Sirtuins Link Inflammation and Metabolism

Sirtuins (SIRT), first discovered in yeast as NAD+ dependent epigenetic and metabolic regulators, have comparable activities in human physiology and disease. Mounting evidence supports that the seven-member mammalian sirtuin family (SIRT1–7) guard homeostasis by sensing bioenergy needs and respondin...

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Main Authors: Vidula T. Vachharajani, Tiefu Liu, Xianfeng Wang, Jason J. Hoth, Barbara K. Yoza, Charles E. McCall
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:Journal of Immunology Research
Online Access:http://dx.doi.org/10.1155/2016/8167273
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author Vidula T. Vachharajani
Tiefu Liu
Xianfeng Wang
Jason J. Hoth
Barbara K. Yoza
Charles E. McCall
author_facet Vidula T. Vachharajani
Tiefu Liu
Xianfeng Wang
Jason J. Hoth
Barbara K. Yoza
Charles E. McCall
author_sort Vidula T. Vachharajani
collection DOAJ
description Sirtuins (SIRT), first discovered in yeast as NAD+ dependent epigenetic and metabolic regulators, have comparable activities in human physiology and disease. Mounting evidence supports that the seven-member mammalian sirtuin family (SIRT1–7) guard homeostasis by sensing bioenergy needs and responding by making alterations in the cell nutrients. Sirtuins play a critical role in restoring homeostasis during stress responses. Inflammation is designed to “defend and mend” against the invading organisms. Emerging evidence supports that metabolism and bioenergy reprogramming direct the sequential course of inflammation; failure of homeostasis retrieval results in many chronic and acute inflammatory diseases. Anabolic glycolysis quickly induced (compared to oxidative phosphorylation) for ROS and ATP generation is needed for immune activation to “defend” against invading microorganisms. Lipolysis/fatty acid oxidation, essential for cellular protection/hibernation and cell survival in order to “mend,” leads to immune repression. Acute/chronic inflammations are linked to altered glycolysis and fatty acid oxidation, at least in part, by NAD+ dependent function of sirtuins. Therapeutically targeting sirtuins may provide a new class of inflammation and immune regulators. This review discusses how sirtuins integrate metabolism, bioenergetics, and immunity during inflammation and how sirtuin-directed treatment improves outcome in chronic inflammatory diseases and in the extreme stress response of sepsis.
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spelling doaj-art-e353b1d0c09a425495ca2a60fd53a62e2025-08-20T03:26:30ZengWileyJournal of Immunology Research2314-88612314-71562016-01-01201610.1155/2016/81672738167273Sirtuins Link Inflammation and MetabolismVidula T. Vachharajani0Tiefu Liu1Xianfeng Wang2Jason J. Hoth3Barbara K. Yoza4Charles E. McCall5Department of Anesthesiology, Wake Forest School of Medicine, Winston-Salem, NC 27157, USADepartment of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC 27157, USADepartment of Anesthesiology, Wake Forest School of Medicine, Winston-Salem, NC 27157, USADepartment of Surgery, Wake Forest School of Medicine, Winston-Salem, NC 27157, USADepartment of Surgery, Wake Forest School of Medicine, Winston-Salem, NC 27157, USADepartment of Anesthesiology, Wake Forest School of Medicine, Winston-Salem, NC 27157, USASirtuins (SIRT), first discovered in yeast as NAD+ dependent epigenetic and metabolic regulators, have comparable activities in human physiology and disease. Mounting evidence supports that the seven-member mammalian sirtuin family (SIRT1–7) guard homeostasis by sensing bioenergy needs and responding by making alterations in the cell nutrients. Sirtuins play a critical role in restoring homeostasis during stress responses. Inflammation is designed to “defend and mend” against the invading organisms. Emerging evidence supports that metabolism and bioenergy reprogramming direct the sequential course of inflammation; failure of homeostasis retrieval results in many chronic and acute inflammatory diseases. Anabolic glycolysis quickly induced (compared to oxidative phosphorylation) for ROS and ATP generation is needed for immune activation to “defend” against invading microorganisms. Lipolysis/fatty acid oxidation, essential for cellular protection/hibernation and cell survival in order to “mend,” leads to immune repression. Acute/chronic inflammations are linked to altered glycolysis and fatty acid oxidation, at least in part, by NAD+ dependent function of sirtuins. Therapeutically targeting sirtuins may provide a new class of inflammation and immune regulators. This review discusses how sirtuins integrate metabolism, bioenergetics, and immunity during inflammation and how sirtuin-directed treatment improves outcome in chronic inflammatory diseases and in the extreme stress response of sepsis.http://dx.doi.org/10.1155/2016/8167273
spellingShingle Vidula T. Vachharajani
Tiefu Liu
Xianfeng Wang
Jason J. Hoth
Barbara K. Yoza
Charles E. McCall
Sirtuins Link Inflammation and Metabolism
Journal of Immunology Research
title Sirtuins Link Inflammation and Metabolism
title_full Sirtuins Link Inflammation and Metabolism
title_fullStr Sirtuins Link Inflammation and Metabolism
title_full_unstemmed Sirtuins Link Inflammation and Metabolism
title_short Sirtuins Link Inflammation and Metabolism
title_sort sirtuins link inflammation and metabolism
url http://dx.doi.org/10.1155/2016/8167273
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AT tiefuliu sirtuinslinkinflammationandmetabolism
AT xianfengwang sirtuinslinkinflammationandmetabolism
AT jasonjhoth sirtuinslinkinflammationandmetabolism
AT barbarakyoza sirtuinslinkinflammationandmetabolism
AT charlesemccall sirtuinslinkinflammationandmetabolism