Article Text

Download PDFPDF
Retinoid induction of alveolar regeneration: from mice to man?
  1. M Hind1,2,
  2. Å Gilthorpe2,
  3. S Stinchcombe2,
  4. M Maden2
  1. 1
    Department of Respiratory Medicine, Royal Brompton Hospital and National Heart and Lung Institute, Imperial College London, London, UK
  2. 2
    MRC Centre for Developmental Neurobiology, King’s College London, London, UK
  1. Dr M Hind, Department of Respiratory Medicine, Royal Brompton Hospital and National Heart and Lung Institute, Imperial College London, London SW3 6NP, UK; m.hind{at}imperial.ac.uk

Abstract

The use of retinoids to induce human lung regeneration is under investigation in a number of studies in patients with chronic obstructive pulmonary disease (COPD). Retinoic acid (RA) has complex pleiotropic functions during vertebrate patterning and development and can induce regeneration in a number of different organ systems. Studies of retinoid signalling during lung development might provide a molecular basis to explain pharmacological induction of alveolar regeneration in adult models of lung disease. In this review the role of endogenous RA signalling during alveologenesis is explored and data suggesting that a number of exogenous retinoids can induce regeneration in the adult lung are discussed. Current controversies in this area are highlighted and a hypothesis of lung regeneration is put forward. Understanding the cellular and molecular mechanisms of induction of regeneration will be central for effective translation into patients with lung disease and may reveal novel insights into the pathogenesis of alveolar disease and senescence.

Statistics from Altmetric.com

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Footnotes

  • Funding: This work was supported by a Wellcome Training Fellowship (MH), a Wellcome Trust project grant (MM and MH), Wellcome VIP Award (ÅG) and an MRC Clinical Fellowship (SS).

  • Competing interests: None.