Effects of hedgehog proteins on tissue engineering of cartilage in vitro

被引:18
|
作者
Kellner, K
Lang, K
Papadimitriou, A
Leser, U
Milz, S
Schulz, MB
Blunk, T
Göpferich, A [1 ]
机构
[1] Univ Regensburg, Dept Pharmaceut Technol, D-93040 Regensburg, Germany
[2] Roche Pharma Res, Penzberg, Germany
[3] Univ Munich, Inst Anat, Munich, Germany
来源
TISSUE ENGINEERING | 2002年 / 8卷 / 04期
关键词
D O I
10.1089/107632702760240481
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The effects of three derivatives of the N-terminal signaling domain of hedgehog proteins on cartilage engineered in vitro were investigated, with specific focus on the ability to increase tissue growth rate and concentrations of major extracellular matrix components, that is, glycosaminoglycans (GAG) and collagen, and on the effects on morphological appearance of the tissue. Bovine articular chondrocytes were cultured on biodegradable polyglycolic acid (PGA) scaffolds with or without the addition of dipalmitoylated sonic hedgehog (dp-shh), dipalmitoylated indian hedgehog (dp-ihh), or sonic hedgehog dimer (shh-dimer) to medium with either 1% or 10 % fetal bovine serum (FBS). All three hedgehog proteins dose-dependently increased construct weights (by up to 1.95-fold, dp-shh at 1,000 ng/mL) and the fraction of GAG over 4 weeks (by up to 2.7-fold, dp-shh at 1,000 ng/mL), as compared to control constructs. Dp-shh and dp-ihh elicited similar responses; a 10-fold higher concentration of nonacylated shh-dimer was necessary to reach comparable results. Positive hedgehog effects were more pronounced in medium containing I % FBS than in medium containing 10% FBS; however, at either FBS concentration, cartilaginous tissues grown in the presence of hedgehog proteins appeared morphologically more mature. Hedgehog derivatives thus appear as promising candidates to improve the development and composition of engineered cartilage.
引用
收藏
页码:561 / 572
页数:12
相关论文
共 50 条
  • [1] The Effects of Extracellular Matrix on Tissue Engineering Construction of Cartilage in Vitro
    YU Li~ 1
    ChineseJournalofBiomedicalEngineering(EnglishEdition), 2006, (02) : 88 - 92
  • [2] Tissue engineering:: advances in in vitro cartilage generation
    Risbud, MV
    Sittinger, M
    TRENDS IN BIOTECHNOLOGY, 2002, 20 (08) : 351 - 356
  • [3] Extracellular matrix production in vitro in cartilage tissue engineering
    Jie-Lin Chen
    Li Duan
    Weimin Zhu
    Jianyi Xiong
    Daping Wang
    Journal of Translational Medicine, 12
  • [4] Extracellular matrix production in vitro in cartilage tissue engineering
    Chen, Jie-Lin
    Duan, Li
    Zhu, Weimin
    Xiong, Jianyi
    Wang, Daping
    JOURNAL OF TRANSLATIONAL MEDICINE, 2014, 12
  • [5] TISSUE ENGINEERING IN AN IN VITRO MODEL OF HUMAN CARTILAGE REPAIR
    Sanjurjo Rodriguez, C.
    Castro Vinuelas, R.
    Hermida Gomez, T.
    Fuentes Boquete, I.
    De Toro Santos, F.
    Blanco Garcia, F.
    Diaz Prado, S.
    OSTEOARTHRITIS AND CARTILAGE, 2016, 24 : S169 - S170
  • [6] Insights into in vitro environments for human cartilage tissue engineering
    Abraham, Samuel J. K.
    Yoshioka, Hiroshi
    INDIAN JOURNAL OF MEDICAL RESEARCH, 2016, 144 : 796 - 798
  • [7] The effects of physical forces on cartilage tissue engineering
    Heath, CA
    BIOTECHNOLOGY & GENETIC ENGINEERING REVIEWS, VOL 17, 2000, 17 : 533 - 551
  • [8] Tissue engineering for cartilage repair: in vitro development of an osteochondral scaffold
    Deponti, D.
    Di, Giancamillo A.
    Gervaso, F.
    Pozzi, A.
    Ballis, R.
    Scalera, F.
    Domenicucci, M.
    Domeneghini, C.
    Sannino, A.
    Peretti, G. M.
    JOURNAL OF TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2012, 6 : 155 - 155
  • [9] Engineering functional cartilage and cardiac tissue:: In vitro culture parameters
    Freed, LE
    Rupnick, MA
    Schaefer, D
    Vunjak-Novakovic, G
    FUNCTIONAL TISSUE ENGINEERING, 2003, : 360 - 376
  • [10] In vitro model systems for tissue engineering of cartilage and intervertebral disc
    Roberts, S
    Gargiulo, B
    Evans, EH
    Menage, J
    Johnson, WEB
    Eisenstein, S
    Richardson, JB
    INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY, 2005, 86 (03) : A42 - A42