Macrophage activation and polarization

被引:2440
作者
Martinez, Fernando Oneissi [1 ]
Sica, Antonio [1 ]
Mantovani, Alberto [1 ,2 ]
Locati, Massimo [1 ,2 ]
机构
[1] Ist Clin Humanitas, I-20089 Rozzano, Italy
[2] Univ Milan, Inst Gen Pathol, I-20133 Milan, Italy
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2008年 / 13卷
关键词
macrophage; activation; polarization; LPS; interferon gamma; IL-4; IL-10; IL-13; immune complexes; glucocorticoids; review;
D O I
10.2741/2692
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Macrophages are widely distributed immune system cells that play an indispensable role in homeostasis and defense. They can be phenotypically polarized by the microenvironment to mount specific functional programs. Polarized macrophages can be broadly classified in two main groups: classically activated macrophages (or M1), whose prototypical activating stimuli are IFNgamma and LPS, and alternatively activated macrophages (or M2), further subdivided in M2a (after exposure to IL-4 or IL-13), M2b (immune complexes in combination with IL-1beta or LPS) and M2c (IL-10, TGFbeta or glucocorticoids). M1 exhibit potent microbicidal properties and promote strong IL-12-mediated Th1 responses, whilst M2 support Th2-associated effector functions. Beyond infection M2 polarized macrophages play a role in resolution of inflammation through high endocityc clearance capacities and trophic factor synthesis, accompanied by reduced pro-inflammatory cytokine secretion. Similar functions are also exerted by tumor-associated macrophages (TAM), which also display an alternative-like activation phenotype and play a detrimental pro-tumoral role. Here we review the main functions of polarized macrophages and discuss the perpectives of this field.
引用
收藏
页码:453 / 461
页数:9
相关论文
共 79 条
[1]
Adams D O, 1989, Year Immunol, V4, P159
[2]
MOLECULAR-INTERACTIONS IN MACROPHAGE ACTIVATION [J].
ADAMS, DO .
IMMUNOLOGY TODAY, 1989, 10 (02) :33-35
[3]
Involvement of caspase-1 and caspase-3 in the production and processing of mature human interleukin 18 in monocytic THP.1 cells [J].
Akita, K ;
Ohtsuki, T ;
Nukada, Y ;
Tanimoto, T ;
Namba, M ;
Okura, T ;
TakakuraYamamoto, R ;
Torigoe, K ;
Gu, Y ;
Su, MSS ;
Fujii, M ;
SatohItoh, M ;
Yamamoto, K ;
Kohno, K ;
Ikeda, M ;
Kurimoto, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (42) :26595-26603
[4]
The chemokine receptor switch paradigm and dendritic cell migration: its significance in tumor tissues [J].
Allavena, P ;
Sica, A ;
Vecchi, A ;
Locati, M ;
Sozzani, S ;
Mantovani, A .
IMMUNOLOGICAL REVIEWS, 2000, 177 :141-149
[5]
Anderson CF, 2002, J LEUKOCYTE BIOL, V72, P101
[6]
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
[7]
A distinct and unique transcriptional program expressed by tumor-associated macrophages (defective NF-κB and enhanced IRF-3/STAT1 activation) [J].
Biswas, SK ;
Gangi, L ;
Paul, S ;
Schioppa, T ;
Saccani, A ;
Sironi, M ;
Bottazzi, B ;
Doni, A ;
Vincenzo, B ;
Pasqualini, F ;
Vago, L ;
Nebuloni, M ;
Mantovani, A ;
Sica, A .
BLOOD, 2006, 107 (05) :2112-2122
[8]
Cellular responses to interferon-gamma [J].
Boehm, U ;
Klamp, T ;
Groot, M ;
Howard, JC .
ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 :749-795
[9]
BOGDAN C, 1992, J BIOL CHEM, V267, P23301
[10]
The interleukin-1 receptor/Toll-like receptor superfamily: signal generators for pro-inflammatory interleukins and microbial products [J].
Bowie, A ;
O'Neill, LAJ .
JOURNAL OF LEUKOCYTE BIOLOGY, 2000, 67 (04) :508-514