Ezrin regulates synovial angiogenesis in rheumatoid arthritis through YAP and Akt signalling

J Cell Mol Med. 2021 Oct;25(19):9378-9389. doi: 10.1111/jcmm.16877. Epub 2021 Aug 29.

Abstract

This study aimed to investigate the role and regulatory mechanisms of Ezrin in synovial vessels in rheumatoid arthritis (RA). Synovial tissues were obtained from people with osteoarthritis people and patients with RA patients. We also used an antigen-induced arthritis (AIA) mice model by using Freund's adjuvant injections. Ezrin expression was analysed by immunofluorescence and immunohistochemical staining in synovial vessels of patients with RA and AIA mice. We investigated the role of Ezrin on vascular endothelial cells and its regulatory mechanism in vivo and in vitro by adenoviral transfection technology. Our results suggest a role for the Ezrin protein in proliferation, migration and angiogenesis of vascular endothelial cells in RA. We also demonstrate that Ezrin plays an important role in vascular endothelial cell migration and tube formation through regulation of the Hippo-yes-associated protein 1 (YAP) pathway. YAP, as a key protein, can further regulate the activity of PI3K/Akt signalling pathway in vascular endothelial cells. In AIA mice experiments, we observed that the inhibition of Ezrin or of its downstream YAP pathway can affect synovial angiogenesis and may lead to progression of RA. In conclusion, Ezrin plays an important role in angiogenesis in the RA synovium by regulating YAP nuclear translocation and interacting with the PI3K/Akt signalling pathway.

Keywords: Ezrin; Hippo-YAP; PI3K/Akt; angiogenesis; rheumatoid arthritis.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Animals
  • Arthritis, Rheumatoid / etiology*
  • Arthritis, Rheumatoid / metabolism*
  • Arthritis, Rheumatoid / pathology
  • Biomarkers
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism*
  • Cell Line
  • Cells, Cultured
  • Cytoskeletal Proteins / genetics*
  • Cytoskeletal Proteins / metabolism
  • Disease Models, Animal
  • Disease Progression
  • Disease Susceptibility
  • Female
  • Gene Expression
  • Humans
  • Immunohistochemistry
  • Male
  • Mice
  • Middle Aged
  • Neovascularization, Pathologic / genetics
  • Neovascularization, Pathologic / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Severity of Illness Index
  • Signal Transduction
  • Synovial Membrane / blood supply*
  • Synovial Membrane / metabolism*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*

Substances

  • Biomarkers
  • Cell Cycle Proteins
  • Cytoskeletal Proteins
  • Transcription Factors
  • YY1AP1 protein, human
  • ezrin
  • Proto-Oncogene Proteins c-akt