Evidence map›Paper›PMID 31125045›Full record

ArticleEndocrinology2019

Msx Homeobox Genes Act Downstream of BMP2 to Regulate Endometrial Decidualization in Mice and in Humans.

Shanmugasundaram Nallasamy, Hatice S Kaya Okur, Arpita Bhurke, Juanmahel Davila, Quanxi Li, Steven L Young, Robert N Taylor, Milan K Bagchi, Indrani C Bagchi

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. ALKBH5 Positively Regulates BMP2 to Influence Endometrial Decidualization in Recurrent Spontaneous Abortion.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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  4. Review
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  7. Effects of Acrylamide on Mouse Implantation and Decidualization.International journal of molecular sciences · 2025
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  10. Review
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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

9 authors at 3 institutions in 1 country.

Shanmugasundaram NallasamyDepartment of Comparative Biosciences, University of Illinois at Urbana-Champaign, Urbana, Illinois.
Hatice S Kaya OkurDepartment of Molecular and Integrative Physiology, University of Illinois at Urbana-Champaign, Urbana, Illinois.
Arpita BhurkeDepartment of Comparative Biosciences, University of Illinois at Urbana-Champaign, Urbana, Illinois.
Juanmahel DavilaDepartment of Comparative Biosciences, University of Illinois at Urbana-Champaign, Urbana, Illinois.
Quanxi LiDepartment of Comparative Biosciences, University of Illinois at Urbana-Champaign, Urbana, Illinois.
Steven L YoungDepartment of Obstetrics and Gynecology, University of North Carolina, Chapel Hill, North Carolina.
Robert N TaylorDepartment of Obstetrics and Gynecology, University of Utah School of Medicine, Salt Lake City, Utah.
Milan K BagchiDepartment of Molecular and Integrative Physiology, University of Illinois at Urbana-Champaign, Urbana, Illinois.
Indrani C BagchiDepartment of Comparative Biosciences, University of Illinois at Urbana-Champaign, Urbana, Illinois.
University of Illinois Urbana-Champaign · USUniversity of North Carolina at Chapel Hill · USUniversity of Utah · US

Funding

Role of C/EBPb in Uterine Decidualization and ImplantationU54HD055787 · NICHD · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI BAGCHI, MILAN K · 2008 to 2012
$6.8M
NICHD NIH HHS U54 HD055787
6 · The paper itself

Abstract

Endometrial stromal cells differentiate to form decidual cells in a process known as decidualization, which is critical for embryo implantation and successful establishment of pregnancy. We previously reported that bone morphogenetic protein 2 (BMP2) mediates uterine stromal cell differentiation in mice and in humans. To identify the downstream target(s) of BMP2 signaling during decidualization, we performed gene-expression profiling of mouse uterine stromal cells, treated or not treated with recombinant BMP2. Our studies revealed that expression of Msx2, a member of the mammalian Msx homeobox gene family, was markedly upregulated in response to exogenous BMP2. Interestingly, conditional ablation of Msx2 in the uterus failed to prevent a decidual phenotype, presumably because of functional compensation of Msx2 by Msx1, a closely related member of the Msx family. Indeed, in Msx2-null uteri, the level of Msx1 expression in the stromal cells was markedly elevated. When conditional, tissue-specific ablation of both Msx1 and Msx2 was accomplished in the mouse uterus, a dramatically impaired decidual response was observed. In the absence of both Msx1 and Msx2, uterine stromal cells were able to proliferate, but they failed to undergo terminal differentiation. In parallel experiments, addition of BMP2 to human endometrial stromal cell cultures led to a robust enhancement of MSX1 and MSX2 expression and stimulated the differentiation process. Attenuation of MSX1 and MSX2 expression by small interfering RNAs greatly reduced human stromal differentiation in vitro, indicating a conservation of their roles as key mediators of BMP2-induced decidualization in mice and women.

Indexed as

AnimalsBone Morphogenetic Protein 2Cell DifferentiationEmbryo ImplantationEndometriumFemaleHomeodomain ProteinsHumansMiceMice, KnockoutMSX1 Transcription FactorSignal TransductionStromal CellsBone Morphogenetic Protein 2Homeodomain ProteinsMsx1 protein, mouseMSX1 Transcription FactorMSX2 protein

Identifiers

PMID31125045
PMCPMC6591014
OpenAlexW2945858558

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.