Evidence map›Paper›PMID 28009074›Full record

ArticleStem cells (Dayton, Ohio)2017

New Monoclonal Antibodies to Defined Cell Surface Proteins on Human Pluripotent Stem Cells.

Carmel M O'Brien, Hun S Chy, Qi Zhou, Shiri Blumenfeld, Jack W Lambshead, Xiaodong Liu, Joshua Kie, Bianca D Capaldo, Tung-Liang Chung, Timothy E Adams and 17 more

Open access · hybridAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. H1N1 influenza virus epitopes classified by monoclonal antibodies.Experimental and therapeutic medicine · 2018
    Article
  12. 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

27 authors at 11 institutions in 4 countries.

Carmel M O'BrienClayton and Parkville, CSIRO Manufacturing, Victoria, Australia.
Hun S ChyClayton and Parkville, CSIRO Manufacturing, Victoria, Australia.
Qi ZhouClayton and Parkville, CSIRO Manufacturing, Victoria, Australia.
Shiri BlumenfeldClayton and Parkville, CSIRO Manufacturing, Victoria, Australia.
Jack W LambsheadClayton and Parkville, CSIRO Manufacturing, Victoria, Australia.
Xiaodong LiuAustralian Regenerative Medicine Institute, Monash University, Clayton, Victoria, Australia.
Joshua KieClayton and Parkville, CSIRO Manufacturing, Victoria, Australia.
Bianca D CapaldoThe Walter and Eliza Hall Institute (WEHI), Parkville, Victoria, Australia.
Tung-Liang ChungClayton and Parkville, CSIRO Manufacturing, Victoria, Australia.
Timothy E AdamsClayton and Parkville, CSIRO Manufacturing, Victoria, Australia.
Tram PhanClayton and Parkville, CSIRO Manufacturing, Victoria, Australia.
John D BentleyClayton and Parkville, CSIRO Manufacturing, Victoria, Australia.
William J McKinstryClayton and Parkville, CSIRO Manufacturing, Victoria, Australia.
Karen OlivaDepartment of Surgery, Cabrini Monash University, Malvern, Victoria, Australia.
Paul J McMurrickDepartment of Surgery, Cabrini Monash University, Malvern, Victoria, Australia.
Yu-Chieh WangDepartment of Chemical Physiology.
Fernando J RosselloAustralian Regenerative Medicine Institute, Monash University, Clayton, Victoria, Australia.
Geoffrey J LindemanThe Walter and Eliza Hall Institute (WEHI), Parkville, Victoria, Australia.
Di ChenDepartment of Molecular, Cell and Developmental Biology, University of California, Los Angeles, California, USA.
Thierry JardeDepartment of Anatomy and Developmental Biology, Monash University, Clayton, Victoria, Australia.
Amander T ClarkDepartment of Molecular, Cell and Developmental Biology, University of California, Los Angeles, California, USA.
Helen E AbudDepartment of Anatomy and Developmental Biology, Monash University, Clayton, Victoria, Australia.
Jane E VisvaderThe Walter and Eliza Hall Institute (WEHI), Parkville, Victoria, Australia.
Christian M NefzgerAustralian Regenerative Medicine Institute, Monash University, Clayton, Victoria, Australia.
Jose M PoloAustralian Regenerative Medicine Institute, Monash University, Clayton, Victoria, Australia.
Jeanne F LoringDepartment of Chemical Physiology.
Andrew L LaslettClayton and Parkville, CSIRO Manufacturing, Victoria, Australia.
CSIRO Manufacturing · AUMonash University · AUAustralian Regenerative Medicine Institute · AUCabrini Hospital · AUDiscovery Institute · USUniversity of California, Los Angeles · USCzech Academy of Sciences, Institute of Physiology · CZDepartment of Medical Sciences · RUScripps Research Institute · USUniversity of Melbourne · AUWalter and Eliza Hall Institute of Medical Research · AU

Funding

Differentiating embryonic stem cells into developing germ lineR01HD079546 · NICHD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CLARK, AMANDER · 2015 to 2024
$3.7M
NICHD NIH HHS R01 HD079546
6 · The paper itself

Abstract

The study and application of human pluripotent stem cells (hPSCs) will be enhanced by the availability of well-characterized monoclonal antibodies (mAbs) detecting cell-surface epitopes. Here, we report generation of seven new mAbs that detect cell surface proteins present on live and fixed human ES cells (hESCs) and human iPS cells (hiPSCs), confirming our previous prediction that these proteins were present on the cell surface of hPSCs. The mAbs all show a high correlation with POU5F1 (OCT4) expression and other hPSC surface markers (TRA-160 and SSEA-4) in hPSC cultures and detect rare OCT4 positive cells in differentiated cell cultures. These mAbs are immunoreactive to cell surface protein epitopes on both primed and naive state hPSCs, providing useful research tools to investigate the cellular mechanisms underlying human pluripotency and states of cellular reprogramming. In addition, we report that subsets of the seven new mAbs are also immunoreactive to human bone marrow-derived mesenchymal stem cells (MSCs), normal human breast subsets and both normal and tumorigenic colorectal cell populations. The mAbs reported here should accelerate the investigation of the nature of pluripotency, and enable development of robust cell separation and tracing technologies to enrich or deplete for hPSCs and other human stem and somatic cell types. Stem Cells 2017;35:626-640.

Indexed as

AnimalsAntibodies, MonoclonalAntigens, SurfaceCell Culture TechniquesCell DifferentiationCell Self RenewalDown-RegulationEmbryoid BodiesFlow CytometryHematopoietic Stem CellsHumansMembrane ProteinsMiceOctamer Transcription Factor-3Pluripotent Stem CellsAntibodies, MonoclonalAntigens, SurfaceMembrane ProteinsOctamer Transcription Factor-3BreastCancerCell surface markersColorectalHuman embryonic stem cellsHuman iPS cellsMonoclonal antibodiesNaivePluripotency

Identifiers

PMID28009074
PMCPMC5412944
OpenAlexW2562295517

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.