DOCK2 Promotes Pleural Fibrosis by Modulating Mesothelial to Mesenchymal Transition

Guoqing Qian1, Oluwaseun Adeyanju1, Saptarshi Roy1

  • 1Department of Cellular and Molecular Biology, The University of Texas Health Science Center at Tyler, Tyler, Texas; and.

Insights

Dedicator of cytokinesis 2 (DOCK2) drives pleural fibrosis by promoting mesothelial to mesenchymal transition (MesoMT). Inhibiting DOCK2 may offer a new therapeutic strategy for this restrictive lung disease.

Area of Science:

  • Pulmonary Medicine
  • Cell Biology
  • Molecular Biology

Background:

  • Pleural fibrosis causes restrictive lung disease via mesothelial to mesenchymal transition (MesoMT).
  • The role of Dedicator of cytokinesis 2 (DOCK2) in pleural fibrosis and MesoMT is currently unknown.
  • DOCK2 is known for its immune function roles.

Purpose of the Study:

  • To investigate the role of DOCK2 in the pathogenesis of pleural fibrosis, specifically its involvement in MesoMT.
  • To explore DOCK2 as a potential therapeutic target for pleural fibrosis.

Main Methods:

  • Analysis of DOCK2 and MesoMT markers (α-SMA) in human pleural biopsy samples and three animal models of pleural fibrosis.
  • In vivo studies using DOCK2-knockout mice subjected to Streptococcus pneumoniae infection.
  • In vitro experiments involving primary human pleural mesothelial cells treated with transforming growth factor-β (TGF-β) and DOCK2 knockdown.

Main Results:

  • DOCK2 and α-SMA were significantly elevated and colocalized in fibrotic pleura of patients and animal models.
  • DOCK2-knockout mice showed protection against Streptococcus pneumoniae-induced pleural fibrosis.
  • TGF-β induced DOCK2 expression and MesoMT markers in vitro, which were attenuated by DOCK2 knockdown, also inhibiting Snail upregulation.

Conclusions:

  • DOCK2 is upregulated in pleural fibrosis and mediates MesoMT.
  • DOCK2 plays a critical role in the pathogenesis of pleural fibrosis by promoting neomatrix deposition.
  • DOCK2 represents a potential novel therapeutic target for preventing or treating pleural fibrosis.