Functional contribution of sphingosine-1-phosphate to airway pathology in cigarette smoke-exposed mice

Br J Pharmacol. 2020 Jan;177(2):267-281. doi: 10.1111/bph.14861. Epub 2019 Nov 6.

Abstract

Background and purpose: A critical role for sphingosine kinase/sphingosine-1-phosphate (S1P) pathway in the control of airway function has been demonstrated in respiratory diseases. Here, we address S1P contribution in a mouse model of mild chronic obstructive pulmonary disease (COPD).

Experimental approach: C57BL/6J mice have been exposed to room air or cigarette smoke up to 11 months and killed at different time points. Functional and molecular studies have been performed.

Key results: Cigarette smoke caused emphysematous changes throughout the lung parenchyma coupled to a progressive collagen deposition in both peribronchiolar and peribronchial areas. The high and low airways showed an increased reactivity to cholinergic stimulation and α-smooth muscle actin overexpression. Similarly, an increase in airway reactivity and lung resistances following S1P challenge occurred in smoking mice. A high expression of S1P, Sph-K2 , and S1P receptors (S1P2 and S1P3 ) has been detected in the lung of smoking mice. Sphingosine kinases inhibition reversed the increased cholinergic response in airways of smoking mice.

Conclusions and implications: S1P signalling up-regulation follows the disease progression in smoking mice and is involved in the development of airway hyperresponsiveness. Our study defines a therapeutic potential for S1P inhibitors in management of airways hyperresponsiveness associated to emphysema in smokers with both asthma and COPD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Airway Remodeling*
  • Animals
  • Bronchial Hyperreactivity / etiology
  • Bronchial Hyperreactivity / metabolism*
  • Bronchial Hyperreactivity / pathology
  • Bronchial Hyperreactivity / physiopathology
  • Bronchoconstriction*
  • Cigarette Smoking / adverse effects*
  • Collagen / metabolism
  • Disease Models, Animal
  • Lung / metabolism*
  • Lung / pathology
  • Lung / physiopathology
  • Lysophospholipids / metabolism*
  • Mice, Inbred C57BL
  • Phosphotransferases (Alcohol Group Acceptor) / metabolism
  • Pulmonary Disease, Chronic Obstructive / etiology
  • Pulmonary Disease, Chronic Obstructive / metabolism*
  • Pulmonary Disease, Chronic Obstructive / pathology
  • Pulmonary Disease, Chronic Obstructive / physiopathology
  • Pulmonary Emphysema / etiology
  • Pulmonary Emphysema / metabolism*
  • Pulmonary Emphysema / pathology
  • Pulmonary Emphysema / physiopathology
  • Signal Transduction
  • Smoke
  • Sphingosine / analogs & derivatives*
  • Sphingosine / metabolism
  • Sphingosine-1-Phosphate Receptors / metabolism
  • Time Factors
  • Tobacco Products

Substances

  • Actins
  • Lysophospholipids
  • S1pr1 protein, mouse
  • Smoke
  • Sphingosine-1-Phosphate Receptors
  • alpha-smooth muscle actin, mouse
  • sphingosine-1-phosphate receptor-2, mouse
  • sphingosine 1-phosphate
  • Collagen
  • Phosphotransferases (Alcohol Group Acceptor)
  • sphingosine kinase 2, mouse
  • Sphingosine