Literature DB >> 7588291

Hormonal regulation of messenger ribonucleic acid encoding steroidogenic acute regulatory protein in ovine corpora lutea.

J L Juengel1, B M Meberg, A M Turzillo, T M Nett, G D Niswender.   

Abstract

Steroidogenic acute regulatory protein (StAR), proposed to be involved in the transport of cholesterol to the inner mitochondrial membrane, has recently been cloned from MA-10 cells. Using reverse transcription-polymerase chain reaction, we generated a complementary DNA encoding 404 base pairs of StAR from ovine luteal tissue to perform studies regarding regulation of the messenger RNA (mRNA) encoding this protein. In Exp 1, ewes were hypophysectomized (HPX) on day 5 of the estrous cycle and administered saline or physiological regimens of LH and/or GH until collection of luteal tissue on day 12 of the estrous cycle (n = 4/group). Luteal concentrations [mean +/- SEM; femtomoles per microgram poly(A)+ RNA] of mRNA encoding StAR were lower (P < 0.05) in the HPX plus saline-treated ewes (26.4 +/- 7.3) than in day 12 pituitary-intact ewes (n = 4; 77.7 +/- 9.3). Replacement of LH (59.1 +/- 13.1), GH (59.1 +/- 12.8), or LH and GH (69.9 +/- 4.5) in HPX ewes increased (P < 0.05) concentrations of mRNA encoding StAR to values not different from those in day 12 controls. In Exp 2, ewes on day 11 or 12 of the estrous cycle were injected with prostaglandin F2 alpha (PGF2 alpha) to induce luteal regression. Corpora lutea were collected 4, 12, or 24 h after injection (n = 4-5/time point) and from untreated control ewes (n = 4) or 24 h after injection of saline (n = 4). Treatment with PGF2 alpha decreased (P < 0.05) concentrations of progesterone in serum 4, 12, and 24 h after injection. Concentrations of StAR mRNA were decreased (P < 0.01) to 47%, 19%, and 8% of control values 4, 12, and 24 h after PGF2 alpha injection, respectively. In Exp 3, ewes received ovarian arterial infusions of saline, PGF2 alpha, or phorbol 12-myristate 13-acetate (PMA), and luteal tissue was collected 0 (no infusion), 4, 12, or 24 h later (n = 3-4/group). Treatment with PGF2 alpha or PMA decreased (P < 0.05) concentrations of progesterone in serum 4, 12, and 24 h postinjection. Steady state concentrations of mRNA encoding StAR (P < 0.05) were 36% and 25% of the control value 12 and 24 h after PGF2 alpha injection. Injection of PMA decreased (P < 0.05) concentrations of StAR mRNA to 75% and 50% of control values at 4 and 12 h, but concentrations of mRNA encoding StAR were not different from control values at 24 h.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1995        PMID: 7588291     DOI: 10.1210/endo.136.12.7588291

Source DB:  PubMed          Journal:  Endocrinology        ISSN: 0013-7227            Impact factor:   4.736


  16 in total

Review 1.  The steroidogenic acute regulatory (StAR) protein two years later. An update.

Authors:  D M Stocco
Journal:  Endocrine       Date:  1997-04       Impact factor: 3.633

2.  Identification of a regulatory loop for the synthesis of neurosteroids: a steroidogenic acute regulatory protein-dependent mechanism involving hypothalamic-pituitary-gonadal axis receptors.

Authors:  Sivan Vadakkadath Meethal; Tianbing Liu; Hsien W Chan; Erika Ginsburg; Andrea C Wilson; Danielle N Gray; Richard L Bowen; Barbara K Vonderhaar; Craig S Atwood
Journal:  J Neurochem       Date:  2009-05-29       Impact factor: 5.372

3.  Effect of decreasing intraluteal progesterone on sensitivity of the early porcine corpus luteum to the luteolytic actions of prostaglandin F2alpha.

Authors:  Francisco J Diaz; Wenxiang Luo; Milo C Wiltbank
Journal:  Biol Reprod       Date:  2010-08-25       Impact factor: 4.285

4.  Prostaglandin F2α reduces steroidogenic acute regulatory (StAR) protein messenger ribonucleic acid expression in the rat ovary.

Authors:  T W Sandhoff; M P McLean
Journal:  Endocrine       Date:  1996-10       Impact factor: 3.633

5.  Convergence of 3',5'-cyclic adenosine 5'-monophosphate/protein kinase A and glycogen synthase kinase-3beta/beta-catenin signaling in corpus luteum progesterone synthesis.

Authors:  Lynn Roy; Claudia A McDonald; Chao Jiang; Dulce Maroni; Anthony J Zeleznik; Todd A Wyatt; Xiaoying Hou; John S Davis
Journal:  Endocrinology       Date:  2009-10-09       Impact factor: 4.736

6.  Growth hormone and gene expression of in vitro-matured rhesus macaque oocytes.

Authors:  Jenna K Nyholt de Prada; Lori D Kellam; Bela G Patel; Keith E Latham; Catherine A Vandevoort
Journal:  Mol Reprod Dev       Date:  2010-04       Impact factor: 2.609

7.  Upregulation of human chorionic gonadotrophin-induced steroidogenic acute regulatory protein by insulin-like growth factor-I in rat Leydig cells.

Authors:  T Lin; D Wang; J Hu; D M Stocco
Journal:  Endocrine       Date:  1998-02       Impact factor: 3.633

8.  Concentration of mRNA encoding 3 beta-hydroxysteroid dehydrogenase/delta 5,delta 4 isomerase (3 beta-HSD) and 3 beta-HSD enzyme activity following treatment of ewes with prostaglandin F2 alpha.

Authors:  J L Juengel; B M Meberg; E W McIntush; M F Smith; G D Niswender
Journal:  Endocrine       Date:  1998-02       Impact factor: 3.633

9.  Luteal expression of steroidogenic factor-1 mRNA during the estrous cycle and in response to luteotropic and luteolytic stimuli in ewes.

Authors:  J L Juengel; T L Larrick; B M Meberg; G D Niswender
Journal:  Endocrine       Date:  1998-12       Impact factor: 3.925

10.  Detection of hCG Responsive Expression of the Steroidogenic Acute Regulatory Protein in Mouse Leydig Cells.

Authors:  Pulak R. Manna; Ilpo T. Huhtaniemi; Douglas M. Stocco
Journal:  Biol Proced Online       Date:  2004-05-26       Impact factor: 3.244

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