Development of optical probes for in vivo imaging of polarized macrophages during foreign body reactions

被引:24
作者
Baker, David W. [1 ]
Zhou, Jun [1 ]
Tsai, Yi-Ting [1 ]
Patty, Kaitlen M. [1 ]
Weng, Hong [1 ]
Tang, Ewin N. [1 ]
Nair, Ashwin [1 ]
Hu, Wen-Jing [2 ]
Tang, Liping [1 ,3 ]
机构
[1] Univ Texas Arlington, Dept Bioengn, Arlington, TX 76019 USA
[2] Progenitec Inc, Arlington, TX 76001 USA
[3] Kaohsiung Med Univ, Dept Biomed Sci & Environm Biol, Kaohsiung 807, Taiwan
基金
美国国家卫生研究院;
关键词
Macrophage polarization; In vivo imaging; Optical probe; Inflammation; Biomaterials; ACTIVATED MACROPHAGES; INFLAMMATORY RESPONSES; MURINE MACROPHAGES; ALTERNATIVE ACTIVATION; MANNOSYLATED LIPOSOMES; IFN-GAMMA; CELLS; ARTHRITIS; VITRO; NANOPARTICLES;
D O I
10.1016/j.actbio.2014.04.001
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Plasticity of macrophage (MO) phenotypes exist in a spectrum from classically activated (M1) cells, to alternatively activated (M2) cells, contributing to both the normal healing of tissues and the pathogenesis of implant failure. Here, folate- and mannose-based optical probes were fabricated to simultaneously determine the degree of MO polarization. In vitro tests show the ability of these probes to specifically target M1 and M2 cells. In an in vivo murine model, they were able to distinguish between the M1-dominated inflammatory response to infection and the M2-dominated regenerative response to particle implants. Finally, the probes were used to assess the inflammatory/regenerative properties of biomaterial implants. Our results show that these probes can be used to monitor and quantify the dynamic processes of MO polarization and their role in cellular responses in real time. (C) 2014 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:2945 / 2955
页数:11
相关论文
共 61 条
[1]  
ANDERSON JM, 1993, CARDIOVASC PATHOL, V2, pS33
[2]   Increased uptake of folate conjugates by activated macrophages in experimental hyperlipemia [J].
Antohe, F ;
Radulescu, L ;
Puchianu, E ;
Kennedy, MD ;
Low, PS ;
Simionescu, M .
CELL AND TISSUE RESEARCH, 2005, 320 (02) :277-285
[3]   Role of IFN-γ in regulating development of alternatively T2 immunity and the activated macrophages during allergic bronchopulmonary mycosis [J].
Arora, S ;
Hernandez, Y ;
Erb-Downward, JR ;
McDonald, RA ;
Toews, GB ;
Huffnagle, GB .
JOURNAL OF IMMUNOLOGY, 2005, 174 (10) :6346-6356
[4]   Effect of Cytokine Interplay on Macrophage Polarization during Chronic Pulmonary Infection with Cryptococcus neoformans [J].
Arora, Shikha ;
Olszewski, Michal A. ;
Tsang, Tiffany M. ;
McDonald, Roderick A. ;
Toews, Galen B. ;
Huffnagle, Gary B. .
INFECTION AND IMMUNITY, 2011, 79 (05) :1915-1926
[5]   Macrophage Phenotype as a Determinant of Biologic Scaffold Remodeling [J].
Badylak, Stephen F. ;
Valentin, Jolene E. ;
Ravindra, Anjani K. ;
McCabe, George P. ;
Stewart-Akers, Ann M. .
TISSUE ENGINEERING PART A, 2008, 14 (11) :1835-1842
[6]   USE OF MANNOSYLATED LIPOSOMES FOR INVIVO TARGETING OF A MACROPHAGE ACTIVATOR AND CONTROL OF ARTIFICIAL PULMONARY METASTASES [J].
BARRATT, GM ;
NOLIBE, D ;
YAPO, A ;
PETIT, JF ;
TENU, JP .
ANNALES DE L INSTITUT PASTEUR-IMMUNOLOGY, 1987, 138 (03) :437-450
[7]   Macrophage specific drug delivery in experimental leishmaniasis [J].
Basu, MK ;
Lala, S .
CURRENT MOLECULAR MEDICINE, 2004, 4 (06) :681-689
[8]   Macrophage polarization in bacterial infections [J].
Benoit, Marie ;
Desnues, Benoit ;
Mege, Jean-Louis .
JOURNAL OF IMMUNOLOGY, 2008, 181 (06) :3733-3739
[9]   Macrophage phenotype as a predictor of constructive remodeling following the implantation of biologically derived surgical mesh materials [J].
Brown, Bryan N. ;
Londono, Ricardo ;
Tottey, Stephen ;
Zhang, Li ;
Kukla, Kathryn A. ;
Wolf, Matthew T. ;
Daly, Kerry A. ;
Reing, Janet E. ;
Badylak, Stephen F. .
ACTA BIOMATERIALIA, 2012, 8 (03) :978-987
[10]   CD40 ligation activates murine macrophages via an IFN-γ-dependent mechanism resulting in tumor cell destruction in vitro [J].
Buhtoiarov, IN ;
Lum, H ;
Berke, G ;
Paulnock, DM ;
Sondel, PM ;
Rakhmilevich, AL .
JOURNAL OF IMMUNOLOGY, 2005, 174 (10) :6013-6022