Glucocorticoids promote structural and functional maturation of foetal cardiomyocytes: A role for PGC-1α

E.A. Rog-Zielinska, M. A. Craig, J. R. Manning, R. V. Richardson, G. J. Gowans, D. R. Dunbar, K. Gharbi, C. J. Kenyon, M. C. Holmes, D. G. Hardie, G. L. Smith, K. E. Chapman

Research output: Contribution to journalArticlepeer-review

70 Citations (Scopus)


Glucocorticoid levels rise dramatically in late gestation to mature foetal organs in readiness for postnatal life. Immature heart function may compromise survival. Cardiomyocyte glucocorticoid receptor (GR) is required for the structural and functional maturation of the foetal heart in vivo, yet the molecular mechanisms are largely unknown. Here we asked if GR activation in foetal cardiomyocytes in vitro elicits similar maturational changes. We show that physiologically relevant glucocorticoid levels improve contractility of primary-mouse-foetal cardiomyocytes, promote Z-disc assembly and the appearance of mature myofibrils, and increase mitochondrial activity. Genes induced in vitro mimic those induced in vivo and include PGC-1α, a critical regulator of cardiac mitochondrial capacity. SiRNA-mediated abrogation of the glucocorticoid induction of PGC-1α in vitro abolished the effect of glucocorticoid on myofibril structure and mitochondrial oxygen consumption. Using RNA sequencing we identified a number of transcriptional regulators, including PGC-1α, induced as primary targets of GR in foetal cardiomyocytes. These data demonstrate that PGC-1α is a key mediator of glucocorticoid-induced maturation of foetal cardiomyocyte structure and identify other candidate transcriptional regulators that may play critical roles in the transition of the foetal to neonatal heart.

Original languageEnglish
Pages (from-to)1106-1116
Number of pages11
JournalCell Death and Differentiation
Issue number7
Publication statusPublished - 1 Jul 2015
Externally publishedYes


Dive into the research topics of 'Glucocorticoids promote structural and functional maturation of foetal cardiomyocytes: A role for PGC-1α'. Together they form a unique fingerprint.

Cite this