Macrophage Polarization in Health and Disease

被引:240
作者
Cassetta, Luca [3 ]
Cassol, Edana [4 ]
Poli, Guido [1 ,2 ]
机构
[1] Ist Sci San Raffaele, AIDS Immunopathogenesis Unit, Div Immunol Transplantat & Infect Dis, Sch Med, I-20132 Milan, Italy
[2] Univ Vita Salute San Raffaele, Labs P2 P3, I-20132 Milan, Italy
[3] Albert Einstein Coll Med, Dept Dev & Mol Biol, Ctr Study Reprod Biol & Womens Hlth, Bronx, NY 10461 USA
[4] Dana Farber Canc Inst, Dept Canc Immunol & AIDS, Boston, MA 02115 USA
来源
THESCIENTIFICWORLDJOURNAL | 2011年 / 11卷
关键词
Macrophage; polarization; M1/M2; HIV; tumors; TAMs (tumor-associated macrophages); regulatory macrophages; TUMOR-ASSOCIATED MACROPHAGES; REGULATORY T-CELLS; NF-KAPPA-B; ALTERNATIVE ACTIVATION; MONOCYTE FUNCTION; SUPPRESSOR-CELLS; MAMMARY-TUMORS; STAPHYLOCOCCUS-AUREUS; HELMINTH INFECTION; MONONUCLEAR-CELLS;
D O I
10.1100/2011/213962
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Macrophages are terminally differentiated cells of the mononuclear phagocyte system that also encompasses dendritic cells, circulating blood monocytes, and committed myeloid progenitor cells in the bone marrow. Both macrophages and their monocytic precursors can change their functional state in response to microenvironmental cues exhibiting a marked heterogeneity. However, there are still uncertainties regarding distinct expression patterns of surface markers that clearly define macrophage subsets, particularly in the case of human macrophages. In addition to their tissue distribution, macrophages can be functionally polarized into M1 (proinflammatory) and M2 (alternatively activated) as well as regulatory cells in response to both exogenous infections and solid tumors as well as by systems biology approaches.
引用
收藏
页码:2391 / 2402
页数:12
相关论文
共 80 条
[1]   DCs and NK cells: critical effectors in the immune response to HIV-1 [J].
Altfeld, Marcus ;
Fadda, Lena ;
Frleta, Davor ;
Bhardwaj, Nina .
NATURE REVIEWS IMMUNOLOGY, 2011, 11 (03) :176-186
[2]   Smoldering and polarized inflammation in the initiation and promotion of malignant disease [J].
Balkwill, F ;
Charles, KA ;
Mantovani, A .
CANCER CELL, 2005, 7 (03) :211-217
[3]   APOBEC3A Is a Specific Inhibitor of the Early Phases of HIV-1 Infection in Myeloid Cells [J].
Berger, Gregory ;
Durand, Stephanie ;
Fargier, Guillaume ;
Xuan-Nhi Nguyen ;
Cordeil, Stepanie ;
Bouaziz, Serge ;
Muriaux, Delphine ;
Darlix, Jean-Luc ;
Cimarelli, Andrea .
PLOS PATHOGENS, 2011, 7 (09)
[4]   The role of tumour-associated macrophages in tumour progression: implications for new anticancer therapies [J].
Bingle, L ;
Brown, NJ ;
Lewis, CE .
JOURNAL OF PATHOLOGY, 2002, 196 (03) :254-265
[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]   HIV-1 Activates Macrophages Independent of Toll-Like Receptors [J].
Brown, Joseph N. ;
Kohler, James J. ;
Coberley, Carter R. ;
Sleasman, John W. ;
Goodenow, Maureen M. .
PLOS ONE, 2008, 3 (12)
[7]   Cell Biology of HIV-1 Infection of Macrophages [J].
Carter, Carol A. ;
Ehrlich, Lorna S. .
ANNUAL REVIEW OF MICROBIOLOGY, 2008, 62 :425-443
[8]   M1 and M2a Polarization of Human Monocyte-Derived Macrophages Inhibits HIV-1 Replication by Distinct Mechanisms [J].
Cassol, Edana ;
Cassetta, Luca ;
Rizzi, Chiara ;
Alfano, Massimo ;
Poli, Guido .
JOURNAL OF IMMUNOLOGY, 2009, 182 (10) :6237-6246
[9]   Macrophages: Obligate partners for tumor cell migration, invasion, and metastasis [J].
Condeelis, J ;
Pollard, JW .
CELL, 2006, 124 (02) :263-266
[10]   Inflammation and cancer [J].
Coussens, LM ;
Werb, Z .
NATURE, 2002, 420 (6917) :860-867