Literature DB >> 15087430

Pregnancy-associated plasma protein-a production in rat granulosa cells: stimulation by follicle-stimulating hormone and inhibition by the oocyte-derived bone morphogenetic protein-15.

Motozumi Matsui1, Barbara Sonntag, Seong Soo Hwang, Tara Byerly, Ariel Hourvitz, Eli Y Adashi, Shunichi Shimasaki, Gregory F Erickson.   

Abstract

Pregnancy-associated plasma protein-A (PAPP-A) is the major IGF binding protein-4 (IGFBP-4) protease in follicular fluid, consistent with its proposed role in folliculogenesis. Despite growing interest, almost nothing is known about how PAPP-A expression is regulated in any tissue. Here we show that FSH and oocytes regulate PAPP-A expression in granulosa cells (GCs). By in situ hybridization, ovary PAPP-A mRNA was markedly increased by pregnant mare serum gonadotropin treatment, and the message was localized to the membrana GCs but not cumulus GCs (CGCs) of dominant follicles. To explore the mechanism, we used primary cultures of rat GCs. Control (untreated) cells produced little or no PAPP-A spontaneously. Conversely, FSH markedly stimulated PAPP-A mRNA and protein in a dose- and time-dependent fashion. Interestingly, PAPP-A expression in isolated CGCs was also strongly induced by FSH, and the induction was inhibited by added oocytes. To investigate the nature of the inhibition, we tested the effect of oocyte-derived bone morphogenetic protein-15 (BMP-15). BMP-15 alone had no effect on basal levels of PAPP-A expression by cultures of membrana GCs or CGCs. However, BMP-15 markedly inhibited the FSH stimulation of PAPP-A production in a dose-dependent manner. The cleavage of IGFBP-4 by conditioned media from FSH-treated GCs was completely inhibited by anti-PAPP-A antibody, indicating the IGFBP-4 protease secreted by GCs is PAPP-A. These results demonstrate stimulatory and inhibitory roles for FSH and BMP-15, respectively, in regulating PAPP-A production by GCs. We propose that FSH and oocyte-derived BMP-15 form a controlling network that ensures the spatiotemporal pattern of GC PAPP-A expression in the dominant follicle.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15087430     DOI: 10.1210/en.2003-1642

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


  6 in total

1.  Lack of functional pregnancy-associated plasma protein-A (PAPPA) compromises mouse ovarian steroidogenesis and female fertility.

Authors:  Mette Nyegaard; Michael T Overgaard; You-Qiang Su; Amy E Hamilton; Jakub Kwintkiewicz; Minnie Hsieh; Nihar R Nayak; Marco Conti; Cheryl A Conover; Linda C Giudice
Journal:  Biol Reprod       Date:  2010-02-03       Impact factor: 4.285

2.  Fetal and neonatal exposure to the endocrine disruptor methoxychlor causes epigenetic alterations in adult ovarian genes.

Authors:  Aparna Mahakali Zama; Mehmet Uzumcu
Journal:  Endocrinology       Date:  2009-07-09       Impact factor: 4.736

3.  Oocyte-specific overexpression of mouse bone morphogenetic protein-15 leads to accelerated folliculogenesis and an early onset of acyclicity in transgenic mice.

Authors:  Heather E McMahon; Osamu Hashimoto; Pamela L Mellon; Shunichi Shimasaki
Journal:  Endocrinology       Date:  2008-02-28       Impact factor: 4.736

4.  Computational modelling of bovine ovarian follicle development.

Authors:  Dagmar Iber; Christian De Geyter
Journal:  BMC Syst Biol       Date:  2013-07-15

Review 5.  Insulin-Like Growth Factor Binding Proteins and IGFBP Proteases: A Dynamic System Regulating the Ovarian Folliculogenesis.

Authors:  Sabine Mazerbourg; Philippe Monget
Journal:  Front Endocrinol (Lausanne)       Date:  2018-03-29       Impact factor: 5.555

6.  Celastrol Prevents Oxidative Stress Effects on FSHR, PAPP, and CYP19A1 Gene Expression in Cultured Human Granulosa-Lutein Cells.

Authors:  Rita Martín-Ramírez; Rebeca González-Fernández; Deborah Rotoli; Jairo Hernández; Pablo Martín-Vasallo; Angela Palumbo; Julio Ávila
Journal:  Int J Mol Sci       Date:  2021-03-30       Impact factor: 5.923

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.