Inflammatory cell interations with surface-modified biomaterials

被引:0
作者
Anderson, James M. [1 ]
Jones, Jacqueline A. [1 ]
机构
[1] Case Western Reserve Univ, Dept Pathol, Cleveland, OH 44106 USA
来源
2007 INTERNATIONAL FORUM ON BIOMEDICAL TEXTILE MATERIALS, PROCEEDINGS | 2007年
关键词
biomaterials; inflammatory cells; foreign body reaction; macrophages; cell culture;
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Implantation of biomedical polymers, devices, and prostheses results in the normal sequence of inflammatory and wound healing events, ultimately resulting in the foreign body reaction at the tissue/material interface. The normal foreign body reaction consists of adherent macrophages and foreign body giant cells at the tissue/material interface. Our studies have focused on developing a mechanistic understanding of the effect of biomaterial surface chemistry on the formation and activity of monocytes, macrophages, lymphocytes, and foreign body giant cells in the foreign body reaction. Studies utilizing materials with a broad range of surface chemistries have been used to investigate the capability of surfaces to enhance or reduce macrophage and foreign body giant cell adhesion, fusion, activation, and apoptosis. Correlative in vitro and in vivo studies will be presented that identify certain surface chemistries that facilitate a reduction in the foreign body reaction while others enhance the foreign body reaction at material/tissue interfaces. Our ultimate goal is to identify biological design criteria that will prove useful in the development of new biomaterials and tissue engineering constructs.
引用
收藏
页码:197 / 200
页数:4
相关论文
共 12 条
[1]   In vivo leukocyte cytokine mRNA responses to biomaterials are dependent on surface chemistry [J].
Brodbeck, WG ;
Voskerician, G ;
Ziats, NP ;
Nakayama, Y ;
Matsuda, T ;
Anderson, JM .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2003, 64A (02) :320-329
[2]   Biomaterial adherent macrophage apoptosis is increased by hydrophilic and anionic substrates in vivo [J].
Brodbeck, WG ;
Patel, J ;
Voskerician, G ;
Christenson, E ;
Shive, MS ;
Nakayama, Y ;
Matsuda, T ;
Ziats, NP ;
Anderson, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (16) :10287-10292
[3]   Biomaterial surface chemistry dictates adherent monocyte/macrophage cytokine expression in vitro [J].
Brodbeck, WG ;
Nakayama, Y ;
Matsuda, T ;
Colton, E ;
Ziats, NP ;
Anderson, JM .
CYTOKINE, 2002, 18 (06) :311-319
[4]   Interleukin-4 inhibits tumor necrosis factor-α-induced and spontaneous apoptosis of biomaterial-adherent macrophages [J].
Brodbeck, WG ;
Shive, MS ;
Colton, E ;
Ziats, NP ;
Anderson, JM .
JOURNAL OF LABORATORY AND CLINICAL MEDICINE, 2002, 139 (02) :90-100
[5]  
Brodbeck WG, 2001, J BIOMED MATER RES, V55, P661, DOI 10.1002/1097-4636(20010615)55:4<661::AID-JBM1061>3.0.CO
[6]  
2-F
[7]   Surface chemistry mediates adhesive structure, cytoskeletal organization, and fusion of macrophages [J].
Dadsetan, M ;
Jones, JA ;
Hiltner, A ;
Anderson, JM .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2004, 71A (03) :439-448
[8]  
DeFife KM, 1999, J BIOMED MATER RES, V45, P148, DOI 10.1002/(SICI)1097-4636(199905)45:2<148::AID-JBM10>3.0.CO
[9]  
2-U
[10]  
JONES AJ, 2007, IN PRESS J BIOMED MA, pA81