Cultured articular chondrocytes sheets for partial thickness cartilage defects utilizing temperature-responsive culture dishes

被引:34
作者
Kaneshiro, N.
Sato, M.
Ishihara, M.
Mitani, G.
Sakai, H.
Kikuchi, T.
Mochida, J.
机构
[1] Tokai Univ, Sch Med, Dept Orthopaed Surg, Isehara, Kanagawa 2591193, Japan
[2] Natl Def Med Coll, Dept Med Engn, Tokorozawa, Saitama 3598513, Japan
[3] CellSeed Inc, Shinjuku Ku, Tokyo 1620056, Japan
关键词
cell sheet; cultured cell; articular cartilage; partial thickness defect; chondrocyte; temperature-responsive culture dish;
D O I
10.22203/eCM.v013a09
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The extracellular matrix ( ECM) of articular cartilage has several functions that are unique to joints. Although a technique for transplanting cultured chondrocytes has already been introduced, it is difficult to collect intact ECM when using enzymes to harvest samples. Temperature-responsive culture dishes have already been clinically applied in the fields of myocardial and corneal transplantation. Earlier studies have shown that a sheet of cultured cells with intact ECM and adhesive factors can be harvested using such culture dishes, which allow the surface properties of the dish to be reversibly altered by changing the temperature. Human chondrocytes were subjected to enzymatic digestion and then were seeded in temperature-responsive culture dishes. A sheet of chondrocytes was harvested by only reducing the temperature after the cultured cells reached confluency. A real-time PCR analysis of the chondrocyte sheets confirmed that type II collagen, aggrecan, and fibronectin were present. These results suggested that, although chondrocytes undergo dedifferentiation in a monolayer culture, multilayer chondrocyte sheets grown in a similar environment to that of three-dimensional culture may be able to maintain a normal phenotype. A histological examination suggested that multilayer chondrocyte sheets could thus prevent the loss of proteoglycans because the area covered by the sheets was well stained by safranin-O. The present experiments suggested that temperature-responsive culture dishes are useful for obtaining cultured chondrocytes, which may then be clinically employed as a substitute for periosteal patches because such sheets can be applied without a scaffold.
引用
收藏
页码:87 / 92
页数:6
相关论文
共 21 条
  • [1] TREATMENT OF DEEP CARTILAGE DEFECTS IN THE KNEE WITH AUTOLOGOUS CHONDROCYTE TRANSPLANTATION
    BRITTBERG, M
    LINDAHL, A
    NILSSON, A
    OHLSSON, C
    ISAKSSON, O
    PETERSON, L
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (14) : 889 - 895
  • [2] Novel approach for achieving double-layered cell sheets co-culture: overlaying endothelial cell sheets onto monolayer hepatocytes utilizing temperature-responsive culture dishes
    Harimoto, M
    Yamato, M
    Hirose, M
    Takahashi, C
    Isoi, Y
    Kikuchi, A
    Okano, T
    [J]. JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 2002, 62 (03): : 464 - 470
  • [3] Creation of designed shape cell sheets that are noninvasively harvested and moved onto another surface
    Hirose, M
    Kwon, OH
    Yamato, M
    Kikuchi, A
    Okano, T
    [J]. BIOMACROMOLECULES, 2000, 1 (03) : 377 - 381
  • [4] Two-dimensional manipulation of confluently cultured vascular endothelial cells using temperature-responsive poly(N-isopropylacrylamide)-grafted surfaces
    Kikuchi, A
    Okuhara, M
    Karikusa, F
    Sakurai, Y
    Okano, T
    [J]. JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 1998, 9 (12) : 1331 - 1348
  • [5] Kushida A, 2000, J BIOMED MATER RES, V51, P216, DOI 10.1002/(SICI)1097-4636(200008)51:2<216::AID-JBM10>3.0.CO
  • [6] 2-K
  • [7] Kushida A, 1999, J BIOMED MATER RES, V45, P355, DOI 10.1002/(SICI)1097-4636(19990615)45:4<355::AID-JBM10>3.0.CO
  • [8] 2-7
  • [9] ARTHROSCOPIC MULTIPLE OSTEOCHONDRAL TRANSPLANTATION TO THE CHONDRAL DEFECT IN THE KNEE ASSOCIATED WITH ANTERIOR CRUCIATE LIGAMENT DISRUPTION
    MATSUSUE, Y
    YAMAMURO, T
    HAMA, H
    [J]. ARTHROSCOPY, 1993, 9 (03): : 318 - 321
  • [10] Corneal reconstruction with tissue-engineered cell sheets composed of autologous oral mucosal epithelium
    Nishida, K
    Yamato, M
    Hayashida, Y
    Watanabe, K
    Yamamoto, K
    Adachi, E
    Nagai, S
    Kikuchi, A
    Maeda, N
    Watanabe, H
    Okano, T
    Tano, Y
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (12) : 1187 - 1196