Involvement of NF-κBIZ and related cytokines in age-associated renal fibrosis

Oncotarget. 2017 Jan 31;8(5):7315-7327. doi: 10.18632/oncotarget.14614.

Abstract

Chronic inflammation is a major contributor to age-related nephropathic changes, including renal fibrosis. In this study, various experimental paradigms were designed to delineate the role played by NF-κBIZ (also known as IκBζ) in age-associated renal fibrosis. Analyses based on RNA-sequencing findings obtained by next generation sequencing (NGS) revealed the upregulations of NF-κBIZ and of IL-6 and MCP-1 (both known to be regulated by NF-κBIZ) during aging. The up-regulation of NF-κBIZ in aged rat kidneys coincided with increased macrophage infiltration. In LPS-treated macrophages, oxidative stress was found to play a pivotal role in NF-κBIZ expression, suggesting age-related oxidative stress is associated with NF-κBIZ activation. Furthermore, these in vitro findings were confirmed in LPS-treated old rats, which showed higher levels of oxidative stress and NF-κBIZ in kidneys than LPS-treated young rats. Additional in vitro experiments using macrophages and kidney fibroblasts demonstrated NF-κBIZ and related cytokines participate in fibrosis. In particular, increased levels of NF-κBIZ-associated cytokines in macrophages significantly up-regulated TGF-β induced kidney fibroblast activation. Moreover, experiments with NF-κBIZ knocked down macrophages showed reduced TGF-β-induced kidney fibroblast activation. The findings of the present study provide evidence regarding an involvement of NF-κBIZ in age-associated progressive renal fibrosis and provides potential targets for its prevention.

Keywords: NF-κBIZ; aging; inflammation; renal fibrosis.

Publication types

  • Comparative Study

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / metabolism
  • Age Factors
  • Aging / genetics
  • Aging / metabolism*
  • Aging / pathology
  • Animals
  • Cells, Cultured
  • Chemokine CCL2 / metabolism
  • Cytokines / metabolism*
  • Disease Models, Animal
  • Fibroblasts / metabolism
  • Fibroblasts / pathology
  • Fibrosis
  • I-kappa B Proteins / metabolism*
  • Interleukin-6 / metabolism
  • Kidney / metabolism*
  • Kidney / pathology
  • Kidney Diseases / chemically induced
  • Kidney Diseases / genetics
  • Kidney Diseases / metabolism*
  • Kidney Diseases / pathology
  • Lipopolysaccharides
  • Macrophages, Peritoneal / metabolism
  • Macrophages, Peritoneal / pathology
  • Male
  • Mice, Inbred C57BL
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • Oxidative Stress
  • Rats, Sprague-Dawley
  • Signal Transduction
  • Time Factors
  • Transfection

Substances

  • Adaptor Proteins, Signal Transducing
  • Ccl2 protein, rat
  • Chemokine CCL2
  • Cytokines
  • I-kappa B Proteins
  • Interleukin-6
  • Lipopolysaccharides
  • NFKBIZ protein, rat
  • Nfkbiz protein, mouse
  • Nuclear Proteins
  • lipopolysaccharide, E coli O55-B5