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PMID: 14715710 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Molten globule structure and steroidogenic activity of N-218 MLN64 in human placental mitochondria.

Endocrinology ·Vol. 145 ·No. 4 ·2004-04-00 ·Pages 1700-7

Tuckey RC, Bose HS, Czerwionka I, Miller WL

Abstract

Progesterone synthesis by the human placenta requires the conversion of mitochondrial cholesterol to pregnenolone by cytochrome P450scc. Most steroidogenic tissues use the steroidogenic acute regulatory protein (StAR) to deliver cholesterol to the inner mitochondrial membrane where P450scc is located, but StAR is not expressed in the human placenta. However, the human placenta does express MLN64, which has a C-terminal domain homologous to StAR that can also transport cholesterol. We investigated the ability of bacterially expressed N-218 MLN64 and N-62 StAR to transport cholesterol between artificial membranes and to its inner membrane site of use in placental mitochondria. Urea denaturation experiments show that N-218 MLN64 undergoes a pH-dependent and denaturant-dependent structural transition to a molten globule state, as reported previously for N-62 StAR. N-218 MLN64 stimulated cholesterol transfer between artificial phospholipid vesicles with an initial rate of 6.5 mol/min.mol N-218 MLN64. Both N-218 MLN64 and N-62 StAR stimulated cholesterol transfer to the inner mitochondrial membrane, as evidenced by a 6-fold stimulation of pregnenolone synthesis with saturating transporter. This stimulation was seen only after the endogenous cholesterol in the steroidogenic pool of the isolated mitochondria was first depleted. No stimulation was observed by N-218 MLN64 or N-62 StAR when 20alpha-hydroxycholesterol was added as substrate for P450scc, confirming that these proteins stimulate P450scc activity by enhancing cholesterol transport. MLN64 levels in placental JEG-3 cells were unresponsive to stimulation by 8-bromo-cAMP over 24 h. These data show that human N-218 MLN64 and N-62 StAR have similar biophysical and functional properties and are able to stimulate steroidogenesis in a human placental system, which normally lacks StAR. The results reveal that with saturating MLN64, steroidogenesis by placental mitochondria proceeds at near-maximal rate.

MeSH Terms
8-Bromo Cyclic Adenosine Monophosphate/pharmacology Biological Transport Cell Line Cholesterol/metabolism Female Humans Membrane Proteins/chemistry,drug effects,pharmacology,physiology Mitochondria/metabolism Phosphoproteins/pharmacology Placenta/metabolism Pregnenolone/biosynthesis Protein Denaturation Urea/pharmacology
Chemicals
Membrane Proteins Phosphoproteins STARD3NL protein, human steroidogenic acute regulatory protein 8-Bromo Cyclic Adenosine Monophosphate Pregnenolone Urea Cholesterol
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Tuckey Robert C
Department of Biochemistry and Molecular Biology, School of Biomedical and Chemical Sciences, The University of Western Australia, Crawley, Australia. [email protected]
Bose Himangshu S
Czerwionka Inez
Miller Walter L
Article Info
Journal
Endocrinology
Abbr.
Endocrinology
ISSN
0013-7227
Published
2004-04-00
Epub
2004-00-08
Pages
1700-7
Language
English
Region
United States
NLM ID
0375040
Subset
IM
Grants
NIDDK NIH HHS · DK02762 · United States
NIDDK NIH HHS · DK37922 · United States
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