Macrophage polarization: An opportunity for improved outcomes in and regenerative medicine

被引:733
作者
Brown, Bryan N. [1 ,2 ]
Ratner, Buddy D. [3 ,4 ]
Goodman, Stuart B. [5 ,6 ]
Amar, Salomon [7 ]
Badylak, Stephen F. [1 ,2 ,8 ]
机构
[1] Univ Pittsburgh, McGowan Inst Regenerat Med, Pittsburgh, PA 15218 USA
[2] Univ Pittsburgh, Dept Bioengn, Pittsburgh, PA 15218 USA
[3] Univ Washington, Dept Bioengn, Seattle, WA 98195 USA
[4] Univ Washington, Dept Chem Engn, Seattle, WA 98195 USA
[5] Stanford Univ, Dept Orthopaed Surg, Stanford, CA 94305 USA
[6] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[7] Boston Univ, Ctr Antiinflammatory Therapeut, Boston, MA 02215 USA
[8] Univ Pittsburgh, Dept Surg, Pittsburgh, PA 15218 USA
关键词
Foreign body response; Leukocyte; Macrophage; Biocompatibility; TUMOR-ASSOCIATED MACROPHAGES; NECROSIS-FACTOR-ALPHA; HUMAN PERIPHERAL-BLOOD; FOREIGN-BODY REACTION; SPINAL-CORD-INJURY; INSULIN-RESISTANCE; SKELETAL-MUSCLE; MUSCULAR-DYSTROPHY; ADIPOSE-TISSUE; PPAR-GAMMA;
D O I
10.1016/j.biomaterials.2012.02.034
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
The host response to biomaterials has been studied for decades. Largely, the interaction of host immune cells, macrophages in particular, with implanted materials has been considered to be a precursor to granulation tissue formation, the classic foreign body reaction, and eventual encapsulation with associated negative impacts upon device functionality. However, more recently, it has been shown that macrophages, depending upon context dependent polarization profiles, are capable of affecting both detrimental and beneficial outcomes in a number of disease processes and in tissue remodeling following injury. Herein, the diverse roles played by macrophages in these processes are discussed in addition to the potential manipulation of macrophage effector mechanisms as a strategy for promoting site-appropriate and constructive tissue remodeling as opposed to deleterious persistent inflammation and scar tissue formation. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3792 / 3802
页数:11
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