Epigenetics and expression of key genes associated with cardiac fibrosis: NLRP3, MMP2, MMP9, CCN2/CTGF and AGT

Epigenomics. 2021 Feb;13(3):219-234. doi: 10.2217/epi-2020-0446. Epub 2021 Feb 4.

Abstract

Aims: Excessive inflammatory signaling and pathological remodeling of the extracellular matrix drive cardiac fibrosis and require changes in gene expression. Materials and methods: Using bioinformatics, both tissue-specific expression profiles and epigenomic profiles of some genes critical for cardiac fibrosis were examined, namely, NLRP3, MMP2, MMP9, CCN2/CTGF, AGT (encodes angiotensin II precursors) and hsa-mir-223 (post-transcriptionally regulates NLRP3). Results: In monocytes, neutrophils, fibroblasts, venous cells, liver and brain, enhancers or super-enhancers were found that correlate with high expression of these genes. One enhancer extended into a silent gene neighbor. These enhancers harbored tissue-specific foci of DNA hypomethylation, open chromatin and transcription factor binding. Conclusions: This study identified previously undescribed enhancers containing hypomethylated transcription factor binding subregions that are predicted to regulate expression of these cardiac fibrosis-inducing genes.

Keywords: DNA methylation; DNase I hypersensitive sites; cardiovascular disease; enhancers; epigenetics; fibrosis; inflammasomes; lincRNA; super-enhancers; transcription factor binding.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Angiotensin II / genetics
  • Angiotensin II / metabolism
  • Aorta / metabolism
  • Connective Tissue Growth Factor / genetics
  • Connective Tissue Growth Factor / metabolism
  • DNA Methylation
  • Enhancer Elements, Genetic*
  • Epigenesis, Genetic*
  • Female
  • Fibrosis
  • Gene Expression
  • Humans
  • Liver / metabolism
  • Male
  • Matrix Metalloproteinase 2 / genetics
  • Matrix Metalloproteinase 2 / metabolism
  • Matrix Metalloproteinase 9 / genetics
  • Matrix Metalloproteinase 9 / metabolism
  • MicroRNAs / metabolism
  • Monocytes / metabolism
  • Myocardium / pathology*
  • NLR Family, Pyrin Domain-Containing 3 Protein / genetics
  • NLR Family, Pyrin Domain-Containing 3 Protein / metabolism
  • Neutrophils / metabolism

Substances

  • MicroRNAs
  • NLR Family, Pyrin Domain-Containing 3 Protein
  • Angiotensin II
  • Connective Tissue Growth Factor
  • Matrix Metalloproteinase 2
  • Matrix Metalloproteinase 9