Evidence map›Paper›PMID 31814178›Full record

ArticleAmerican journal of reproductive immunology (New York, N.Y. : 1989)2020

Changes in mediators of pro-cell growth, senescence, and inflammation during murine gestation.

Narmada Lavu, Samantha Sheller-Miller, Talar Kechichian, Samir Cayenne, Elizabeth A Bonney, Ramkumar Menon

Open access · greenAbstract read
In one paragraph

Article in American journal of reproductive immunology (New York, N.Y. : 1989), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-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

7 citing papers in PubMed, 9 citations in OpenAlex.

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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

6 authors at 3 institutions in 1 country.

Narmada LavuDivision of Maternal-Fetal Medicine & Perinatal Research, Department of Obstetrics & Gynecology, The University of Texas Medical Branch at Galveston, Galveston, TX, USA.
Samantha Sheller-MillerDivision of Maternal-Fetal Medicine & Perinatal Research, Department of Obstetrics & Gynecology, The University of Texas Medical Branch at Galveston, Galveston, TX, USA.ORCID 0000-0002-3991-1747
Talar KechichianDivision of Maternal-Fetal Medicine & Perinatal Research, Department of Obstetrics & Gynecology, The University of Texas Medical Branch at Galveston, Galveston, TX, USA.
Samir CayenneUniversity of Texas at Austin, Austin, TX, USA.
Elizabeth A BonneyDepartment of Obstetrics and Gynecology, University of Vermont, Burlington, VT, USA.
Ramkumar MenonDivision of Maternal-Fetal Medicine & Perinatal Research, Department of Obstetrics & Gynecology, The University of Texas Medical Branch at Galveston, Galveston, TX, USA.ORCID 0000-0001-9213-6105
The University of Texas Medical Branch at Galveston · USThe University of Texas at Austin · USUniversity of Vermont · US

Funding

Fetal Membranes: An In-Vivo Model for Developmental Senescence and its ConsequencesR21AG060356 · NIA · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI BONNEY, ELIZABETH A., MENON, RAMKUMAR · 2018 to 2019
$445k
ROS-Induced p38 MAPK activation: A Novel Pathway to Preterm BirthR03HD086354 · NICHD · UNIVERSITY OF TEXAS MED BR GALVESTON · PI MENON, RAMKUMAR · 2016 to 2017
$155k
NIA NIH HHS R21 AG060356NICHD NIH HHS R03 HD086354
6 · The paper itself

Abstract

problemSenescence of the fetal membranes and senescence-associated inflammation have been associated with parturition at term and pre-term in both mice and humans. Using a pregnant mouse model, we determined changes in multiple molecular signalers contributing to senescence and inflammation associated with parturition. METHOD OF STUDY: Fetal membranes were collected from timed-pregnant CD-1 mice on gestation days (E) 13, 15, 17, 18, and 19. Immunohistochemistry (IHC) localized pro-cell growth factors glycogen synthase kinase 3β (GSK3β) and β-catenin. Gestational age-associated changes in pro-cell growth vs senescence mediators (p38 mitogen-activated protein kinase [p38MAPK]), prooxidants (heme oxygenase-1 [HO-1], peroxisome proliferator-activated receptor γ [PPARγ]), and pro- and anti-inflammatory cytokines (IL-6, IL-8, IL-10, and IL-1β) were determined by Western blots and Luminex assays.

resultsFetal membrane expressions of phosphorylated forms of GSK3β (inactivation) and p38MAPK (activation) increased, while β-catenin expression decreased, as gestation progressed. Antioxidant HO-1 expression decreased while PPARγ increased toward term gestation. IL-6 and IL-8 concentrations were highest on E19 (day of delivery), while IL-10 and IL-1β concentrations were highest on E15.

conclusionMouse fetal membranes showed a progressive senescence marker increase coincided with downregulation of cell growth factors. Development of senescence is associated with inflammation. Senescence-associated changes are natural and physiologic and indicative of fetal membranes' readiness for parturition.

Indexed as

PregnancyAnimalsbeta CateninCell Growth ProcessesCells, CulturedCellular SenescenceExtraembryonic MembranesFemaleGlycogen Synthase Kinase 3 betaInflammationMiceOxidative Stressp38 Mitogen-Activated Protein KinasesParturitionPPAR gammabeta CateninGlycogen Synthase Kinase 3 betap38 Mitogen-Activated Protein KinasesPPAR gammafetal membranesGSK3βoxidative stressp38MAPKpre-term laborsenescence

Identifiers

PMID31814178
PMCPMC7023982
OpenAlexW2995437125

What OpenQuestion holds

Textmetadata
LicenceTDM
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.