Comparative analysis of the mechanical signals in lung development and compensatory growth

Cell Tissue Res. 2017 Mar;367(3):687-705. doi: 10.1007/s00441-016-2558-8. Epub 2017 Jan 13.

Abstract

This review compares the manner in which physical stress imposed on the parenchyma, vasculature and thorax and the thoraco-pulmonary interactions, drive both developmental and compensatory lung growth. Re-initiation of anatomical lung growth in the mature lung is possible when the loss of functioning lung units renders the existing physiologic-structural reserves insufficient for maintaining adequate function and physical stress on the remaining units exceeds a critical threshold. The appropriate spatial and temporal mechanical interrelationships and the availability of intra-thoracic space, are crucial to growth initiation, follow-on remodeling and physiological outcome. While the endogenous potential for compensatory lung growth is retained and may be pharmacologically augmented, supra-optimal mechanical stimulation, unbalanced structural growth, or inadequate remodeling may limit functional gain. Finding ways to optimize the signal-response relationships and resolve structure-function discrepancies are major challenges that must be overcome before the innate compensatory ability could be fully realized. Partial pneumonectomy reproducibly removes a known fraction of functioning lung units and remains the most robust model for examining the adaptive mechanisms, structure-function consequences and plasticity of the remaining functioning lung units capable of regeneration. Fundamental mechanical stimulus-response relationships established in the pneumonectomy model directly inform the exploration of effective approaches to maximize compensatory growth and function in chronic destructive lung diseases, transplantation and bioengineered lungs.

Keywords: Lung development; Lung regeneration; Mechanical stress; Mechanotransduction; Pneumonectomy.

Publication types

  • Comparative Study
  • Review

MeSH terms

  • Animals
  • Lung / growth & development*
  • Lung / metabolism*
  • Mechanotransduction, Cellular*
  • Regeneration
  • Signal Transduction*
  • Translational Research, Biomedical