Systematic validation of specific phenotypic markers for in vitro polarized human macrophages

被引:346
作者
Ambarus, C. A. [1 ]
Krausz, S. [1 ]
van Eijk, M.
Hamann, J. [2 ]
Radstake, T. R. D. J. [3 ,4 ]
Reedquist, K. A. [1 ,2 ]
Tak, P. P. [1 ]
Baeten, D. L. P. [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Clin Immunol & Rheumatol, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Med Biochem, NL-1105 AZ Amsterdam, Netherlands
[3] Nijmegen Inst Infect Inflammat & Immun, Nijmegen, Netherlands
[4] Radboud Univ Nijmegen, Med Ctr, Dept Rheumatol, Nijmegen, Netherlands
关键词
Macrophage polarization; Cell surface molecules; Phenotypic markers; Flow cytometry; Inflammation; TUMOR-ASSOCIATED MACROPHAGES; ADIPOSE-TISSUE MACROPHAGES; SCAVENGER RECEPTOR CD163; ALTERNATIVE ACTIVATION; TYPE-2; MACROPHAGES; MONOCYTE; DIFFERENTIATION; ANTIGEN; CELLS; IDENTIFICATION;
D O I
10.1016/j.jim.2011.10.013
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Background: Polarization of macrophages by specific micro-environmental conditions impacts upon their function following subsequent activation. This study aimed to systematically validate robust phenotypic markers for in vitro polarized human macrophages in order to facilitate the study of macrophage subsets in vivo. Methods: Human peripheral blood monocytes were polarized in vitro with IFN-gamma, IL-4, or IL-10. Similar experiments were performed with TNF. IL-13, dexamethasone, M-CSF and GM-CSF as polarizing stimuli. Phenotypic markers were assessed by flow cytometry and qPCR. Results: IFN-gamma polarized macrophages (M Phi(IFN-gamma)) specifically enhanced membrane expression of CD80 and CD64, IL-4 polarized macrophages (M Phi(IL-4)) mainly upregulated CD200R and CD206, and downregulated CD14 levels, and IL-10 polarized macrophages (M Phi(IL-10)) selectively induced CD163, CD16, and CD32. The expression profiles of the most specific markers were confirmed by qPCR, dose-response experiments, and the use of alternative polarizing factors for each macrophage subset (TNF, IL-13, and dexamethasone, respectively). GM-CSF polarized macrophages (M Phi(GM-CSF)) upregulated CD80 but not CD64 expression, showing a partial phenotypic similarity with M Phi(IFN-gamma), and also upregulated the expression of the alternative activation marker CD206. M-CSF polarized macrophages (M Phi(M-CSF)) not only expressed increased levels of CD163 and CD16, resembling M Phi(IL-10), but also displayed high levels of CD64. The phenotype of M Phi(M-CSF) could be further modulated by additional polarization with IFN-gamma, IL-4, or IL-10, whereas M Phi(GM-CSF) showed less phenotypic plasticity. Conclusion: This study validated CD80 as the most robust phenotypic marker for human M Phi(IL-gamma), whereas CD200R was upregulated and CD14 was specifically downregulated on M Phi(IL-4) CD163 and CD16 were found to be specific markers for M Phi(IL-10). The GM-CSF/M-CSF differentiation model showed only a partial phenotypic similarity with the IFN-gamma/IL-4/IL-10 induced polarization. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:196 / 206
页数:11
相关论文
共 56 条
[1]
Anderson CF, 2002, J LEUKOCYTE BIOL, V72, P101
[2]
Cutting edge:: Biasing immune responses by directing antigen to macrophage Fcγ receptors [J].
Anderson, CF ;
Mosser, DM .
JOURNAL OF IMMUNOLOGY, 2002, 168 (08) :3697-3701
[3]
Macrophages expressing the scavenger receptor CD163: a link between immune alterations of the gut and synovial inflammation in spondyloarthropathy [J].
Baeten, D ;
Demetter, P ;
Cuvelier, CA ;
Kruithof, E ;
Van Damme, N ;
De Vos, M ;
Veys, EM ;
De Keyser, F .
JOURNAL OF PATHOLOGY, 2002, 196 (03) :343-350
[4]
Association of CD163+ macrophages and local production of soluble CD163 with decreased lymphocyte activation in spondylarthropathy synovitis [J].
Baeten, D ;
Moller, HJ ;
Delanghe, J ;
Veys, EM ;
Moestrup, SK ;
De Keyser, F .
ARTHRITIS AND RHEUMATISM, 2004, 50 (05) :1611-1623
[5]
Plasticity of macrophage function during tumor progression: Regulation by distinct molecular mechanisms [J].
Biswas, Subhra K. ;
Sica, Antonio ;
Lewis, Claire E. .
JOURNAL OF IMMUNOLOGY, 2008, 180 (04) :2011-2017
[6]
Increased expression of Fcγ receptors II and III on macrophages of rheumatoid arthritis patients results in higher production of tumor necrosis factor α and matrix metalloproteinase [J].
Blom, AB ;
Radstake, TRDJ ;
Holthuysen, AEM ;
Slöetjes, AW ;
Pesman, GJ ;
Sweep, FGJ ;
van de Loo, FAJ ;
Joosten, LAB ;
Barrera, P ;
van Lent, PLEM ;
van den Berg, WB .
ARTHRITIS AND RHEUMATISM, 2003, 48 (04) :1002-1014
[7]
MACROPHAGE DEACTIVATION BY INTERLEUKIN-10 [J].
BOGDAN, C ;
VODOVOTZ, Y ;
NATHAN, C .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 174 (06) :1549-1555
[8]
Tumor-associated macrophages: The double-edged sword in cancer progression [J].
Chen, JJW ;
Lin, YC ;
Yao, PL ;
Yuan, A ;
Chen, HY ;
Shun, CT ;
Tsai, MF ;
Chen, CH ;
Yang, PC .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (05) :953-964
[9]
Differential regulation of the mannose and SP-A receptors on macrophages [J].
Chroneos, Z ;
Shepherd, VL .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1995, 269 (06) :L721-L726
[10]
Monoclonal anti body-mediated CD200 receptor signaling suppresses macrophage activation and tissue damage in experimental autoimmune uveoretinitis [J].
Copland, David A. ;
Calder, Claudia J. ;
Raveney, Ben J. E. ;
Nicholson, Lindsay B. ;
Phillips, Joseph ;
Cherwinski, Holly ;
Jenmalm, Maria ;
Sedgwick, Jonathon D. ;
Dick, Andrew D. .
AMERICAN JOURNAL OF PATHOLOGY, 2007, 171 (02) :580-588