Endocrine Connections (Sep 2017)

Transcription controls growth, cell kinetics and cholesterol supply to sustain ACTH responses

  • Robert I Menzies,
  • Xin Zhao,
  • Linda J Mullins,
  • John J Mullins,
  • Carolynn Cairns,
  • Nicola Wrobel,
  • Donald R Dunbar,
  • Matthew A Bailey,
  • Christopher J Kenyon

DOI
https://doi.org/10.1530/EC-17-0092
Journal volume & issue
Vol. 6, no. 7
pp. 446 – 457

Abstract

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Chronic ACTH exposure is associated with adrenal hypertrophy and steroidogenesis. The underlying molecular processes in mice have been analysed by microarray, histological and immunohistochemical techniques. Synacthen infused for 2 weeks markedly increased adrenal mass and plasma corticosterone levels. Microarray analysis found greater than 2-fold changes in expression of 928 genes (P 4-fold and cross-sectional area of fasciculata cells was 2-fold greater. In contrast, genes associated with apoptosis (eg Casp12, Clu,) were downregulated and apoptotic cells (Tunel staining) were fewer (P < 0.001) and more widely distributed throughout the cortex. In summary, long-term steroidogenesis with ACTH excess is sustained by genes controlling cholesterol supply and adrenal mass. ACTH effects on adrenal morphology and genes controlling cell hypertrophy, proliferation and apoptosis suggest the involvement of different cell types and separate molecular pathways.

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