Poldip2 deficiency protects against lung edema and vascular inflammation in a model of acute respiratory distress syndrome

Clin Sci (Lond). 2019 Jan 25;133(2):321-334. doi: 10.1042/CS20180944. Print 2019 Jan 31.

Abstract

Acute respiratory distress syndrome (ARDS) in a deadly disease that can be brought on by endotoxins such as lipopolysaccharide (LPS). ARDS is characterized by vascular permeability, a severe inflammatory response, lung leukocyte infiltration, and resultant lung edema. Polymerase δ-interacting protein 2 (Poldip2) is a novel regulator of blood-brain barrier permeability; however, its role in regulating lung permeability and vascular inflammation is unknown. Here, the role of Poldip2 in regulating vascular permeability and inflammation in a mouse model of ARDS was assessed. Heterozygous deletion of Poldip2 was found to reduce LPS-induced mortality within 20 h, lung inflammatory signaling, and leukocyte infiltration. Moreover, reduced Poldip2-suppressed LP-induced vascular cell adhesion molecule (VCAM)-1 induction, leukocyte recruitment, and mitochondrial reactive oxygen species (ROS) production in vitro These data indicate that Poldip2 is an important regulator of the debilitating consequences of ARDS, potentially through the regulation of mitochondrial ROS-induced inflammatory signaling. Consequently, inhibition of Poldip2 may be a viable option for therapeutic discovery moving forward.

Keywords: Poldip2; acute respiratory distress syndrome; inflammation; leukocyte.

Publication types

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

MeSH terms

  • Animals
  • Capillary Permeability*
  • Cell Adhesion
  • Coculture Techniques
  • Cytokines / metabolism
  • Disease Models, Animal
  • Endothelial Cells / metabolism*
  • Endothelial Cells / pathology
  • Female
  • Humans
  • Leukocytes / metabolism
  • Leukocytes / pathology
  • Lung / blood supply*
  • Male
  • Mice, Inbred C57BL
  • Mitochondrial Proteins / deficiency*
  • Mitochondrial Proteins / genetics
  • Nuclear Proteins / deficiency*
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism
  • Pulmonary Edema / genetics
  • Pulmonary Edema / metabolism
  • Pulmonary Edema / pathology
  • Pulmonary Edema / prevention & control*
  • Reactive Oxygen Species / metabolism
  • Respiratory Distress Syndrome / genetics
  • Respiratory Distress Syndrome / metabolism*
  • Respiratory Distress Syndrome / pathology
  • Signal Transduction
  • THP-1 Cells
  • Vascular Cell Adhesion Molecule-1 / metabolism
  • Vasculitis / genetics
  • Vasculitis / metabolism
  • Vasculitis / pathology
  • Vasculitis / prevention & control*

Substances

  • Cytokines
  • Mitochondrial Proteins
  • Nuclear Proteins
  • POLDIP2 protein, human
  • Reactive Oxygen Species
  • Vascular Cell Adhesion Molecule-1
  • mitogenin 1 protein, mouse