Evidence map›Paper›PMID 39152497›Full record

ArticleBiological research2024

Placental growth factor mediates pathological uterine angiogenesis by activating the NFAT5-SGK1 signaling axis in the endometrium: implications for preeclampsia development.

Janet P Raja Xavier, Toshiyuki Okumura, Melina Apweiler, Nirzari A Chacko, Yogesh Singh, Sara Y Brucker, Satoru Takeda, Florian Lang, Madhuri S Salker

Abstract read
In one paragraph

Article in Biological research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Cells · 2026
    Article
  5. BPGM shapes NFAT5-driven cellular responses.Cellular and molecular life sciences : CMLS · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. 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

9 authors.

Janet P Raja XavierDepartment of Women's Health, University of Tübingen, 72076, Calwerstraße 7/6, Tübingen, Germany.
Toshiyuki OkumuraDepartment of Obstetrics and Gynaecology, Juntendo University School of Medicine, Tokyo, Japan.
Melina ApweilerDepartment of Women's Health, University of Tübingen, 72076, Calwerstraße 7/6, Tübingen, Germany.
Nirzari A ChackoDepartment of Women's Health, University of Tübingen, 72076, Calwerstraße 7/6, Tübingen, Germany.
Yogesh SinghDepartment of Women's Health, University of Tübingen, 72076, Calwerstraße 7/6, Tübingen, Germany.
Sara Y BruckerDepartment of Women's Health, University of Tübingen, 72076, Calwerstraße 7/6, Tübingen, Germany.
Satoru TakedaDepartment of Obstetrics and Gynaecology, Juntendo University School of Medicine, Tokyo, Japan.
Florian LangDepartment of Physiology, University of Tübingen, Tübingen, Germany.
Madhuri S SalkerDepartment of Women's Health, University of Tübingen, 72076, Calwerstraße 7/6, Tübingen, Germany. madhuri.salker@med.uni-tuebingen.de.ORCID http://orcid.org/0000-0002-7939-289X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

After menstruation the uterine spiral arteries are repaired through angiogenesis. This process is tightly regulated by the paracrine communication between endometrial stromal cells (EnSCs) and endothelial cells. Any molecular aberration in these processes can lead to complications in pregnancy including miscarriage or preeclampsia (PE). Placental growth factor (PlGF) is a known contributing factor for pathological angiogenesis but the mechanisms remain poorly understood. In this study, we investigated whether PlGF contributes to pathological uterine angiogenesis by disrupting EnSCs and endothelial paracrine communication. We observed that PlGF mediates a tonicity-independent activation of nuclear factor of activated T cells 5 (NFAT5) in EnSCs. NFAT5 activated downstream targets including SGK1, HIF-1α and VEGF-A. In depth characterization of PlGF - conditioned medium (CM) from EnSCs using mass spectrometry and ELISA methods revealed low VEGF-A and an abundance of extracellular matrix organization associated proteins. Secreted factors in PlGF-CM impeded normal angiogenic cues in endothelial cells (HUVECs) by downregulating Notch-VEGF signaling. Interestingly, PlGF-CM failed to support human placental (BeWo) cell invasion through HUVEC monolayer. Inhibition of SGK1 in EnSCs improved angiogenic effects in HUVECs and promoted BeWo invasion, revealing SGK1 as a key intermediate player modulating PlGF mediated anti-angiogenic signaling. Taken together, perturbed PlGF-NFAT5-SGK1 signaling in the endometrium can contribute to pathological uterine angiogenesis by negatively regulating EnSCs-endothelial crosstalk resulting in poor quality vessels in the uterine microenvironment. Taken together the signaling may impact on normal trophoblast invasion and thus placentation and, may be associated with an increased risk of complications such as PE.

Indexed as

EndometriumNeovascularization, PathologicPlacenta Growth FactorPre-EclampsiaProtein Serine-Threonine KinasesTranscription FactorsEnzyme-Linked Immunosorbent AssayFemaleHumansImmediate-Early ProteinsPregnancySerum-Glucocorticoid Regulated KinasesSignal TransductionStromal CellsImmediate-Early ProteinsNFAT5 protein, humanPlacenta Growth FactorProtein Serine-Threonine KinasesSerum-Glucocorticoid Regulated KinasesTranscription FactorsEndometriumPlacentationPlGFPreeclampsiaPregnancySGK1

Identifiers

PMID39152497
PMCPMC11330076

What Socratic holds

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LicenceCC BY
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 Socratic graph.