Metabolic programming of macrophage functions and pathogens control

被引:90
作者
Koo, Sue-jie [1 ]
Garg, Nisha J. [2 ,3 ]
机构
[1] Univ Texas Med Branch, Dept Pathol, Galveston, TX 77555 USA
[2] UTMB, Dept Microbiol & Immunol, Galveston, TX USA
[3] UTMB, Inst Human Infect & Immun, Galveston, TX USA
基金
美国国家卫生研究院;
关键词
PYRUVATE-DEHYDROGENASE KINASE; TRYPANOSOMA-CRUZI; PPAR-GAMMA; NITRIC-OXIDE; SUCCINATE-DEHYDROGENASE; ALTERNATIVE ACTIVATION; FOAM CELLS; OXIDATIVE-METABOLISM; IRON HOMEOSTASIS; APOPTOTIC CELLS;
D O I
10.1016/j.redox.2019.101198
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Macrophages (M phi) are central players in mediating proinflammatory and immunomodulatory functions. Unchecked M phi activities contribute to pathology across many diseases, including those caused by infectious pathogens and metabolic disorders. A fine balance of M phi responses is crucial, which may be achieved by enforcing appropriate bioenergetics pathways. Metabolism serves as the provider of energy, substrates, and byproducts that support differential M phi characteristics. The metabolic properties that control the polarization and response of M phi remain to be fully uncovered for use in managing infectious diseases. Here, we review the various metabolic states in M phi and how they influence the cell function.
引用
收藏
页数:12
相关论文
共 140 条
[1]   Mechanisms of phagocytosis in macrophages [J].
Aderem, A ;
Underhill, DM .
ANNUAL REVIEW OF IMMUNOLOGY, 1999, 17 :593-623
[2]   The transcriptional PPARβ/δ network in human macrophages defines a unique agonist-induced activation state [J].
Adhikary, Till ;
Wortmann, Annika ;
Schumann, Tim ;
Finkernagel, Florian ;
Lieber, Sonja ;
Roth, Katrin ;
Toth, Philipp M. ;
Diederich, Wibke E. ;
Nist, Andrea ;
Stiewe, Thorsten ;
Kleinesudeik, Lara ;
Reinartz, Silke ;
Mueller-Bruesselbach, Sabine ;
Mueller, Rolf .
NUCLEIC ACIDS RESEARCH, 2015, 43 (10) :5033-5051
[3]   Cell iron status influences macrophage polarization [J].
Agoro, Rafiou ;
Taleb, Meriem ;
Quesniaux, Valerie F. J. ;
Mura, Catherine .
PLOS ONE, 2018, 13 (05)
[4]   Toll-like receptor signalling [J].
Akira, S ;
Takeda, K .
NATURE REVIEWS IMMUNOLOGY, 2004, 4 (07) :499-511
[5]   Intracellular NAD+ levels are associated with LPS-induced TNF-α release in pro-inflammatory macrophages [J].
Al-Shabany, Abbas Jawad ;
Moody, Alan John ;
Foey, Andrew David ;
Billington, Richard Andrew .
BIOSCIENCE REPORTS, 2016, 36
[6]   Phagocytosis of apoptotic cells in homeostasis [J].
Arandjelovic, Sanja ;
Ravichandran, Kodi S. .
NATURE IMMUNOLOGY, 2015, 16 (09) :907-917
[7]   Differential effects of necrotic or apoptotic cell uptake on antigen presentation by macrophages [J].
Barker, RN ;
Erwig, LP ;
Pearce, WP ;
Devine, A ;
Rees, AJ .
PATHOBIOLOGY, 1999, 67 (5-6) :302-305
[8]   Unique Proteomic Signatures Distinguish Macrophages and Dendritic Cells [J].
Becker, Lev ;
Liu, Ning-Chun ;
Averill, Michelle M. ;
Yuan, Wei ;
Pamir, Nathalie ;
Peng, Yufeng ;
Irwin, Angela D. ;
Fu, Xiaoyun ;
Bornfeldt, Karin E. ;
Heinecke, Jay W. .
PLOS ONE, 2012, 7 (03)
[9]   HIV-Derived ssRNA Binds to TLR8 to Induce Inflammation-Driven Macrophage Foam Cell Formation [J].
Bernard, Mark A. ;
Han, Xinbing ;
Inderbitzin, Sonya ;
Agbim, Ifunanya ;
Zhao, Hui ;
Koziel, Henry ;
Tachado, Souvenir D. .
PLOS ONE, 2014, 9 (08)
[10]   Orchestration of Metabolism by Macrophages [J].
Biswas, Subhra K. ;
Mantovani, Alberto .
CELL METABOLISM, 2012, 15 (04) :432-437