Abstract |
Apoptosis inhibits steroid biosynthesis, but it is not clear how the Steroidogenic Acute Regulatory (StAR) protein, is affected. To characterize StAR expression during apoptosis, mouse MA-10 Leydig tumor cells were treated with ethane dimethane sulfonate (EDS), an inducer of apoptosis, and the metal ion chelator NNN'N'-tetrakis-(2-pyridylmethyl)ethylenediamine ( TPEN), an inducer of cell death. Both chemicals induced cell death and similarly inhibited dbcAMP-stimulated steroidogenesis and accumulation of the 30 kDa form of StAR. Utilizing the dye JC-1, it was found that TPEN and EDS also impaired the mitochondrial electrochemical potential (delta psi). In Sertoli cells, which also express StAR, EDS induced cell death and attenuated StAR expression. We conclude 1) steroidogenesis and accumulation of mature StAR protein are inhibited as a consequence of the induction of apoptosis; 2) reduced levels of StAR may be partially attributed to inhibition of import because of the loss of delta psi; 3) loss of steroidogenesis is probably due to loss of StAR synthesis and disruption of delta psi.
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Authors | S R King, F F Rommerts, S L Ford, J C Hutson, J Orly, D M Stocco |
Journal | Endocrine research
(Endocr Res)
1998 Aug-Nov
Vol. 24
Issue 3-4
Pg. 469-78
ISSN: 0743-5800 [Print] England |
PMID | 9888527
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Ethylenediamines
- Mesylates
- Phosphoproteins
- Steroids
- steroidogenic acute regulatory protein
- ethylene dimethanesulfonate
- N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine
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Topics |
- Animals
- Cell Line
- Electrochemistry
- Ethylenediamines
(pharmacology)
- Leydig Cells
(drug effects, metabolism)
- Male
- Mesylates
(pharmacology)
- Mice
- Mitochondria
(drug effects, physiology)
- Phosphoproteins
(antagonists & inhibitors, metabolism)
- Rats
- Rats, Sprague-Dawley
- Sertoli Cells
(drug effects, metabolism)
- Steroids
(biosynthesis)
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