[New insights in the pathogenesis of pulmonary arterial hypertension]

Rev Mal Respir. 2019 Apr;36(4):433-437. doi: 10.1016/j.rmr.2019.03.003. Epub 2019 Apr 19.
[Article in French]

Abstract

Pulmonary arterial hypertension (PAH) is a severe and incurable cardiopulmonary disorder. Research from the past 10 years illustrates the complex and multifactorial aspects of PAH pathophysiology. Furthermore, latest advances in the field have led to a better understanding of the key components underlying this inadequate accumulation of pulmonary vascular cells within the pulmonary arterial walls, leading to pulmonary vascular remodelling. Among the underlying molecular and cellular mechanisms, pulmonary endothelial dysfunction, alterations of the inter-cell communications within the pulmonary arterial walls as well as defects of the inflammatory component and the loss of BMPRII activity play critical roles in the pathogenesis of the disease.

Keywords: Cellule musculaire lisse; Cible thérapeutique; Hypertension pulmonaire; Pulmonary hypertension; Remodelage vasculaire pulmonaire; Smooth muscle cell; Therapeutic target; Vascular remodelling.

Publication types

  • Review

MeSH terms

  • Adaptive Immunity / physiology
  • Autoimmunity / physiology
  • Bone Morphogenetic Protein Receptors, Type II / genetics
  • Bone Morphogenetic Protein Receptors, Type II / metabolism
  • Endothelial Cells / physiology
  • Humans
  • Hypertension, Pulmonary / etiology
  • Hypertension, Pulmonary / genetics
  • Hypertension, Pulmonary / immunology
  • Hypertension, Pulmonary / physiopathology
  • Molecular Targeted Therapy / methods
  • Molecular Targeted Therapy / trends
  • Myocytes, Smooth Muscle / physiology
  • Pulmonary Arterial Hypertension / etiology*
  • Pulmonary Arterial Hypertension / genetics
  • Pulmonary Arterial Hypertension / immunology
  • Pulmonary Arterial Hypertension / physiopathology
  • Pulmonary Artery / pathology
  • Pulmonary Artery / physiology
  • Signal Transduction / genetics
  • Vascular Remodeling / physiology

Substances

  • BMPR2 protein, human
  • Bone Morphogenetic Protein Receptors, Type II