PGC-1α mediates a metabolic host defense response in human airway epithelium during rhinovirus infections

Nat Commun. 2021 Jun 16;12(1):3669. doi: 10.1038/s41467-021-23925-z.

Abstract

Human rhinoviruses (HRV) are common cold viruses associated with exacerbations of lower airways diseases. Although viral induced epithelial damage mediates inflammation, the molecular mechanisms responsible for airway epithelial damage and dysfunction remain undefined. Using experimental HRV infection studies in highly differentiated human bronchial epithelial cells grown at air-liquid interface (ALI), we examine the links between viral host defense, cellular metabolism, and epithelial barrier function. We observe that early HRV-C15 infection induces a transitory barrier-protective metabolic state characterized by glycolysis that ultimately becomes exhausted as the infection progresses and leads to cellular damage. Pharmacological promotion of glycolysis induces ROS-dependent upregulation of the mitochondrial metabolic regulator, peroxisome proliferator-activated receptor-γ coactivator 1α (PGC-1α), thereby restoring epithelial barrier function, improving viral defense, and attenuating disease pathology. Therefore, PGC-1α regulates a metabolic pathway essential to host defense that can be therapeutically targeted to rescue airway epithelial barrier dysfunction and potentially prevent severe respiratory complications or secondary bacterial infections.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Synthetase Complexes / antagonists & inhibitors
  • ATP Synthetase Complexes / metabolism
  • Antiviral Agents / metabolism*
  • Antiviral Agents / pharmacology
  • Cell Culture Techniques
  • Cytoskeleton / metabolism
  • Epithelial Cells
  • Fatty Acids / biosynthesis
  • Glycolysis
  • Humans
  • Metabolic Networks and Pathways
  • Mitochondria / metabolism
  • Oligomycins / pharmacology
  • Oxygen Consumption / drug effects
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha / genetics
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha / metabolism*
  • Picornaviridae Infections / virology
  • Reactive Oxygen Species / metabolism
  • Respiratory Mucosa / drug effects
  • Respiratory Mucosa / metabolism*
  • Respiratory Mucosa / pathology
  • Respiratory Mucosa / virology
  • Rhinovirus / physiology*
  • Virus Replication / drug effects

Substances

  • Antiviral Agents
  • Fatty Acids
  • Oligomycins
  • PPARGC1A protein, human
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Reactive Oxygen Species
  • oligomycin A
  • ATP Synthetase Complexes

Grants and funding