Evidence map›Paper›PMID 37942801›Full record

ArticleEndocrinology2023

Classical Estrogen Signaling in Ciliated Epithelial Cells of the Oviduct Is Nonessential for Fertility in Female Mice.

Emily A McGlade, Kalli K Stephens, Sarayut Winuthayanon, Prashanth Anamthathmakula, Michael J Holtzman, Wipawee Winuthayanon

Open access · greenAbstract read
In one paragraph

Article in Endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Hormonal regulation of cilia in the female reproductive tract.Current opinion in endocrine and metabolic research · 2024
    Article
  6. Cilia Structure and Function in Human Disease.Current opinion in endocrine and metabolic research · 2024
    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

6 authors at 4 institutions in 1 country.

Emily A McGladeObstetrics, Gynecology and Women's Health, School of Medicine, University of Missouri, Columbia, MO 65211, USA.ORCID 0000-0003-4979-9979
Kalli K StephensObstetrics, Gynecology and Women's Health, School of Medicine, University of Missouri, Columbia, MO 65211, USA.
Sarayut WinuthayanonDivision of Animal Sciences, University of Missouri, Columbia, MO 65211, USA.ORCID 0000-0002-8439-0389
Prashanth AnamthathmakulaSchool of Medicine, University of Missouri-Kansas City, Kansas City, MO 64108, USA.ORCID 0000-0002-0664-9746
Michael J HoltzmanPulmonary and Critical Care Medicine, Department of Medicine, Washington University School of Medicine, St.Louis, MO 63110, USA.ORCID 0000-0001-8750-3716
Wipawee WinuthayanonObstetrics, Gynecology and Women's Health, School of Medicine, University of Missouri, Columbia, MO 65211, USA.ORCID 0000-0002-5196-8471
University of Missouri Health System · USUniversity of Missouri · USUniversity of Missouri–Kansas City · USWashington University in St. Louis · US

Funding

Defining and Controlling Airway DiseaseR35HL145242 · NHLBI · WASHINGTON UNIVERSITY · PI HOLTZMAN, MICHAEL J · 2019 to 2025
$6.6M
The actions of steroid hormones on oviduct functionR01HD097087 · NICHD · WASHINGTON STATE UNIVERSITY · PI WINUTHAYANON, WIPAWEE · 2019 to 2023
$1.7M
MARC at Washington State UniversityT34GM141971 · NIGMS · WASHINGTON STATE UNIVERSITY · PI GIZERIAN, SAMANTHA, KOSTYUKOVA, ALLA S. · 2021 to 2025
$1.3M
The Role of Progesterone Receptor in the Oviduct Epithelium for Pregnancy EstablishmentF31HD107807 · NICHD · WASHINGTON STATE UNIVERSITY · PI MCGLADE, EMILY A · 2021 to 2021
$28k
NHLBI NIH HHS R35 HL145242NHLBI NIH HHS R35HL145242NICHD NIH HHS F31 HD107807NICHD NIH HHS R01 HD097087NIGMS NIH HHS T34 GM141971
6 · The paper itself

Abstract

Ciliary action performs a critical role in the oviduct (Fallopian tube) during pregnancy establishment through sperm and egg transport. The disruption of normal ciliary function in the oviduct affects oocyte pick-up and is a contributing factor to female infertility. Estrogen is an important regulator of ciliary action in the oviduct and promotes ciliogenesis in several species. Global loss of estrogen receptor α (ESR1) leads to infertility. We have previously shown that ESR1 in the oviductal epithelial cell layer is required for female fertility. Here, we assessed the role of estrogen on transcriptional regulation of ciliated epithelial cells of the oviduct using single-cell RNA-sequencing analysis. We observed minor variations in ciliated cell genes in the proximal region (isthmus and uterotubal junction) of the oviduct. However, 17β-estradiol treatment had little impact on the gene expression profile of ciliated epithelial cells. We also conditionally ablated Esr1 from ciliated epithelial cells of the oviduct (called ciliated Esr1d/d mice). Our studies showed that ciliated Esr1d/d females had fertility rates comparable to control females, did not display any disruptions in preimplantation embryo development or embryo transport to the uterus, and had comparable cilia formation to control females. However, we observed some incomplete deletion of Esr1 in the ciliated epithelial cells, especially in the ampulla region. Nevertheless, our data suggest that ESR1 expression in ciliated cells of the oviduct is dispensable for ciliogenesis and nonessential for female fertility in mice.

Indexed as

Fallopian TubesInfertility, FemaleAnimalsEpithelial CellsEstrogensFemaleFertilityHumansMaleMiceOviductsPregnancySemenEstrogensciliaepitheliumestrogenestrogen receptorfertilityoviductscRNA-seq

Identifiers

PMID37942801
PMCPMC10658216
OpenAlexW4388515835

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.