In 1986 and 1987, Philip Newsholme et al. reported macrophages utilize glutamine, as well as glucose, at high rates. These authors measured key enzyme activities and consumption and production levels of metabolites in incubated or cultured macrophages isolated from the mouse or rat intraperitoneal cavity. Metabolic pathways essential for macrophage function were then determined. Macrophages utilize glucose to generate (i) ATP in the pathways of glycolysis and mitochondrial oxidative phosphorylation, (ii) glycerol 3-phosphate for the synthesis of phospholipids and triacylglycerols, (iii) NADPH for the production of reactive oxygen species (ROS) and (iv) ribose for the synthesis of RNA and subsequently production and secretion of protein mediators (e.g. cytokines). Glutamine plays an essential role in macrophage metabolism and function, as it is required for energy production but also provides nitrogen for synthesis of purines, pyrimidines and thus RNA. Macrophages also utilize fatty acids for both energy production in the mitochondria and lipid synthesis essential to plasma membrane turnover and lipid meditator production. Recent studies utilizing metabolomic approaches, transcriptional and metabolite tracking technologies have detailed mitochondrial release of tricarboxylic acid (TCA) intermediates (e.g. citrate and succinate) to the cytosol, which then regulate pro-inflammatory responses. Macrophages can reprogramme their metabolism and function according to environmental conditions and stimuli in order to polarize phenotype so generating pro- or anti-inflammatory cells. Changes in macrophage metabolism result in modified function/phenotype and vice versa. The plasticity of macrophage metabolism allows the cell to quickly respond to changes in environmental conditions such as those induced by hormones and/or inflammation. A past and present overview of macrophage metabolism and impact of endocrine regulation and the relevance to human disease are described in this review.
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June 2017
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The accompanying caption is: Image demonstrates a 3D reconstruction of the neurovascular unit in a hippocampal artery in the mouse brain. For further details, see article by Nizari et al in this issue, pages 1207-1214. Image kindly provided by Cheryl Hawkes.Close Modal
Review Article|
June 07 2017
A past and present overview of macrophage metabolism and functional outcomes
Rui Curi;
Rui Curi
*
1Department of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, Av. Prof. Lineu Prestes, 1524, SP 05508-900, Brazil
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Renata de Siqueira Mendes;
Renata de Siqueira Mendes
*
1Department of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, Av. Prof. Lineu Prestes, 1524, SP 05508-900, Brazil
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Luiz Aurélio de Campos Crispin;
Luiz Aurélio de Campos Crispin
2Laboratory of Pathophysiology, Butantan Institute, Av. Vital Brazil, 1500, SP 05503-900, São Paulo, Brazil
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Giuseppe Danilo Norata;
Giuseppe Danilo Norata
3School of Biomedical Sciences, Curtin Health Innovation Research Institute (CHIRI), Curtin University, Perth, WA, Australia
4Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Milan, Italy
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Sandra Coccuzzo Sampaio;
Sandra Coccuzzo Sampaio
2Laboratory of Pathophysiology, Butantan Institute, Av. Vital Brazil, 1500, SP 05503-900, São Paulo, Brazil
5Department of Pharmacology, Institute of Biomedical Sciences, University of São Paulo, Av. Prof. Lineu Prestes, 1524, SP 05508-900, Brazil
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Philip Newsholme
3School of Biomedical Sciences, Curtin Health Innovation Research Institute (CHIRI), Curtin University, Perth, WA, Australia
Correspondence: Philip Newsholme (Philip.Newsholme@curtin.edu.au)
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Clin Sci (Lond) (2017) 131 (12): 1329–1342.
Article history
Received:
March 16 2017
Revision Received:
March 16 2017
Accepted:
March 22 2017
Citation
Rui Curi, Renata de Siqueira Mendes, Luiz Aurélio de Campos Crispin, Giuseppe Danilo Norata, Sandra Coccuzzo Sampaio, Philip Newsholme; A past and present overview of macrophage metabolism and functional outcomes. Clin Sci (Lond) 1 June 2017; 131 (12): 1329–1342. doi: https://doi.org/10.1042/CS20170220
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