Selective upregulation of cardiac brain natriuretic peptide at the transcriptional and translational levels by pro-inflammatory cytokines and by conditioned medium derived from mixed lymphocyte reactions via p38 MAP kinase

J Mol Cell Cardiol. 2004 Apr;36(4):505-13. doi: 10.1016/j.yjmcc.2004.01.001.

Abstract

An increase in circulating brain natriuretic peptide (BNP) but not atrial natriuretic factor (ANF) is observed coincident with cardiac allograft rejection that is reversed upon treatment with anti-lymphocyte therapy suggesting that pro-inflammatory cytokines may uniquely modulate BNP gene expression and secretion. This study tested pro-inflammatory cytokines or conditioned medium (CM) derived from mixed- lymphocyte reaction (MLR) cultures in their ability to modulate ANF or BNP mRNA expression, secretion, as well as BNP promoter activity in cultured neonatal rat cardiocytes. IL-1 beta and TNF-alpha elicited a significant dose- and time-dependent increase in BNP mRNA, and secretion, whereas, ANF mRNA levels and secretion did not change. IL-1 beta and TNF-alpha rapidly increased phosphorylated p38 MAP kinase abundance and activity. Inhibition of p38 MAP kinase with SB203580 abolished IL-1 beta- and TNF-alpha-stimulated increase in BNP mRNA, promoter activity and secretion. MLR-CM in 20%, 50% and 100% proportions increased BNP but not ANF secretion. The MLR-induced increases in BNP secretion were completely abolished by SB203580 pre-treatment. These investigations show that exposure of cultured rat cardiocytes to specific pro-inflammatory cytokines as well as MLR-CM results in the only known instance of upregulation of cardiac BNP at the transcriptional and translational levels without a corresponding increase in ANF gene expression. Furthermore, these effects are dependent on signaling by p38 MAP kinase. In all, the findings reveal a unique dis-coordinated expression of BNP and ANF to inflammatory cytokines and offers an opportunity to better understand the differential regulation of these two cardiac-derived endocrine hormones that share receptors as well as biological properties.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Blotting, Northern
  • Blotting, Western
  • Cells, Cultured
  • Culture Media, Conditioned / pharmacology*
  • Cytokines / biosynthesis*
  • Densitometry
  • Dose-Response Relationship, Drug
  • Enzyme Activation
  • Gene Expression Regulation
  • Imidazoles / pharmacology
  • Inflammation
  • Interferon-gamma / metabolism
  • Interleukin-1 / metabolism
  • Lymphocytes / immunology*
  • Myocardium / metabolism*
  • Natriuretic Peptide, Brain / biosynthesis*
  • Peptides / chemistry
  • Phosphorylation
  • Promoter Regions, Genetic
  • Protein Biosynthesis
  • Pyridines / pharmacology
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction
  • Time Factors
  • Transcription, Genetic
  • Transcriptional Activation
  • Transfection
  • Transplantation
  • Tumor Necrosis Factor-alpha / metabolism
  • Up-Regulation*
  • p38 Mitogen-Activated Protein Kinases / metabolism*

Substances

  • Culture Media, Conditioned
  • Cytokines
  • Imidazoles
  • Interleukin-1
  • Peptides
  • Pyridines
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Natriuretic Peptide, Brain
  • Interferon-gamma
  • p38 Mitogen-Activated Protein Kinases
  • SB 203580