Contribution of apoptosis to the phenotypic changes of adrenocortical cells in primary culture

Mol Cell Endocrinol. 1995 Apr 28;110(1-2):175-84. doi: 10.1016/0303-7207(95)03530-k.

Abstract

The aim of this study was to evaluate the occurrence and physiological consequences of apoptosis in primary cultures of bovine adrenocortical cells (of fasciculata-reticularis origin). Under ACTH-free culture conditions, we observed apoptotic cells in the cell layer and the accumulation of apoptotic bodies in the culture medium. These were hardly detectable in ACTH-supplemented cultures. Under ACTH-free conditions, the DNA content of apoptotic bodies collected over 48 h represented up to 10-15% of that of the cell layer at the onset of the culture (as compared to 3% in ACTH-supplemented cultures). Past the fourth day of culture in the absence of ACTh, most cells lacked several markers of their originating fasciculata-reticularis phenotype and progressively evolved to an undifferentiated phenotype. The vast majority of the apoptotic bodies released during the first 4 days of culture were immunoreactive for P450 17 alpha. Inversely, during the same period of time, the proliferating cells (PCNA-positive) did not appear to express P450 17 alpha. Therefore, apoptosis could contribute, together with dedifferentiation, to the phenotype shift observed in ACTH-depleted cultures of adrenal fasciculata-reticularis cells. These observations also characterize this endocrine cell system as an in vitro model for the study of hormone-repressed apoptosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenal Cortex / cytology*
  • Adrenal Cortex / drug effects
  • Adrenal Cortex / metabolism
  • Adrenocorticotropic Hormone / administration & dosage
  • Adrenocorticotropic Hormone / pharmacology
  • Animals
  • Apoptosis*
  • Cattle
  • Cell Count
  • Cell Differentiation
  • Cells, Cultured
  • Chromatin / ultrastructure
  • Cytochrome P-450 CYP11B2
  • Cytochrome P-450 Enzyme System / metabolism
  • DNA / metabolism
  • Microscopy, Electron
  • Phenotype
  • Steroid 11-beta-Hydroxylase / metabolism

Substances

  • Chromatin
  • Adrenocorticotropic Hormone
  • DNA
  • Cytochrome P-450 Enzyme System
  • Cytochrome P-450 CYP11B2
  • Steroid 11-beta-Hydroxylase