The expression of N-cadherin,fibronectin during chondrogenic differentiation of MSC induced by TGF-β1

被引:0
|
作者
李文革 [1 ]
徐莘香 [2 ]
机构
[1] Department of Orthopaedics, Peking University Zhenzhen Hospital, Shenzhen 518036,China
[2] Department of Orthopaedics,the First Clinical Hospital of Jilin University, Changchun 130021,China
关键词
Mesenchymal stem cells; Cell adhesion molecules; Condensation;
D O I
暂无
中图分类号
R68 [骨科学(运动系疾病、矫形外科学)];
学科分类号
1002 ; 100210 ;
摘要
Objective:To investigate the role of N-cadherin and fibronectin during chondrogenesis. Methods: Immunohistochemical method and autibody induced changes of aggregation of cells were used to assay the expressions of N-cadherin and fibronectin during cell differentiation. Results: The N-cadherin was present in the area of the cell nodular area in the 24 hours group after adding chondrogenic revulsant, then there was a down-regulating trend. Fibronectin was expressed in 48 and 72 hours groups after adding chondrogenic revulsant, and showed to be negative afterward. The antibody against fibronectin or N-cadherin could inhibit the formation of cellular nodule markedly. Conclusions: Cell adhesion factors play an important role during cell differentiation. TGF-β1 stimulates chondrogenesis via transition from an initial N-cadherin-contributing stage to a succedent fibronectin-contributing stage during the process of chondrogenesis in MSCs. Further study is needed to evaluate whether or not it can promote chondrogenesis by transfecting cDNA of CAMs to MSCs.
引用
收藏
页码:349 / 351
页数:3
相关论文
共 50 条
  • [11] N-Cadherin Mimetic Peptide Nanofiber System Induces Chondrogenic Differentiation of Mesenchymal Stem Cells
    Cimenci, Cagla Eren
    Kurtulus, Gozde Uzunalli
    Caliskan, Ozum S.
    Guler, Mustafa O.
    Tekinay, Ayse B.
    [J]. BIOCONJUGATE CHEMISTRY, 2019, 30 (09) : 2417 - 2426
  • [12] TGF-β1 Snail E-cadherin及N-cadherin在胃癌中的表达及意义
    祝迎锋
    吴继锋
    马伟
    张红
    王道斌
    [J]. 中国肿瘤临床, 2007, (24) : 1400 - 1404
  • [13] TGF-β3 inhibits chondrogenesis by suppressing precartilage condensation through stimulation of N-cadherin shedding and reduction of cRREB-1 expression
    Jin, Eun-Jung
    Park, Kwang Sook
    Kim, Dongkyun
    Lee, Young-Sup
    Sonn, Jong Kyung
    Jung, Jae Chang
    Bang, Ok-Sun
    Kang, Shin-Sung
    [J]. MOLECULES AND CELLS, 2010, 29 (04) : 425 - 432
  • [14] EXAMINATION OF N-CADHERIN AND ITS ASSOCIATED PROTEINS DURING NEURONAL DIFFERENTIATION
    KYPTA, RM
    MURPHYERDOSH, C
    REICHARDT, LF
    [J]. JOURNAL OF CELLULAR BIOCHEMISTRY, 1993, : 260 - 260
  • [15] TGF-β1, TGF-β receptor II and ED-A fibronectin expression in myofibroblast of vitreoretinopathy
    Bochaton-Piallat, ML
    Kapetanios, AD
    Donati, G
    Redard, M
    Gabbiani, G
    Pournaras, CJ
    [J]. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2000, 41 (08) : 2336 - 2342
  • [16] TGF-β1在乳腺癌中下调E-cadherin、上调N-cadherin和促进侵袭转移
    袁静萍
    袁修学
    陈创
    高利昆
    何惠华
    饶洁
    阎红琳
    [J]. 中国组织化学与细胞化学杂志, 2016, 25 (06) : 528 - 534
  • [17] Viral hepatitis is associated with intrahepatic cholangiocarcinoma with cholangiolar differentiation and N-cadherin expression
    Yu, Tsan-Hua
    Yuan, Ray-Hwang
    Chen, Yu-Ling
    Yang, Wan-Ching
    Hsu, Hey-Chi
    Jeng, Yung-Ming
    [J]. MODERN PATHOLOGY, 2011, 24 (06) : 810 - 819
  • [18] NONCOORDINATE DEVELOPMENTAL REGULATION OF N-CADHERIN, N-CAM, INTEGRIN, AND FIBRONECTIN MESSENGER-RNA LEVELS DURING MYOBLAST TERMINAL DIFFERENTIATION
    MACCALMAN, CD
    BARDEESY, N
    HOLLAND, PC
    BLASCHUK, OW
    [J]. DEVELOPMENTAL DYNAMICS, 1992, 195 (02) : 127 - 132
  • [19] N-CAM AND N-CADHERIN EXPRESSION DURING IN-VITRO CHONDROGENESIS
    TAVELLA, S
    RAFFO, P
    TACCHETTI, C
    CANCEDDA, R
    CASTAGNOLA, P
    [J]. EXPERIMENTAL CELL RESEARCH, 1994, 215 (02) : 354 - 362
  • [20] E/N-cadherin switch mediates cancer progression via TGF-β-induced epithelial-to-mesenchymal transition in extrahepatic cholangiocarcinoma
    Araki, K.
    Shimura, T.
    Suzuki, H.
    Tsutsumi, S.
    Wada, W.
    Yajima, T.
    Kobayahi, T.
    Kubo, N.
    Kuwano, H.
    [J]. BRITISH JOURNAL OF CANCER, 2011, 105 (12) : 1885 - 1893