HIF-1α promotes the keloid development through the activation of TGF-β/Smad and TLR4/MyD88/NF-κB pathways

Cell Cycle. 2019 Dec;18(23):3239-3250. doi: 10.1080/15384101.2019.1670508. Epub 2019 Oct 23.

Abstract

A keloid is defined as an overgrowth of the dense fibrous tissues that form around a wound. Since they destroy the vascular network, keloid tissues often exhibit anoxic conditions. Hypoxia-inducible factor-1α (HIF-1α) is a core factor that mediates hypoxia stress responses and regulates the hypoxic cellular and biological behaviors. In this study, we found that the expression level of HIF-1α in keloid tissue was significantly higher than that in the normal skin tissue. Hypoxia-induced HIF-1α expression significantly inhibited cellular apoptosis and promoted cellular proliferation in keloid fibroblasts but not in normal fibroblasts. Specifically, HIF-1α activated the TGF-β/Smad and TLR4/MyD88/NF-κB pathways, and the interaction of these two pathways may promote the development of keloids. Moreover, in vivo experiments showed that the inhibition of HIF-1α significantly reduced the growth of keloids.

Keywords: HIF-1α; NF-κB; TGF-β/Smad; TLR4; fibroblasts; keloid.

MeSH terms

  • Animals
  • Apoptosis / genetics
  • Cell Hypoxia / genetics
  • Cell Proliferation / genetics
  • Fibroblasts / metabolism
  • Gene Expression Regulation / genetics
  • Heterografts
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit / genetics*
  • Keloid / genetics*
  • Keloid / pathology
  • Mice
  • Myeloid Differentiation Factor 88 / genetics*
  • Primary Cell Culture
  • Signal Transduction / genetics
  • Smad Proteins / genetics
  • Toll-Like Receptor 4 / genetics*
  • Transcription Factor RelA / genetics
  • Transforming Growth Factor beta / genetics

Substances

  • HIF1A protein, human
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Myeloid Differentiation Factor 88
  • RELA protein, human
  • Smad Proteins
  • TLR4 protein, human
  • Toll-Like Receptor 4
  • Transcription Factor RelA
  • Transforming Growth Factor beta

Grants and funding

This study was supported by project grants from the National Natural Science Foundation of China (81873937).