E2F transcription factor 1 (E2F1) promotes the transforming growth factor TGF-β1 induced human cardiac fibroblasts differentiation through promoting the transcription of CCNE2 gene

Bioengineered. 2021 Dec;12(1):6869-6877. doi: 10.1080/21655979.2021.1972194.

Abstract

The differentiation of cardiac fibroblast to myofibroblast is the key process of cardiac fibrosis. In the study, we aimed to determine the function of E2F Transcription Factor 1 (E2F1) in human cardiac fibroblasts (HCFs) differentiation, search for its downstream genes and elucidate the function of them in HCFs differentiation. As a result, we found that E2F1 was up-regulated in TGF-β1-induced HCFs differentiation. Silencing the expression of E2F1 by siRNA in HCFs, we found that the expression of differentiation-related genes (Collagen-1, α-Smooth muscle actin, and Fibronectin-1) was significantly suppressed, combining with proliferation and migration assay, we determined that HCFs differentiation was decreased. Luciferase report assay and immunoprecipitation proved that the oncogene CCNE2 was a direct target gene of E2F1, overexpression of CCNE2 was found in differentiated HCFs, silencing the expression of CCNE2 by siRNA decreased HCFs differentiation. Our research suggested that E2F1 and its downstream target gene CCNE2 play a vital role in TGF-β1-induced HCFs differentiation, thus E2F1 and CCNE2 may be a potential therapeutic target for cardiac fibrosis.

Keywords: CCNE2; Cardiac fibrosis; E2F1; human cardiac fibroblasts; myocardial infarction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Differentiation / drug effects
  • Cell Differentiation / genetics*
  • Cells, Cultured
  • Cyclins / genetics*
  • Cyclins / metabolism
  • E2F1 Transcription Factor / genetics*
  • E2F1 Transcription Factor / metabolism
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism
  • Humans
  • Myocardium / cytology*
  • Transcription, Genetic / genetics
  • Transforming Growth Factor beta1 / pharmacology

Substances

  • CCNE2 protein, human
  • Cyclins
  • E2F1 Transcription Factor
  • E2F1 protein, human
  • Transforming Growth Factor beta1

Grants and funding

This work was supported by the grants from National Natural Science Foundation of China (81770339). The funding bodies played no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.