Preconditioning of physiological cyclic stretch attenuated HMGB1 expression in pathologically mechanical stretch-activated A549 cells and ventilator-induced lung injury rats through inhibition of IL-6/STAT3/SOCS3

Int Immunopharmacol. 2016 Feb:31:66-73. doi: 10.1016/j.intimp.2015.12.017. Epub 2015 Dec 17.

Abstract

Previous studies have shown that physiologically cyclic stretch (5% CS) attenuated both oxidative- and LPS-induced increases in HMGB1 expression via STAT3. However, little information exists about the effect of precondition of physiological cyclic stretch (CS) on the expression of HMGB 1, which play a crucial role in ventilator-induced lung injury (VILI). We found that 5% CS-preconditioning significantly inhibited HMGB 1 expression, but not HMGB 1 receptors. 5% CS-preconditioning inhibits the IL-6/STAT3 pathway, and the inhibitory effect on the expression of HMGB 1 induced by 5% CS-preconditioning is abolished by additional treatment of rmIL-6. 5% CS-preconditioning also induces SOCS3 upregulation, and 5% CS-preconditioning fails to inhibit the IL-6/STAT3 pathway in cells transfected with SOCS3 siRNA. Moreover, low tidal volume ventilation preconditioning also decreases the severity of VILI evidenced by the markedly improved pulmonary alveolar-capillary barrier dysfunction, wet/dry weight ratio, and histological analysis. These results suggest that preconditioning of physiological 5% CS can reduce the expression of HMGB 1 induced by pathologically mechanical stretch through IL-6/STAT3 pathway associated with up-regulated SOCS3 expression.

Keywords: IL-6/STAT3; Lung injury; Mechanical ventilation; Preconditioning; SOCS3.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Female
  • Gene Expression Regulation / genetics
  • HMGB1 Protein / genetics
  • HMGB1 Protein / metabolism*
  • Humans
  • Interleukin-6 / metabolism
  • Lung / physiology*
  • Physical Conditioning, Animal
  • RNA, Small Interfering / genetics
  • Rats
  • Rats, Wistar
  • Respiration, Artificial* / adverse effects
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction / genetics
  • Suppressor of Cytokine Signaling 3 Protein / genetics
  • Suppressor of Cytokine Signaling 3 Protein / metabolism*
  • Tidal Volume
  • Ventilator-Induced Lung Injury / prevention & control*

Substances

  • HMGB1 Protein
  • Interleukin-6
  • RNA, Small Interfering
  • STAT3 Transcription Factor
  • Socs3 protein, rat
  • Suppressor of Cytokine Signaling 3 Protein