Evidence map›Paper›PMID 32772088›Full record

ArticleThe Journal of clinical endocrinology and metabolism2020

Sexually Dimorphic Crosstalk at the Maternal-Fetal Interface.

Tianyanxin Sun, Tania L Gonzalez, Nan Deng, Rosemarie DiPentino, Ekaterina L Clark, Bora Lee, Jie Tang, Yizhou Wang, Barry R Stripp, Changfu Yao and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
4.8field-weighted citation impact, top 4% 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

47 citing papers in PubMed, 1 synthesis or guideline pooled it, 82 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 4 institutions in 1 country.

Tianyanxin SunDivision of Reproductive Endocrinology and Infertility; Department of Obstetrics and Gynecology, Cedars-Sinai Medical Center, Los Angeles, California.
Tania L GonzalezDivision of Reproductive Endocrinology and Infertility; Department of Obstetrics and Gynecology, Cedars-Sinai Medical Center, Los Angeles, California.
Nan DengBiostatistics and Bioinformatics Research Center, Cedars-Sinai Medical Center, Los Angeles, California.
Rosemarie DiPentinoDivision of Reproductive Endocrinology and Infertility; Department of Obstetrics and Gynecology, Cedars-Sinai Medical Center, Los Angeles, California.
Ekaterina L ClarkUniversity of California Los Angeles, Los Angeles, California.
Bora LeeDivision of Reproductive Endocrinology and Infertility; Department of Obstetrics and Gynecology, Cedars-Sinai Medical Center, Los Angeles, California.
Jie TangDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, California.
Yizhou WangDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, California.
Barry R StrippDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, California.
Changfu YaoDepartment of Medicine, Cedars-Sinai Medical Center, Los Angeles, California.
Hsian-Rong TsengCalifornia NanoSystems Institute, Department of Molecular and Medical Pharmacology, University of California, Los Angeles, California.
S Ananth KarumanchiDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, California.
Alexander F KoeppelCenter for Public Health Genomics, University of Virginia, Charlottesville, Virginia.
Stephen D TurnerCenter for Public Health Genomics, University of Virginia, Charlottesville, Virginia.
Charles R FarberCenter for Public Health Genomics, University of Virginia, Charlottesville, Virginia.
Stephen S RichCenter for Public Health Genomics, University of Virginia, Charlottesville, Virginia.
Erica T WangDivision of Reproductive Endocrinology and Infertility; Department of Obstetrics and Gynecology, Cedars-Sinai Medical Center, Los Angeles, California.
John WilliamsDivision of Reproductive Endocrinology and Infertility; Department of Obstetrics and Gynecology, Cedars-Sinai Medical Center, Los Angeles, California.
Margareta D PisarskaDivision of Reproductive Endocrinology and Infertility; Department of Obstetrics and Gynecology, Cedars-Sinai Medical Center, Los Angeles, California.
Cedars-Sinai Medical Center · USUniversity of Virginia · USCalifornia NanoSystems Institute · USUniversity of California, Los Angeles · US

Funding

Non-Invasive Prenatal Diagnostics Based on Circulating TrophoblastsU01EB026421 · NIBIB · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PISARSKA, MARGARETA, TSENG, HSIAN-RONG · 2019 to 2023
$4.0M
Effects of fetal sex on the first trimester transcriptomeR01HD074368 · NICHD · CEDARS-SINAI MEDICAL CENTER · PI PISARSKA, MARGARETA · 2013 to 2018
$3.4M
Training Program in Endocrinology, Diabetes, and MetabolismT32DK007770 · NIDDK · CEDARS-SINAI MEDICAL CENTER · PI MELMED, SHLOMO · 1999 to 2022
$3.4M
Noncoding RNA regulation of the human placental transcriptome among the sexesR01HD091773 · NICHD · CEDARS-SINAI MEDICAL CENTER · PI PISARSKA, MARGARETA · 2017 to 2018
$900k
NIBIB NIH HHS U01 EB026421NICHD NIH HHS R01 HD074368NICHD NIH HHS R01 HD091773NIDDK NIH HHS T32 DK007770
6 · The paper itself

Abstract

contextCrosstalk through receptor ligand interactions at the maternal-fetal interface is impacted by fetal sex. This affects placentation in the first trimester and differences in outcomes. Sexually dimorphic signaling at early stages of placentation are not defined.

objectiveInvestigate the impact of fetal sex on maternal-fetal crosstalk.

designReceptors/ligands at the maternal-fetal surface were identified from sexually dimorphic genes between fetal sexes in the first trimester placenta and defined in each cell type using single-cell RNA-Sequencing (scRNA-Seq).

settingAcademic institution. SAMPLES: Late first trimester (~10-13 weeks) placenta (fetal) and decidua (maternal) from uncomplicated ongoing pregnancies.

main outcome measuresTranscriptomic profiling at tissue and single-cell level; immunohistochemistry of select proteins.

resultsWe identified 91 sexually dimorphic receptor-ligand pairs across the maternal-fetal interface. We examined fetal sex differences in 5 major cell types (trophoblasts, stromal cells, Hofbauer cells, antigen-presenting cells, and endothelial cells). Ligands from the CC family chemokine ligand (CCL) family were most highly representative in females, with their receptors present on the maternal surface. Sexually dimorphic trophoblast transcripts, Mucin-15 (MUC15) and notum, palmitoleoyl-protein carboxylesterase (NOTUM) were also most highly expressed in syncytiotrophoblasts and extra-villous trophoblasts respectively. Gene Ontology (GO) analysis using sexually dimorphic genes in individual cell types identified cytokine mediated signaling pathways to be most representative in female trophoblasts. Upstream analysis demonstrated TGFB1 and estradiol to affect all cell types, but dihydrotestosterone, produced by the male fetus, was an upstream regulator most significant for the trophoblast population.

conclusionsMaternal-fetal crosstalk exhibits sexual dimorphism during placentation early in gestation.

Indexed as

Sex CharacteristicsDeciduaFemaleHumansMaternal-Fetal ExchangePlacentaPregnancyPregnancy Trimester, FirstReceptor Cross-TalkSequence Analysis, RNATranscriptomeTrophoblastsfirst trimester placentahuman pregnancyplacenta cell typesreceptor-ligandsex differencessingle-cell RNA sequencing

Identifiers

PMID32772088
PMCPMC7571453
OpenAlexW3047898585

What OpenQuestion holds

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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.