Neutrophil Gelatinase-Associated Lipocalin, a Novel Mineralocorticoid Biotarget, Mediates Vascular Profibrotic Effects of Mineralocorticoids

Hypertension. 2015 Jul;66(1):158-66. doi: 10.1161/HYPERTENSIONAHA.115.05431. Epub 2015 May 18.

Abstract

Activation of the mineralocorticoid receptor has been shown to be deleterious in cardiovascular diseases (CVDs). We have recently shown that lipocalin 2 (Lcn2), or neutrophil gelatinase-associated lipocalin (NGAL), is a primary target of aldosterone/mineralocorticoid receptor in the cardiovascular system. Lcn2 is a circulating protein, which binds matrix metalloproteinase 9 and modulates its stability. We hypothesized that Lcn2 could be a mediator of aldosterone/mineralocorticoid receptor profibrotic effects in the cardiovascular system. Correlations between aldosterone and profibrotic markers, such as procollagen type I N-terminal peptide, were investigated in healthy subjects and subjects with abdominal obesity. The implication of Lcn2 in the mineralocorticoid pathway was studied using Lcn2 knockout mice subjected to a nephrectomy/aldosterone/salt (NAS) challenge for 4 weeks. In human subjects, NGAL/matrix metalloproteinase 9 was positively correlated with plasma aldosterone and fibrosis biomarkers. In mice, loss of Lcn2 prevented the NAS-induced increase of plasma procollagen type I N-terminal peptide, as well as the increase of collagen fibers deposition and collagen I expression in the coronary vessels and the aorta. The lack of Lcn2 also blunted the NAS-induced increase in systolic blood pressure. Ex vivo, treatment of human fibroblasts with recombinant Lcn2 induced the expression of collagen I and the profibrotic galectin-3 and cardiotrophin-1 molecules. Our results showed that Lcn2 plays a key role in aldosterone/mineralocorticoid receptor-mediated vascular fibrosis. The clinical data indicate that this may translate in human patients. Lcn2 is, therefore, a new biotarget in cardiovascular fibrosis induced by mineralocorticoid activation.

Keywords: aldosterone; collagen type I; fibroblast; lipocalin 2; mineralocorticoid receptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute-Phase Proteins / deficiency
  • Acute-Phase Proteins / genetics
  • Acute-Phase Proteins / pharmacology
  • Acute-Phase Proteins / physiology*
  • Aldosterone / blood
  • Aldosterone / toxicity*
  • Animals
  • Aorta / drug effects
  • Aorta / pathology
  • Cardiomyopathy, Hypertrophic / chemically induced
  • Cardiomyopathy, Hypertrophic / physiopathology
  • Cells, Cultured
  • Cytokines / biosynthesis
  • Cytokines / genetics
  • Female
  • Fibroblasts
  • Fibrosis
  • Galectin 3 / biosynthesis
  • Galectin 3 / blood
  • Galectin 3 / genetics
  • Humans
  • Hypertension / physiopathology
  • Hypertrophy
  • Kidney / pathology
  • Lipocalin-2
  • Lipocalins / blood
  • Lipocalins / genetics
  • Lipocalins / pharmacology
  • Lipocalins / physiology*
  • Male
  • Mice
  • Myocardium / cytology
  • Myocardium / metabolism
  • Myocytes, Smooth Muscle / drug effects
  • Myocytes, Smooth Muscle / physiology
  • Nephrectomy / adverse effects
  • Obesity, Abdominal / blood
  • Obesity, Abdominal / physiopathology*
  • Oncogene Proteins / deficiency
  • Oncogene Proteins / genetics
  • Oncogene Proteins / physiology*
  • Peptide Fragments / blood
  • Procollagen / blood
  • Proto-Oncogene Proteins / blood
  • Proto-Oncogene Proteins / pharmacology
  • Proto-Oncogene Proteins / physiology*
  • Rats
  • Recombinant Proteins / pharmacology

Substances

  • Acute-Phase Proteins
  • Cytokines
  • Galectin 3
  • LCN2 protein, human
  • Lipocalin-2
  • Lipocalins
  • Oncogene Proteins
  • Peptide Fragments
  • Procollagen
  • Proto-Oncogene Proteins
  • Recombinant Proteins
  • procollagen Type I N-terminal peptide
  • procollagen Type III-N-terminal peptide
  • Lcn2 protein, mouse
  • Aldosterone
  • cardiotrophin 1