Evidence map›Paper›PMID 27404995›Full record

ArticleJournal of visualized experiments : JoVE2016

Promoting 3-D Aggregation of FACS Purified Thymic Epithelial Cells with EAK 16-II/EAKIIH6 Self-assembling Hydrogel.

Asako Tajima, Wen Liu, Isha Pradhan, Suzanne Bertera, Robert A Lakomy, William A Rudert, Massimo Trucco, Wilson S Meng, Yong Fan

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Recent Advancements in Regenerative Approaches for Thymus Rejuvenation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Review
  4. Article
  5. Review
  6. Article
  7. 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

9 authors at 4 institutions in 3 countries.

Asako TajimaInstitute of Cellular Therapeutics, Allegheny Health Network.
Wen LiuDivision of Pharmaceutical Sciences, Mylan School of Pharmacy, Duquesne University.
Isha PradhanInstitute of Cellular Therapeutics, Allegheny Health Network.
Suzanne BerteraInstitute of Cellular Therapeutics, Allegheny Health Network.
Robert A LakomyInstitute of Cellular Therapeutics, Allegheny Health Network.
William A RudertInstitute of Cellular Therapeutics, Allegheny Health Network.
Massimo TruccoInstitute of Cellular Therapeutics, Allegheny Health Network; Department of Biological Sciences, Carnegie Mellon University.
Wilson S MengDivision of Pharmaceutical Sciences, Mylan School of Pharmacy, Duquesne University.
Yong FanInstitute of Cellular Therapeutics, Allegheny Health Network; Department of Biological Sciences, Carnegie Mellon University; yong.fan74@gmail.com.
Cellular Therapeutics (United Kingdom) · GBAllegheny Health Network · USCarnegie Mellon University · USDuquesne University · US

Funding

Induction of allogeneic tolerance with bioengineered thymus organoidsR01AI123392 · NIAID · ALLEGHENY-SINGER RESEARCH INSTITUTE · PI FAN, YONG · 2016 to 2019
$1.5M
A Biomaterial Approach to Attenuate Rejection of Skin AllograftsR21AI113000 · NIAID · DUQUESNE UNIVERSITY · PI MENG, WILSON S · 2014 to 2015
$320k
NIAID NIH HHS R01 AI123392NIAID NIH HHS R21 AI113000
6 · The paper itself

Abstract

Thymus involution, associated with aging or pathological insults, results in diminished output of mature T-cells. Restoring the function of a failing thymus is crucial to maintain effective T cell-mediated acquired immune response against invading pathogens. However, thymus regeneration and revitalization proved to be challenging, largely due to the difficulties of reproducing the unique 3D microenvironment of the thymic stroma that is critical for the survival and function of thymic epithelial cells (TECs). We developed a novel hydrogel system to promote the formation of TEC aggregates, based on the self-assembling property of the amphiphilic EAK16-II oligopeptides and its histidinylated analogue EAKIIH6. TECs were enriched from isolated thymic cells with density-gradient, sorted with fluorescence-activated cell sorting (FACS), and labeled with anti-epithelial cell adhesion molecule (EpCAM) antibodies that were anchored, together with anti-His IgGs, on the protein A/G adaptor complexes. Formation of cell aggregates was promoted by incubating TECs with EAKIIH6 and EAK16-II oligopeptides, and then by increasing the ionic concentration of the medium to initiate gelation. TEC aggregates embedded in EAK hydrogel can effectively promote the development of functional T cells in vivo when transplanted into the athymic nude mice.

Indexed as

Epithelial CellsAnimalsHydrogel, Polyethylene Glycol DimethacrylateMiceMice, NudeOligopeptidesThymus GlandT-LymphocytesHydrogel, Polyethylene Glycol DimethacrylateOligopeptides

Identifiers

PMID27404995
PMCPMC4993281
OpenAlexW2468279678

What OpenQuestion holds

Textmetadata
LicenceTDM
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.