Evidence map›Paper›PMID 30222162›Full record

ArticleJournal of visualized experiments : JoVE2018

Isolation of Human Endometrial Stromal Cells for In Vitro Decidualization.

Stephanie A Michalski, Sangappa B Chadchan, Emily S Jungheim, Ramakrishna Kommagani

Open access · bronzeAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Signaling via retinoic acid receptors mediates decidual angiogenesis in mice and human stromal cell decidualization.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Strategies for modelling endometrial diseases.Nature reviews. Endocrinology · 2022
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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

4 authors at 1 institution in 1 country.

Stephanie A MichalskiDepartment of Obstetrics and Gynecology, Center for Reproductive Health Sciences, Washington University School of Medicine.
Sangappa B ChadchanDepartment of Obstetrics and Gynecology, Center for Reproductive Health Sciences, Washington University School of Medicine.
Emily S JungheimDepartment of Obstetrics and Gynecology, Center for Reproductive Health Sciences, Washington University School of Medicine.
Ramakrishna KommaganiDepartment of Obstetrics and Gynecology, Center for Reproductive Health Sciences, Washington University School of Medicine; kommagani@wustl.edu.
University of Washington · US

Funding

GREB1 Action in Endometrial Function and DysfunctionR00HD080742 · NICHD · WASHINGTON UNIVERSITY · PI KOMMAGANI, RAMAKRISHNA · 2017 to 2019
$702k
GREB1 Action in Endometrial Function and DysfunctionK99HD080742 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI KOMMAGANI, RAMAKRISHNA · 2015 to 2016
$221k
NICHD NIH HHS K99 HD080742NICHD NIH HHS R00 HD080742
6 · The paper itself

Abstract

The differentiation of human endometrial stromal cells (HESC) from fibroblast-like appearance into secretory decidua is a transformation required for embryo implantation into the uterine lining of the maternal womb. Improper decidualization has been established as a root cause for implantation failure and subsequent early embryo miscarriage. Therefore, understanding the molecular mechanisms underlying decidualization is advantageous to improving the rate of successful births. In vivo based studies of artificial decidualization are often limiting due to ethical dilemmas associated with human research, as well as translational complications within animal models. As a result, in vitro assays through primary cell culture are often utilized to explore the modulation of decidualization via hormones. This study provides a detailed protocol for the isolation of HESC and subsequent artificial decidualization via the supplementation of hormones to the culturing medium. Further, this study provides a well-designed method to knockdown any gene of interest by utilizing lipid-based siRNA transfections. This protocol permits the optimization of culture purity as well as product yield, thereby maximizing the ability to utilize this model as a reliable method to understand the molecular mechanisms underlying decidualization, and the subsequent quantification of secreted agents by decidualized endometrial stromal cells.

Indexed as

Cell DifferentiationCells, CulturedDeciduaEndometriumFemaleHumansStromal CellsTransfection

Identifiers

PMID30222162
PMCPMC6235076
OpenAlexW2889314620

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.