Evidence map›Paper›PMID 27009040›Full record

ArticleBiology of reproduction2016

Luteinizing Hormone Causes Phosphorylation and Activation of the cGMP Phosphodiesterase PDE5 in Rat Ovarian Follicles, Contributing, Together with PDE1 Activity, to the Resumption of Meiosis.

Jeremy R Egbert, Tracy F Uliasz, Leia C Shuhaibar, Andreas Geerts, Frank Wunder, Robin J Kleiman, John M Humphrey, Paul D Lampe, Nikolai O Artemyev, Sergei D Rybalkin and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Biology of reproduction, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
6.4field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
  2. Folliculogenesis: A Cellular Crosstalk Mechanism.Current issues in molecular biology · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Regulation of oocyte maturation: Role of conserved ERK signaling.Molecular reproduction and development · 2022
    Review
  11. Article
  12. Article
  13. Mechanisms of Oocyte Maturation and Related Epigenetic Regulation.Frontiers in cell and developmental biology · 2021
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. The art of oocyte meiotic arrest regulation.Reproductive biology and endocrinology : RB&E · 2019
    Review
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 8 institutions in 2 countries.

Jeremy R EgbertDepartment of Cell Biology, University of Connecticut Health Center, Farmington, Connecticut egbert@uchc.edu.
Tracy F UliaszDepartment of Cell Biology, University of Connecticut Health Center, Farmington, Connecticut.
Leia C ShuhaibarDepartment of Cell Biology, University of Connecticut Health Center, Farmington, Connecticut.
Andreas GeertsBayer Pharma AG, Pharma Research Center, Wuppertal, Germany.
Frank WunderBayer Pharma AG, Pharma Research Center, Wuppertal, Germany.
Robin J KleimanTranslational Neuroscience Center, Boston Children's Hospital, Boston, Massachusetts.
John M HumphreyPfizer Worldwide Research & Development, Groton, Connecticut.
Paul D LampeTranslational Research Program, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Nikolai O ArtemyevDepartment of Molecular Physiology and Biophysics, University of Iowa, Iowa City, Iowa.
Sergei D RybalkinDepartment of Pharmacology, University of Washington, Seattle, Washington.
Joseph A BeavoDepartment of Pharmacology, University of Washington, Seattle, Washington.
Matthew A MovsesianCardiology Section, VA Salt Lake City Health Care System and Division of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah.
Laurinda A JaffeDepartment of Cell Biology, University of Connecticut Health Center, Farmington, Connecticut ljaffe@uchc.edu.
UConn Health · USBayer (Germany) · DEUniversity of Washington · USBoston Children's Hospital · USFred Hutch Cancer Center · USPfizer (United States) · USUniversity of Iowa · USUniversity of Utah · US

Funding

PHOSPHORYLATION OF GAP JUNCTION PROTEINSR01GM055632 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LAMPE, PAUL D. · 1997 to 2017
$6.1M
Signal Transduction at FertilizationR37HD014939 · NICHD · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI JAFFE, LAURINDA A. · 2014 to 2023
$4.8M
Regulation of Cellular Functions by Cyclic Nucleotide Phosphodiesterase 8R01GM083926 · NIGMS · UNIVERSITY OF WASHINGTON · PI BEAVO, JOSEPH A · 2008 to 2015
$3.0M
NICHD NIH HHS R37 HD014939NIGMS NIH HHS R01 GM055632NIGMS NIH HHS R01 GM083926
6 · The paper itself

Abstract

The meiotic cell cycle of mammalian oocytes in preovulatory follicles is held in prophase arrest by diffusion of cGMP from the surrounding granulosa cells into the oocyte. Luteinizing hormone (LH) then releases meiotic arrest by lowering cGMP in the granulosa cells. The LH-induced reduction of cGMP is caused in part by a decrease in guanylyl cyclase activity, but the observation that the cGMP phosphodiesterase PDE5 is phosphorylated during LH signaling suggests that an increase in PDE5 activity could also contribute. To investigate this idea, we measured cGMP-hydrolytic activity in rat ovarian follicles. Basal activity was due primarily to PDE1A and PDE5, and LH increased PDE5 activity. The increase in PDE5 activity was accompanied by phosphorylation of PDE5 at serine 92, a protein kinase A/G consensus site. Both the phosphorylation and the increase in activity were promoted by elevating cAMP and opposed by inhibiting protein kinase A, supporting the hypothesis that LH activates PDE5 by stimulating its phosphorylation by protein kinase A. Inhibition of PDE5 activity partially suppressed LH-induced meiotic resumption as indicated by nuclear envelope breakdown, but inhibition of both PDE5 and PDE1 activities was needed to completely inhibit this response. These results show that activities of both PDE5 and PDE1 contribute to the LH-induced resumption of meiosis in rat oocytes, and that phosphorylation and activation of PDE5 is a regulatory mechanism.

Indexed as

AnimalsCells, CulturedCyclic GMPCyclic Nucleotide Phosphodiesterases, Type 1Cyclic Nucleotide Phosphodiesterases, Type 5FemaleLuteinizing HormoneMeiosisMiceMice, Inbred C57BLOocytesOvarian FolliclePhosphorylationRatsRats, Sprague-DawleyCyclic GMPCyclic Nucleotide Phosphodiesterases, Type 1Cyclic Nucleotide Phosphodiesterases, Type 5Luteinizing HormonePde5a protein, ratcyclic GMPcyclic nucleotide phosphodiesteraseluteinizing hormonemeiosisovarian follicle

Identifiers

PMID27009040
PMCPMC4939740
OpenAlexW2302705852

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.