Control of macrophage metabolism and activation by mTOR and Akt signaling

被引:417
作者
Covarrubias, Anthony J. [1 ]
Aksoylar, H. Ibrahim [1 ]
Horng, Tiffany [1 ]
机构
[1] Harvard Univ, TH Chan Sch Publ Hlth, Dept Genet & Complex Dis, Boston, MA 02115 USA
关键词
mTOR; Akt; Macrophage activation; Macrophage metabolism; Immunometabolism; SCLEROSIS COMPLEX 1; TOLL-LIKE RECEPTORS; ALTERNATIVE ACTIVATION; MAMMALIAN TARGET; INFLAMMATORY RESPONSE; LINKS METABOLISM; PPAR-DELTA; T-CELLS; C-MYC; INNATE;
D O I
10.1016/j.smim.2015.08.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Macrophages are pleiotropic cells that assume a variety of functions depending on their tissue of residence and tissue state. They maintain homeostasis as well as coordinate responses to stresses such as infection and metabolic challenge. The ability of macrophages to acquire diverse, context-dependent activities requires their activation (or polarization) to distinct functional states. While macrophage activation is well understood at the level of signal transduction and transcriptional regulation, the metabolic underpinnings are poorly understood. Importantly, emerging studies indicate that metabolic shifts play a pivotal role in control of macrophage activation and acquisition of context-dependent effector activities. The signals that drive macrophage activation impinge on metabolic pathways, allowing for coordinate control of macrophage activation and metabolism. Here we discuss how mTOR and Akt, major metabolic regulators and targets of such activation signals, control macrophage metabolism and activation. Dys-regulated macrophage activities contribute to many diseases, including infectious, inflammatory, and metabolic diseases and cancer, thus a better understanding of metabolic control of macrophage activation could pave the way to the development of new therapeutic strategies. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:286 / 296
页数:11
相关论文
共 66 条
[1]
Disruption of Mammalian Target of Rapamycin Complex 1 in Macrophages Decreases Chemokine Gene Expression and Atherosclerosis [J].
Ai, Ding ;
Jiang, Hongfeng ;
Westerterp, Marit ;
Murphy, Andrew J. ;
Wang, Mi ;
Ganda, Anjali ;
Abramowicz, Sandra ;
Welch, Carrie ;
Almazan, Felicidad ;
Zhu, Yi ;
Miller, Yury I. ;
Tall, Alan R. .
CIRCULATION RESEARCH, 2014, 114 (10) :1576-1584
[2]
Akt1 and Akt2 protein kinases differentially contribute to macrophage polarization [J].
Arranz, Alicia ;
Doxaki, Christina ;
Vergadi, Eleni ;
de la Torre, Yeny Martinez ;
Vaporidi, Katerina ;
Lagoudaki, Eleni D. ;
Ieronymaki, Eleftheria ;
Androulidaki, Ariadne ;
Venihaki, Maria ;
Margioris, Andrew N. ;
Stathopoulos, Efstathios N. ;
Tsichlis, Philip N. ;
Tsatsanis, Christos .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (24) :9517-9522
[3]
De novo fatty acid synthesis controls the fate between regulatory T and T helper 17 cells [J].
Berod, Luciana ;
Friedrich, Christin ;
Nandan, Amrita ;
Freitag, Jenny ;
Hagemann, Stefanie ;
Harmrolfs, Kirsten ;
Sandouk, Aline ;
Hesse, Christina ;
Castro, Carla N. ;
Baehres, Heike ;
Tschirner, Sarah K. ;
Gorinski, Nataliya ;
Gohmert, Melanie ;
Mayer, Christian T. ;
Huehn, Jochen ;
Ponimaskin, Evgeni ;
Abraham, Wolf-Rainer ;
Mueller, Rolf ;
Lochner, Matthias ;
Sparwasser, Tim .
NATURE MEDICINE, 2014, 20 (11) :1327-1333
[4]
Orchestration of Metabolism by Macrophages [J].
Biswas, Subhra K. ;
Mantovani, Alberto .
CELL METABOLISM, 2012, 15 (04) :432-437
[5]
Mammalian Target of Rapamycin Complex 2 (mTORC2) Negatively Regulates Toll-like Receptor 4-mediated Inflammatory Response via FoxO1 [J].
Brown, Jonathan ;
Wang, Huizhi ;
Suttles, Jill ;
Graves, Dana T. ;
Martin, Michael .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (52) :44295-44305
[6]
The TSC-mTOR pathway regulates macrophage polarization [J].
Byles, Vanessa ;
Covarrubias, Anthony J. ;
Ben-Sahra, Issam ;
Lamming, Dudley W. ;
Sabatini, David M. ;
Manning, Brendan D. ;
Horng, Tiffany .
NATURE COMMUNICATIONS, 2013, 4
[7]
Macrophage-mediated inflammation in metabolic disease [J].
Chawla, Ajay ;
Nguyen, Khoa D. ;
Goh, Y. P. Sharon .
NATURE REVIEWS IMMUNOLOGY, 2011, 11 (11) :738-749
[8]
mTOR- and HIF-1α-mediated aerobic glycolysis as metabolic basis for trained immunity [J].
Cheng, Shih-Chin ;
Quintin, Jessica ;
Cramer, Robert A. ;
Shepardson, Kelly M. ;
Saeed, Sadia ;
Kumar, Vinod ;
Giamarellos-Bourboulis, Evangelos J. ;
Martens, Joost H. A. ;
Rao, Nagesha Appukudige ;
Aghajanirefah, Ali ;
Manjeri, Ganesh R. ;
Li, Yang ;
Ifrim, Daniela C. ;
Arts, Rob J. W. ;
van der Meer, Brian M. J. W. ;
Deen, Peter M. T. ;
Logie, Colin ;
O'Neill, Luke A. ;
Willems, Peter ;
van de Veerdonk, Frank L. ;
van der Meer, Jos W. M. ;
Ng, Aylwin ;
Joosten, Leo A. B. ;
Wijmenga, Cisca ;
Stunnenberg, Hendrik G. ;
Xavier, Ramnik J. ;
Netea, Mihai G. .
SCIENCE, 2014, 345 (6204) :1579-+
[9]
The growing landscape of lysine acetylation links metabolism and cell signalling [J].
Choudhary, Chunaram ;
Weinert, Brian T. ;
Nishida, Yuya ;
Verdin, Eric ;
Mann, Matthias .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2014, 15 (08) :536-550
[10]
Functional polarization of tumour-associated macrophages by tumour-derived lactic acid [J].
Colegio, Oscar R. ;
Ngoc-Quynh Chu ;
Szabo, Alison L. ;
Chu, Thach ;
Rhebergen, Anne Marie ;
Jairam, Vikram ;
Cyrus, Nika ;
Brokowski, Carolyn E. ;
Eisenbarth, Stephanie C. ;
Phillips, Gillian M. ;
Cline, Gary W. ;
Phillips, Andrew J. ;
Medzhitov, Ruslan .
NATURE, 2014, 513 (7519) :559-+