not affected by CS. The suppressive effect of CS on ALP activity was abrogated by pre-treatment with chondroitinase ABC (CSase). CS and L-homoarginine (hArg), an inhibitor of ALP, significantly suppressed mineralization in ATDC5 cells. In conclusion, supplemented CS directly inhibits ALP to prevent the progression of chondrocytes from differentiation to mineralization.
引用
收藏
页码:2075 / 2080
页数:6
相关论文
共 5 条
  • [1] Cellular hypertrophy and mineralization of mouse chondrogenic cell line ATDC5 in vitro
    Shukunami, C
    Ohta, Y
    Ishizeki, K
    Suzuki, F
    Hiraki, Y
    MATRIX BIOLOGY, 1997, 16 (02) : 77 - 78
  • [2] High Molecular Weight Hyaluronic Acid Increases the Differentiation Potential of the Murine Chondrocytic ATDC5 Cell Line
    Sato, Eiichi
    Ando, Takashi
    Ichikawa, Jiro
    Okita, Genki
    Sato, Nobutaka
    Wako, Masanori
    Ohba, Tetsuro
    Ochiai, Satoshi
    Hagino, Tetsuo
    Jacobson, Richard
    Haro, Hirotaka
    JOURNAL OF ORTHOPAEDIC RESEARCH, 2014, 32 (12) : 1619 - 1627
  • [3] Sustained phosphorylation of mutated FGFR3 is a crucial feature of genetic dwarfism and induces apoptosis in the ATDC5 chondrogenic cell line via PLCγ-activated STATI
    Harada, Daisuke
    Yamanaka, Yoshitaka
    Ueda, Koso
    Nishimura, Riko
    Morishima, Tsuneo
    Seino, Yoshiki
    Tanaka, Hiroyuki
    BONE, 2007, 41 (02) : 273 - 281
  • [4] The effect of lentivirus-mediated SIRT1 gene knockdown in the ATDC5 cell line via inhibition of the Wnt signaling pathway
    Yu, Fei
    Yuan, Yusong
    Li, Dongdong
    Kou, Yuhui
    Jiang, Baoguo
    Zhang, Peixun
    CELLULAR SIGNALLING, 2019, 53 : 80 - 89
  • [5] TGF-β1 inhibits maturation of chondrogenic cell line ATDC5 by impeding canonical hedgehog signaling through direct down-regulation of ciliary component gene Ift88
    Kawasaki, Makiri
    Nakamoto, Tetsuya
    Notomi, Takuya
    Hayata, Tadayoshi
    Ezura, Yoichi
    Noda, Masaki
    JOURNAL OF BONE AND MINERAL RESEARCH, 2013, 28