Evidence map›Paper›PMID 21199871›Full record

ArticleThe Journal of biological chemistry2011

Inhibition of MAPK by prolactin signaling through the short form of its receptor in the ovary and decidua: involvement of a novel phosphatase.

Y Sangeeta Devi, Anita M Seibold, Aurora Shehu, Evelyn Maizels, Julia Halperin, Jamie Le, Nadine Binart, Lei Bao, Geula Gibori

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 21% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Systematic review of p38 mitogen-activated kinase and its functional role in reproductive tissues.American journal of reproductive immunology (New York, N.Y. : 1989) · 2018
    Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. The crucial role of prolactin-lactogenic hormone in Covid-19.Molecular and cellular biochemistry · 2022
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Mapping out p38MAPK.American journal of reproductive immunology (New York, N.Y. : 1989) · 2017
    Review
  15. Article
  16. Prolactin prevents hepatocellular carcinoma by restricting innate immune activation of c-Myc in mice.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  17. Article
  18. Article
  19. Article
  20. Article
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

9 authors at 2 institutions in 2 countries.

Y Sangeeta DeviDepartment of Physiology and Biophysics, University of Illinois at Chicago College of Medicine, Chicago, Illinois 60612, USA.
Anita M Seibold
Aurora Shehu
Evelyn Maizels
Julia Halperin
Jamie Le
Nadine Binart
Lei Bao
Geula Gibori
University of Illinois Chicago · USInserm · FR

Funding

TRAINING IN CELLULAR SIGNALLING IN THE CARDIOVASCULAR SYT32HL007692 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SOLARO, R JOHN · 1990 to 2014
$8.5M
REGULATION OF LUTEAL FUNCTION IN THE PREGNANT RATR01HD011119 · NICHD · UNIVERSITY OF ILLINOIS AT CHICAGO · PI GIBORI, GEULA · 1985 to 2009
$2.3M
FUNCTION OF THE DECIDUAL TISSUER01HD012356 · NICHD · UNIVERSITY OF ILLINOIS AT CHICAGO · PI GIBORI, GEULA · 1986 to 2007
$1.8M
REGULATION OF LUTEAL FUNCTIONR37HD011119 · NICHD · UNIVERSITY OF ILLINOIS AT CHICAGO · PI GIBORI, GEULA · 1988 to 1997
–
NHLBI NIH HHS T32 HL007692NICHD NIH HHS HD11119NICHD NIH HHS HD 12356NICHD NIH HHS R01 HD011119NICHD NIH HHS R01 HD012356NICHD NIH HHS R37 HD011119
6 · The paper itself

Abstract

Prolactin (PRL) is essential for normal reproduction and signals through two types of receptors, the short (PRL-RS) and long (PRL-RL) form. We have previously shown that transgenic mice expressing only PRL-RS (PRLR(-/-)RS) display abnormal follicular development and premature ovarian failure. Here, we report that MAPK, essential for normal follicular development, is critically inhibited by PRL in reproductive tissues of PRLR(-/-)RS mice. Consequently, the phosphorylation of MAPK downstream targets are also markedly inhibited by PRL without affecting immediate upstream kinases, suggesting involvement of MAPK specific phosphatase(s) in this inhibition. Similar results are obtained in a PRL-responsive ovary-derived cell line (GG-CL) that expresses only PRL-RS. However, we found the expression/activation of several known MAPK phosphatases not to be affected by PRL, suggesting a role of unidentified phosphatase(s). We detected a 27-kDa protein that binds to the intracellular domain of PRL-RS and identified it as dual specific phosphatase DUPD1. PRL does not induce expression of DUDP1 but represses its phosphorylation on Thr-155. We also show a physical association of this phosphatase with ERK1/2 and p38 MAPK. Using an in vitro phosphatase assay and overexpression studies, we established that DUPD1 is a MAPK phosphatase. Dual specific phosphatase inhibitors as well as siRNA to DUPD1, completely prevent PRL-mediated MAPK inhibition in ovarian cells. Our results strongly suggest that deactivation of MAPK by PRL/PRL-RS contributes to the severe ovarian defect in PRLR(-/-)RS mice and demonstrate the novel association of PRL-RS with DUPD1 and a role for this phosphatase in MAPK deactivation.

Indexed as

AnimalsCell LineDeciduaDual Specificity Phosphatase 1FemaleMAP Kinase Signaling SystemMiceMice, TransgenicMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Ovaryp38 Mitogen-Activated Protein KinasesPhosphoric Monoester HydrolasesPregnancyPrimary Ovarian InsufficiencyProlactinDual Specificity Phosphatase 1Dusp1 protein, mouseMapk1 protein, mouseMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3p38 Mitogen-Activated Protein KinasesPhosphoric Monoester HydrolasesProlactinReceptors, Prolactin

Identifiers

PMID21199871
PMCPMC3045015
OpenAlexW2050479720

What OpenQuestion holds

Textmetadata
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.