Nongenomic action of an insect steroid hormone in steroid-induced programmed cell death

Mol Cell Endocrinol. 2007 Jan 15;263(1-2):18-28. doi: 10.1016/j.mce.2006.08.005. Epub 2006 Oct 11.

Abstract

Programmed cell death (PCD) of the silkworm silk glands is triggered by the insect steroid hormone, 20-hydroxyecdysone (20E), and proceeds sequentially through cell shrinkage, nuclear condensation, DNA fragmentation, nuclear fragmentation and apoptotic body formation. A protein synthesis inhibitor, cycloheximide (CHX, 2 mM) induced a cell death that exhibited only nuclear and DNA fragmentation. A concentration of 0.2 mM CHX was ineffective at inducing the cell death when added alone, but in the presence of 20E, a cell death similar to that induced by 2 mM CHX was resulted with accompanying nuclear condensation. Since 2 and 0.2 mM CHX inhibited protein synthesis equally, the DNA and nuclear fragmentation appear to be mediated by a nongenomic action of 20E. In addition, we show a possible involvement of Ca2+-PKC-caspase-3 like protease pathway in the nongenomic action. The data suggest that 20E-induced PCD is accomplished through the integration of genomic and nongenomic actions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Apoptosis / genetics
  • Bombyx*
  • Calcium / metabolism
  • Caspase 3 / metabolism
  • Caspase Inhibitors
  • Cells, Cultured / cytology
  • Cells, Cultured / drug effects
  • Cycloheximide / pharmacology
  • Cysteine Proteinase Inhibitors / pharmacology
  • DNA / genetics
  • DNA / metabolism
  • Ecdysterone / pharmacology*
  • Larva / cytology
  • Protein Kinase C / antagonists & inhibitors
  • Protein Kinase C / metabolism

Substances

  • Caspase Inhibitors
  • Cysteine Proteinase Inhibitors
  • Ecdysterone
  • DNA
  • Cycloheximide
  • Protein Kinase C
  • Caspase 3
  • Calcium