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Diverse Roles of Mitochondria in Immune Responses: Novel Insights Into Immuno-Metabolism

Lack of immune system cells or impairment in differentiation of immune cells is the basis for many chronic diseases. Metabolic changes could be the root cause for this immune cell impairment. These changes could be a result of altered transcription, cytokine production from surrounding cells, and ch...

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Autores principales: Angajala, Anusha, Lim, Sangbin, Phillips, Joshua B., Kim, Jin-Hwan, Yates, Clayton, You, Zongbing, Tan, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6052888/
https://www.ncbi.nlm.nih.gov/pubmed/30050539
http://dx.doi.org/10.3389/fimmu.2018.01605
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author Angajala, Anusha
Lim, Sangbin
Phillips, Joshua B.
Kim, Jin-Hwan
Yates, Clayton
You, Zongbing
Tan, Ming
author_facet Angajala, Anusha
Lim, Sangbin
Phillips, Joshua B.
Kim, Jin-Hwan
Yates, Clayton
You, Zongbing
Tan, Ming
author_sort Angajala, Anusha
collection PubMed
description Lack of immune system cells or impairment in differentiation of immune cells is the basis for many chronic diseases. Metabolic changes could be the root cause for this immune cell impairment. These changes could be a result of altered transcription, cytokine production from surrounding cells, and changes in metabolic pathways. Immunity and mitochondria are interlinked with each other. An important feature of mitochondria is it can regulate activation, differentiation, and survival of immune cells. In addition, it can also release signals such as mitochondrial DNA (mtDNA) and mitochondrial ROS (mtROS) to regulate transcription of immune cells. From current literature, we found that mitochondria can regulate immunity in different ways. First, alterations in metabolic pathways (TCA cycle, oxidative phosphorylation, and FAO) and mitochondria induced transcriptional changes can lead to entirely different outcomes in immune cells. For example, M1 macrophages exhibit a broken TCA cycle and have a pro-inflammatory role. By contrast, M2 macrophages undergo β-oxidation to produce anti-inflammatory responses. In addition, amino acid metabolism, especially arginine, glutamine, serine, glycine, and tryptophan, is critical for T cell differentiation and macrophage polarization. Second, mitochondria can activate the inflammatory response. For instance, mitochondrial antiviral signaling and NLRP3 can be activated by mitochondria. Third, mitochondrial mass and mobility can be influenced by fission and fusion. Fission and fusion can influence immune functions. Finally, mitochondria are placed near the endoplasmic reticulum (ER) in immune cells. Therefore, mitochondria and ER junction signaling can also influence immune cell metabolism. Mitochondrial machinery such as metabolic pathways, amino acid metabolism, antioxidant systems, mitochondrial dynamics, mtDNA, mitophagy, and mtROS are crucial for immune functions. Here, we have demonstrated how mitochondria coordinate to alter immune responses and how changes in mitochondrial machinery contribute to alterations in immune responses. A better understanding of the molecular components of mitochondria is necessary. This can help in the development of safe and effective immune therapy or prevention of chronic diseases. In this review, we have presented an updated prospective of the mitochondrial machinery that drives various immune responses.
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spelling pubmed-60528882018-07-26 Diverse Roles of Mitochondria in Immune Responses: Novel Insights Into Immuno-Metabolism Angajala, Anusha Lim, Sangbin Phillips, Joshua B. Kim, Jin-Hwan Yates, Clayton You, Zongbing Tan, Ming Front Immunol Immunology Lack of immune system cells or impairment in differentiation of immune cells is the basis for many chronic diseases. Metabolic changes could be the root cause for this immune cell impairment. These changes could be a result of altered transcription, cytokine production from surrounding cells, and changes in metabolic pathways. Immunity and mitochondria are interlinked with each other. An important feature of mitochondria is it can regulate activation, differentiation, and survival of immune cells. In addition, it can also release signals such as mitochondrial DNA (mtDNA) and mitochondrial ROS (mtROS) to regulate transcription of immune cells. From current literature, we found that mitochondria can regulate immunity in different ways. First, alterations in metabolic pathways (TCA cycle, oxidative phosphorylation, and FAO) and mitochondria induced transcriptional changes can lead to entirely different outcomes in immune cells. For example, M1 macrophages exhibit a broken TCA cycle and have a pro-inflammatory role. By contrast, M2 macrophages undergo β-oxidation to produce anti-inflammatory responses. In addition, amino acid metabolism, especially arginine, glutamine, serine, glycine, and tryptophan, is critical for T cell differentiation and macrophage polarization. Second, mitochondria can activate the inflammatory response. For instance, mitochondrial antiviral signaling and NLRP3 can be activated by mitochondria. Third, mitochondrial mass and mobility can be influenced by fission and fusion. Fission and fusion can influence immune functions. Finally, mitochondria are placed near the endoplasmic reticulum (ER) in immune cells. Therefore, mitochondria and ER junction signaling can also influence immune cell metabolism. Mitochondrial machinery such as metabolic pathways, amino acid metabolism, antioxidant systems, mitochondrial dynamics, mtDNA, mitophagy, and mtROS are crucial for immune functions. Here, we have demonstrated how mitochondria coordinate to alter immune responses and how changes in mitochondrial machinery contribute to alterations in immune responses. A better understanding of the molecular components of mitochondria is necessary. This can help in the development of safe and effective immune therapy or prevention of chronic diseases. In this review, we have presented an updated prospective of the mitochondrial machinery that drives various immune responses. Frontiers Media S.A. 2018-07-12 /pmc/articles/PMC6052888/ /pubmed/30050539 http://dx.doi.org/10.3389/fimmu.2018.01605 Text en Copyright © 2018 Angajala, Lim, Phillips, Kim, Yates, You and Tan. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Angajala, Anusha
Lim, Sangbin
Phillips, Joshua B.
Kim, Jin-Hwan
Yates, Clayton
You, Zongbing
Tan, Ming
Diverse Roles of Mitochondria in Immune Responses: Novel Insights Into Immuno-Metabolism
title Diverse Roles of Mitochondria in Immune Responses: Novel Insights Into Immuno-Metabolism
title_full Diverse Roles of Mitochondria in Immune Responses: Novel Insights Into Immuno-Metabolism
title_fullStr Diverse Roles of Mitochondria in Immune Responses: Novel Insights Into Immuno-Metabolism
title_full_unstemmed Diverse Roles of Mitochondria in Immune Responses: Novel Insights Into Immuno-Metabolism
title_short Diverse Roles of Mitochondria in Immune Responses: Novel Insights Into Immuno-Metabolism
title_sort diverse roles of mitochondria in immune responses: novel insights into immuno-metabolism
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6052888/
https://www.ncbi.nlm.nih.gov/pubmed/30050539
http://dx.doi.org/10.3389/fimmu.2018.01605
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