Modulation of IL-6 Expression by KLF4-Mediated Transactivation and PCAF-Mediated Acetylation in Sublytic C5b-9-Induced Rat Glomerular Mesangial Cells

Front Immunol. 2022 Jan 3:12:779667. doi: 10.3389/fimmu.2021.779667. eCollection 2021.

Abstract

Interleukin-6 (IL-6) overproduction has been considered to contribute to inflammatory damage of glomerular mesangial cells (GMCs) in human mesangial proliferative glomerulonephritis (MsPGN) and its rat model called Thy-1 nephritis (Thy-1N). However, the regulatory mechanisms of IL-6 expression in GMCs upon sublytic C5b-9 timulation remain poorly understood. We found that Krüppel-like factor 4 (KLF4) bound to the IL-6 promoter (-618 to -126 nt) and activated IL-6 gene transcription. Furthermore, lysine residue 224 of KLF4 was acetylated by p300/CBP-associated factor (PCAF), which was important for KLF4-mediated transactivation. Moreover, lysine residue 5 on histone H2B and lysine residue 9 on histone H3 at the IL-6 promoter were also acetylated by PCAF, which resulted in an increase in IL-6 transcription. Besides, NF-κB activation promoted IL-6 expression by elevating the expression of PCAF. Overall, these findings suggest that sublytic C5b-9-induced the expression of IL-6 involves KLF4-mediated transactivation, PCAF-mediated acetylation of KLF4 and histones, and NF-κB activation in GMCs.

Keywords: IL-6; KLF4; PCAF; acetylation; sublytic C5b-9.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Animals
  • Complement Membrane Attack Complex
  • Gene Expression Regulation / immunology*
  • Interleukin-6 / biosynthesis*
  • Kruppel-Like Factor 4 / metabolism*
  • Male
  • Mesangial Cells / metabolism*
  • Nephritis / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Transcriptional Activation
  • p300-CBP Transcription Factors / metabolism*

Substances

  • Complement Membrane Attack Complex
  • Interleukin-6
  • Kruppel-Like Factor 4
  • p300-CBP Transcription Factors
  • p300-CBP-associated factor