Evidence map›Paper›PMID 22396540›Full record

ArticleThe Journal of biological chemistry2012

Meiotic competent human germ cell-like cells derived from human embryonic stem cells induced by BMP4/WNT3A signaling and OCT4/EpCAM (epithelial cell adhesion molecule) selection.

Ching-Yu Chuang, Kuo-I Lin, Michael Hsiao, Lee Stone, Hsin-Fu Chen, Yen-Hua Huang, Shau-Ping Lin, Hong-Nerng Ho, Hung-Chih Kuo

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Review
  3. The Role of Bone Morphogenetic Protein 4 in Ovarian Function and Diseases.Reproductive sciences (Thousand Oaks, Calif.) · 2021
    Review
  4. Review
  5. Roles of MicroRNAs in Establishing and Modulating Stem Cell Potential.International journal of molecular sciences · 2019
    Review
  6. A novel role forDevelopment (Cambridge, England) · 2018
    Article
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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 6 institutions in 3 countries.

Ching-Yu ChuangGenomics Research Center, Academia Sinica, Taipei 115, Taiwan.
Kuo-I Lin
Michael Hsiao
Lee Stone
Hsin-Fu Chen
Yen-Hua Huang
Shau-Ping Lin
Hong-Nerng Ho
Hung-Chih Kuo
Genomics (United Kingdom) · GBAgricultural Biotechnology Research Center, Academia Sinica · TWInstitute of Cellular and Organismic Biology, Academia Sinica · TWNational Taiwan University · TWNational Taiwan University Hospital · TWTaipei Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The establishment of an effective germ cell selection/enrichment platform from in vitro differentiating human embryonic stem cells (hESCs) is crucial for studying the molecular and signaling processes governing human germ cell specification and development. In this study, we developed a germ cell-enriching system that enables us to identify signaling factors involved in germ cell-fate induction from differentiating hESCs in vitro. First, we demonstrated that selection through an OCT4-EGFP reporter system can successfully increase the percentage of meiotic-competent, germ cell-like cells from spontaneously differentiating hESCs. Furthermore, we showed that the pluripotency associated surface marker, epithelial cell adhesion molecule (EpCAM), is also expressed in human fetal gonads and can be used as an effective selection marker for germ cell enrichment from differentiating hESCs. Combining OCT4 and EpCAM selection can further enrich the meiotic-competent germ cell-like cell population. Also, with the percentage of OCT4(+)/EpCAM(+) cells as readout, we demonstrated the synergistic effect of BMP4/pSMAD1/5/8 and WNT3A/β-CATENIN in promoting hESCs toward the germline fate. Combining BMP4/WNT3A induction and OCT4/EpCAM selection can significantly increase the putative germ cell population with meiotic competency. Co-transplantation of these cells with dissociated mouse neonatal ovary cells into SCID mice resulted in a homogenous germ cell cluster formation in vivo. The stepwise platform established in this study provides a useful tool to elucidate the molecular mechanisms of human germ cell development, which has implications not only for human fertility research but regenerative medicine in general.

Indexed as

AnimalsAntigens, Neoplasmbeta CateninBone Morphogenetic Protein 4Cell Adhesion MoleculesCell DifferentiationEmbryonic Stem CellsEpithelial Cell Adhesion MoleculeFemaleGerm CellsHumansMeiosisMiceMice, SCIDOctamer Transcription Factor-3Pluripotent Stem CellsAntigens, Neoplasmbeta CateninBMP4 protein, humanBone Morphogenetic Protein 4Cell Adhesion MoleculesEPCAM protein, humanEpithelial Cell Adhesion MoleculeOctamer Transcription Factor-3POU5F1 protein, humanWnt3A ProteinWNT3A protein, human

Identifiers

PMID22396540
PMCPMC3340282
OpenAlexW2068655353

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.