Adhesion behavior of monocytes, macrophages and foreign body giant cells on poly (N-isopropylacrylamide) temperature-responsive surfaces

被引:34
作者
Collier, TO
Anderson, JM
Kikuchi, A
Okano, T
机构
[1] Case Western Reserve Univ, Dept Macromol Sci, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Inst Pathol, Cleveland, OH 44106 USA
[3] Tokyo Womens Med Univ, Inst Biomed Engn, Tokyo, Japan
来源
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH | 2002年 / 59卷 / 01期
关键词
monocytes; macrophage adhesions; foreign body giant cell (FBGC) formation; temperature-responsive surfaces;
D O I
10.1002/jbm.1225
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Monocyte and macrophage adhesion and foreign body giant cell (FBGC) formation has been observed on surfaces with a wide range of properties. In this study we have utilized novel, temperature-responsive surfaces (TRS) with dynamic surface properties to investigate inflammatory cell adhesion behavior. With temperature changes, grafted chains of poly-N-isopropylacrylamide pass through their lower critical solution temperature (LCST) and can either extend (hydrate), creating a hydrophilic surface at 20 degreesC, or contract (dehydrate), creating a hydrophobic surface at 37 degreesC. Isolated human monocytes and monocyte-derived macrophages were able to adhere, spread, and form FBGC on the hydrophobic surface. Decreasing the temperature below the lower critical solution temperature induced a change in the surface wettability, creating a hydrophilic surface, that induced a differential detachment of adherent cells that decreased with time, ranging from 98% after 2 h of culture to 30% at day 10. These detached cells remained viable, and were recultured onto TCPS for 3, 7, and 10 days. These novel surfaces allow investigation of the adhesive behavior of adherent inflammatory cells in a temporal manner, and the effects of surface conformation and wettability changes on cell adhesion and detachment. (C) 2001 John Wiley & Sons, Inc.
引用
收藏
页码:136 / 143
页数:8
相关论文
共 46 条
  • [1] Monocyte, macrophage and foreign body giant cell interactions with molecularly engineered surfaces
    Anderson, JM
    Defife, K
    Mcnally, A
    Collier, T
    Jenney, C
    [J]. JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 1999, 10 (10-11) : 579 - 588
  • [2] ANDERSON JM, 1984, BIOMATERIALS, V5, P5, DOI 10.1016/0142-9612(84)90060-7
  • [3] Integrin signalling in neutrophils and macrophages
    Berton, G
    Lowell, CA
    [J]. CELLULAR SIGNALLING, 1999, 11 (09) : 621 - 635
  • [4] Brodbeck WG, 2001, J BIOMED MATER RES, V55, P661, DOI 10.1002/1097-4636(20010615)55:4<661::AID-JBM1061>3.0.CO
  • [5] 2-F
  • [6] PROTEIN ADSORPTION AND ENDOTHELIAL-CELL ATTACHMENT AND PROLIFERATION ON PAPI-BASED ADDITIVE MODIFIED POLY(ETHER URETHANE UREAS)
    BRUNSTEDT, MR
    ZIATS, NP
    SCHUBERT, M
    STACK, S
    ROSECAPRARA, V
    HILTNER, PA
    ANDERSON, JM
    [J]. JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1993, 27 (04): : 499 - 510
  • [7] CYTOKINES AND MACROPHAGES
    CAVAILLON, JM
    [J]. BIOMEDICINE & PHARMACOTHERAPY, 1994, 48 (10) : 445 - 453
  • [8] Cellular control lies in the balance of forces
    Chicurel, ME
    Chen, CS
    Ingber, DE
    [J]. CURRENT OPINION IN CELL BIOLOGY, 1998, 10 (02) : 232 - 239
  • [9] Collier TO, 2000, J BIOMED MATER RES, V49, P141, DOI 10.1002/(SICI)1097-4636(200001)49:1<141::AID-JBM18>3.0.CO
  • [10] 2-A