Macrophage polarization in innate immune responses contributing to pathogenesis of chronic kidney disease

Abstract Chronic kidney disease (CKD) is characterized by inflammation, injury and fibrosis. Dysregulated innate immune responses mediated by macrophages play critical roles in progressive renal injury. The differentiation and polarization of macrophages into pro-inflammatory ‘M1’ and anti-inflammat...

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Main Authors: Hewang Lee, Michael B. Fessler, Peng Qu, Jurgen Heymann, Jeffrey B. Kopp
Format: Article
Language:English
Published: BMC 2020-07-01
Series:BMC Nephrology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12882-020-01921-7
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author Hewang Lee
Michael B. Fessler
Peng Qu
Jurgen Heymann
Jeffrey B. Kopp
author_facet Hewang Lee
Michael B. Fessler
Peng Qu
Jurgen Heymann
Jeffrey B. Kopp
author_sort Hewang Lee
collection DOAJ
description Abstract Chronic kidney disease (CKD) is characterized by inflammation, injury and fibrosis. Dysregulated innate immune responses mediated by macrophages play critical roles in progressive renal injury. The differentiation and polarization of macrophages into pro-inflammatory ‘M1’ and anti-inflammatory ‘M2’ states represent the two extreme maturation programs of macrophages during tissue injury. However, the effects of macrophage polarization on the pathogenesis of CKD are not fully understood. In this review, we discuss the innate immune mechanisms underlying macrophage polarization and the role of macrophage polarization in the initiation, progression, resolution and recurrence of CKD. Macrophage activation and polarization are initiated through recognition of conserved endogenous and exogenous molecular motifs by pattern recognition receptors, chiefly, Toll-like receptors (TLRs), which are located on the cell surface and in endosomes, and NLR inflammasomes, which are positioned in the cytosol. Recent data suggest that genetic variants of the innate immune molecule apolipoprotein L1 (APOL1) that are associated with increased CKD prevalence in people of African descent, mediate an atypical M1 macrophage polarization. Manipulation of macrophage polarization may offer novel strategies to address dysregulated immunometabolism and may provide a complementary approach along with current podocentric treatment for glomerular diseases.
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spelling doaj.art-9ab05c96999d43fd94e4c9ab4e32b93f2022-12-21T23:56:08ZengBMCBMC Nephrology1471-23692020-07-0121111310.1186/s12882-020-01921-7Macrophage polarization in innate immune responses contributing to pathogenesis of chronic kidney diseaseHewang Lee0Michael B. Fessler1Peng Qu2Jurgen Heymann3Jeffrey B. Kopp4Kidney Disease Section, Kidney Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of HealthImmunity, Inflammation, and Disease Laboratory, National Institute of Environmental Health Sciences, National Institutes of HealthInstitute of Heart and Vessel Diseases, Affiliated Second Hospital of Dalian Medical UniversityKidney Disease Section, Kidney Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of HealthKidney Disease Section, Kidney Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of HealthAbstract Chronic kidney disease (CKD) is characterized by inflammation, injury and fibrosis. Dysregulated innate immune responses mediated by macrophages play critical roles in progressive renal injury. The differentiation and polarization of macrophages into pro-inflammatory ‘M1’ and anti-inflammatory ‘M2’ states represent the two extreme maturation programs of macrophages during tissue injury. However, the effects of macrophage polarization on the pathogenesis of CKD are not fully understood. In this review, we discuss the innate immune mechanisms underlying macrophage polarization and the role of macrophage polarization in the initiation, progression, resolution and recurrence of CKD. Macrophage activation and polarization are initiated through recognition of conserved endogenous and exogenous molecular motifs by pattern recognition receptors, chiefly, Toll-like receptors (TLRs), which are located on the cell surface and in endosomes, and NLR inflammasomes, which are positioned in the cytosol. Recent data suggest that genetic variants of the innate immune molecule apolipoprotein L1 (APOL1) that are associated with increased CKD prevalence in people of African descent, mediate an atypical M1 macrophage polarization. Manipulation of macrophage polarization may offer novel strategies to address dysregulated immunometabolism and may provide a complementary approach along with current podocentric treatment for glomerular diseases.http://link.springer.com/article/10.1186/s12882-020-01921-7Apolipoprotein L1Chronic kidney diseaseImmunometabolismInnate immunityMacrophage polarization
spellingShingle Hewang Lee
Michael B. Fessler
Peng Qu
Jurgen Heymann
Jeffrey B. Kopp
Macrophage polarization in innate immune responses contributing to pathogenesis of chronic kidney disease
BMC Nephrology
Apolipoprotein L1
Chronic kidney disease
Immunometabolism
Innate immunity
Macrophage polarization
title Macrophage polarization in innate immune responses contributing to pathogenesis of chronic kidney disease
title_full Macrophage polarization in innate immune responses contributing to pathogenesis of chronic kidney disease
title_fullStr Macrophage polarization in innate immune responses contributing to pathogenesis of chronic kidney disease
title_full_unstemmed Macrophage polarization in innate immune responses contributing to pathogenesis of chronic kidney disease
title_short Macrophage polarization in innate immune responses contributing to pathogenesis of chronic kidney disease
title_sort macrophage polarization in innate immune responses contributing to pathogenesis of chronic kidney disease
topic Apolipoprotein L1
Chronic kidney disease
Immunometabolism
Innate immunity
Macrophage polarization
url http://link.springer.com/article/10.1186/s12882-020-01921-7
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