Contribution of endogenously produced reactive oxygen species to the activation of podocyte NLRP3 inflammasomes in hyperhomocysteinemia

Justine M. Abais, Min Xia, Guangbi Li, Todd W.B. Gehr, Krishna M. Boini, Pin Lan Li

Research output: Contribution to journalArticle

Abstract

Hyperhomocysteinemia (hHcys) is an important pathogenic factor contributing to the progression of end-stage renal disease. Recent studies have demonstrated the implication of nicotinamide adenine dinucleotide phosphate oxidase-mediated NLRP3 inflammasome activation in the development of podocyte injury and glomerular sclerosis during hHcys. However, it remains unknown which reactive oxygen species (ROS) are responsible for this activation of NLRP3 inflammasomes and how such action of ROS is controlled. This study tested the contribution of common endogenous ROS including superoxide (O2-), hydrogen peroxide (H2O2), peroxynitrite (ONOO-), and hydroxyl radical (OH) to the activation of NLRP3 inflammasomes in mouse podocytes and glomeruli. In vitro, confocal microscopy and size-exclusion chromatography demonstrated that dismutation of O2- by 4-hydroxy-2,2,6,6-tetramethylpiperidine 1-oxyl (Tempol) and decomposition of H2O2 by catalase prevented Hcys-induced aggregation of NLRP3 inflammasome proteins and inhibited Hcys-induced caspase-1 activation and IL-1β production in mouse podocytes. However, scavenging of ONOO - or OH had no significant effect on either Hcys-induced NLRP3 inflammasome formation or activation. In vivo, scavenging of O2 - by Tempol and removal of H2O2 by catalase substantially inhibited NLRP3 inflammasome formation and activation in glomeruli of hHcys mice as shown by reduced colocalization of NLRP3 with ASC or caspase-1 and inhibition of caspase-1 activation and IL-1β production. Furthermore, Tempol and catalase significantly attenuated hHcys-induced glomerular injury. In conclusion, endogenously produced O2- and H 2O2 primarily contribute to NLRP3 inflammasome formation and activation in mouse glomeruli resulting in glomerular injury or consequent sclerosis during hHcys.

Original languageEnglish (US)
Pages (from-to)211-220
Number of pages10
JournalFree Radical Biology and Medicine
Volume67
DOIs
StatePublished - Jan 1 2014
Externally publishedYes

Fingerprint

Inflammasomes
Podocytes
Hyperhomocysteinemia
Reactive Oxygen Species
Chemical activation
Caspase 1
Catalase
Sclerosis
Interleukin-1
Scavenging
Wounds and Injuries
Peroxynitrous Acid
Size exclusion chromatography
Confocal microscopy
NADP
Confocal Microscopy
Superoxides
Hydroxyl Radical
Hydrogen Peroxide
Chronic Kidney Failure

Keywords

  • Free radicals
  • Glomerular sclerosis
  • Homocysteine
  • NLRP3 inflammasome
  • Redox signaling

ASJC Scopus subject areas

  • Biochemistry
  • Physiology (medical)

Cite this

Contribution of endogenously produced reactive oxygen species to the activation of podocyte NLRP3 inflammasomes in hyperhomocysteinemia. / Abais, Justine M.; Xia, Min; Li, Guangbi; Gehr, Todd W.B.; Boini, Krishna M.; Li, Pin Lan.

In: Free Radical Biology and Medicine, Vol. 67, 01.01.2014, p. 211-220.

Research output: Contribution to journalArticle

Abais, Justine M. ; Xia, Min ; Li, Guangbi ; Gehr, Todd W.B. ; Boini, Krishna M. ; Li, Pin Lan. / Contribution of endogenously produced reactive oxygen species to the activation of podocyte NLRP3 inflammasomes in hyperhomocysteinemia. In: Free Radical Biology and Medicine. 2014 ; Vol. 67. pp. 211-220.
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AB - Hyperhomocysteinemia (hHcys) is an important pathogenic factor contributing to the progression of end-stage renal disease. Recent studies have demonstrated the implication of nicotinamide adenine dinucleotide phosphate oxidase-mediated NLRP3 inflammasome activation in the development of podocyte injury and glomerular sclerosis during hHcys. However, it remains unknown which reactive oxygen species (ROS) are responsible for this activation of NLRP3 inflammasomes and how such action of ROS is controlled. This study tested the contribution of common endogenous ROS including superoxide (O2-), hydrogen peroxide (H2O2), peroxynitrite (ONOO-), and hydroxyl radical (OH) to the activation of NLRP3 inflammasomes in mouse podocytes and glomeruli. In vitro, confocal microscopy and size-exclusion chromatography demonstrated that dismutation of O2- by 4-hydroxy-2,2,6,6-tetramethylpiperidine 1-oxyl (Tempol) and decomposition of H2O2 by catalase prevented Hcys-induced aggregation of NLRP3 inflammasome proteins and inhibited Hcys-induced caspase-1 activation and IL-1β production in mouse podocytes. However, scavenging of ONOO - or OH had no significant effect on either Hcys-induced NLRP3 inflammasome formation or activation. In vivo, scavenging of O2 - by Tempol and removal of H2O2 by catalase substantially inhibited NLRP3 inflammasome formation and activation in glomeruli of hHcys mice as shown by reduced colocalization of NLRP3 with ASC or caspase-1 and inhibition of caspase-1 activation and IL-1β production. Furthermore, Tempol and catalase significantly attenuated hHcys-induced glomerular injury. In conclusion, endogenously produced O2- and H 2O2 primarily contribute to NLRP3 inflammasome formation and activation in mouse glomeruli resulting in glomerular injury or consequent sclerosis during hHcys.

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