Effects of transforming growth factor-beta on human fetal adrenal steroid production.

Academic Article

Abstract

  • Transforming growth factor-beta (TGF-beta) was found to inhibit basal and ACTH-stimulated steroid production by cultured human fetal adrenal cells. The inhibitory effects of TGF-beta were both time and dose-dependent. Inhibition of basal dehydroepiandrosterone sulfate (DS) production usually was noted only after 3 or more days of treatment with > or = 0.1 ng TGF-beta/ml. The inhibitory effects of 1 ng/ml TGF-beta on ACTH-stimulated DS production were more striking than those on cortisol production by both fetal zone and neocortical cells. TGF-beta also was found to interfere with DS and cortisol production by fetal zone cells in response to forskolin and dibutyryl cAMP. TGF-beta interfered with ACTH stimulation of cytochrome P450(17) alpha mRNA in fetal zone and neocortex cells. These results are suggestive that TGF-beta differentially inhibits DS and cortisol production by human fetal adrenal cells and that the site of TGF-beta action on steroidogenesis may be distal to the generation of cAMP. Such results, along with those of others, are suggestive that TGF-beta may play an autocrine/paracrine role in the human adrenal.
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    Published In

    Keywords

  • Adenylyl Cyclases, Adrenal Cortex Hormones, Adrenal Glands, Adrenocorticotropic Hormone, Bucladesine, Cells, Cultured, Colforsin, Dehydroepiandrosterone, Dehydroepiandrosterone Sulfate, Humans, Hydrocortisone, RNA, Messenger, Steroid 17-alpha-Hydroxylase, Transforming Growth Factor beta
  • Digital Object Identifier (doi)

    Author List

  • Stankovic AK; Dion LD; Parker CR
  • Start Page

  • 145
  • End Page

  • 151
  • Volume

  • 99
  • Issue

  • 2