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Author Notes:

Nadir Yehya: yehyan@email.chop.edu; Tel.: +1-215-590-5907

N.Y. and S.S.M. were responsible for conceptualization and funding.

M.J.S. and G.G.L. performed cell experiments and Western blots.

N.Y. performed animal experiments.

N.Y. and S.S.M. performed data analysis.

N.Y. wrote the first draft of the manuscript, and all authors edited and approved the final version.

The authors are grateful to Jesi Kim and Nurit Davidovich for cell preparation, assistance with immunoprecipitation and Western blotting, and for assistance with the manuscript.

The authors declare no conflict of interest, and the funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

Subjects:

Research Funding:

This research was funded by the George H. Stephenson Endowed Chair, Department of Bioengineering, University of Pennsylvania (S.S.M.); NIH NHLBI R01-HL57204 (S.S.M.); NIH NHLBI K12-HL109009 (N.Y.); NIH NHLBI K23-HL136688 (N.Y.).

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Physical Sciences
  • Biochemistry & Molecular Biology
  • Chemistry, Multidisciplinary
  • Chemistry
  • ventilator-induced lung injury
  • VILI
  • HER2
  • HER3
  • neuregulin-1
  • NRG1
  • RESPIRATORY-DISTRESS-SYNDROME
  • LUNG-PROTECTIVE VENTILATION
  • DEFORMATION-INDUCED INJURY
  • LOWER TIDAL VOLUMES
  • CELLS
  • NEUREGULIN-1
  • ACTIVATION
  • PATHWAYS
  • DURATION

HER2 Signaling Implicated in Regulating Alveolar Epithelial Permeability with Cyclic Stretch

Tools:

Journal Title:

International Journal of Molecular Sciences

Volume:

Volume 20, Number 4

Publisher:

Type of Work:

Article | Final Publisher PDF

Abstract:

Mechanical ventilation can be damaging, and can cause or exacerbate ventilator-induced lung injury (VILI). The human epidermal growth factor receptor (HER) ligand neuregulin-1 (NRG1) activates HER2 heterodimerization with HER3, and has been implicated in inflammatory injuries. We hypothesized that HER2 activation contributes to VILI.We analyzed a database of differentially expressed genes between cyclically stretched and unstretched rat alveolar epithelial cells (RAEC) for HER ligands and validated the differential expression. The effect of the ligand and HER2 inhibition on RAEC permeability was tested, and in vivo relevance was assessed in a rat model of VILI. Analysis of our expression array revealed the upregulation of NRG1 and amphiregulin (AREG) with stretch. NRG1 protein, but not AREG, increased after stretch in culture media. Treatment with an NRG1-cleavage inhibitor (TAPI2) or an inhibitor of NRG1-binding (anti-HER3 antibody) reduced HER2 phosphorylation and partially mitigated stretch-induced permeability, with the upregulation of claudin-7. The results were reproduced by treatment with a direct inhibitor of HER2 phosphorylation (AG825). The transfection of microRNA miR-15b, predicted to negatively regulate NRG1, also attenuated stretch-induced permeability, and was associated with lower NRG1 mRNA levels. In rats ventilated at damaging tidal volumes, AG825 partly attenuated VILI.We concluded that cyclic stretch activates HER2 via the HER3 ligand NRG1, leading to increased permeability. Outcomes were mitigated by the downregulation of NRG1, prevention of NRG1 binding, and most strongly by the direct inhibition of HER2. In vivo HER2 inhibition also attenuated VILI. Ligand-dependent HER2 activation is a potential target for reducing VILI.

Copyright information:

© 2019 by the authors. Licensee MDPI, Basel, Switzerland.

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).
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