Complex roles of TGF-β signaling pathways in lung development and bronchopulmonary dysplasia

Author:

Calthorpe Rebecca J.12ORCID,Poulter Caroline3,Smyth Alan R.12ORCID,Sharkey Don4ORCID,Bhatt Jayesh3ORCID,Jenkins Gisli5ORCID,Tatler Amanda L.2ORCID

Affiliation:

1. Lifespan & Population Health, School of Medicine, University of Nottingham, Nottingham, United Kingdom

2. NIHR Nottingham Biomedical Research Centre, Biodiscovery Institute, University of Nottingham, Nottingham, United Kingdom

3. Department of Pediatrics, Queens Medical Centre, Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom

4. Centre for Perinatal Research, School of Medicine, University of Nottingham, Nottingham, United Kingdom

5. National Heart and Lung Institute, Imperial College London, London, United Kingdom

Abstract

As survival of extremely preterm infants continues to improve, there is also an associated increase in bronchopulmonary dysplasia (BPD), one of the most significant complications of preterm birth. BPD development is multifactorial resulting from exposure to multiple antenatal and postnatal stressors. BPD has both short-term health implications and long-term sequelae including increased respiratory, cardiovascular, and neurological morbidity. Transforming growth factor β (TGF-β) is an important signaling pathway in lung development, organ injury, and fibrosis and is implicated in the development of BPD. This review provides a detailed account on the role of TGF-β in antenatal and postnatal lung development, the effect of known risk factors for BPD on the TGF-β signaling pathway, and how medications currently in use or under development, for the prevention or treatment of BPD, affect TGF-β signaling.

Funder

Medical Research Foundation

National Institute for Health and Care Research

Publisher

American Physiological Society

Subject

Cell Biology,Physiology (medical),Pulmonary and Respiratory Medicine,Physiology

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