Evidence map›Paper›PMID 26554899›Full record

ArticleeLife2015

Generation of an expandable intermediate mesoderm restricted progenitor cell line from human pluripotent stem cells.

Nathan Kumar, Jenna Richter, Josh Cutts, Kevin T Bush, Cleber Trujillo, Sanjay K Nigam, Terry Gaasterland, David Brafman, Karl Willert

Open access · goldAbstract read
In one paragraph

Article in eLife, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  5. Mesodermal Derivatives of Pluripotent Stem Cells Route to Scarless Healing.International journal of molecular sciences · 2023
    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.

Nathan KumarDepartment of Cellular and Molecular Medicine, University of California, San Diego, San Diego, United States.
Jenna RichterDepartment of Cellular and Molecular Medicine, University of California, San Diego, San Diego, United States.
Josh CuttsSchool of Biological and Health Systems Engineering, Arizona State University, Tempe, United States.
Kevin T BushDepartment of Pediatrics, University of California, San Diego, San Diego, United States.ORCID http://orcid.org/0000-0001-5889-2847
Cleber TrujilloDepartment of Pediatrics, University of California, San Diego, San Diego, United States.
Sanjay K NigamDepartment of Cellular and Molecular Medicine, University of California, San Diego, San Diego, United States.
Terry GaasterlandScripps Institution of Oceanography, Scripps Genome Center, University of California, San Diego, San Diego, United States.
David BrafmanSchool of Biological and Health Systems Engineering, Arizona State University, Tempe, United States.
Karl WillertDepartment of Cellular and Molecular Medicine, University of California, San Diego, San Diego, United States.
University of California San Diego · USArizona State University · USScripps Institution of Oceanography · US

Funding

Epigenetic strategies for the in vitro generation of replacement beta cellsU01DK089567 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SANDER, MAIKE · 2010 to 2013
$4.7M
NIDDK NIH HHS U01 DK089567NIDDK NIH HHS U01-DK089567
6 · The paper itself

Abstract

The field of tissue engineering entered a new era with the development of human pluripotent stem cells (hPSCs), which are capable of unlimited expansion whilst retaining the potential to differentiate into all mature cell populations. However, these cells harbor significant risks, including tumor formation upon transplantation. One way to mitigate this risk is to develop expandable progenitor cell populations with restricted differentiation potential. Here, we used a cellular microarray technology to identify a defined and optimized culture condition that supports the derivation and propagation of a cell population with mesodermal properties. This cell population, referred to as intermediate mesodermal progenitor (IMP) cells, is capable of unlimited expansion, lacks tumor formation potential, and, upon appropriate stimulation, readily acquires properties of a sub-population of kidney cells. Interestingly, IMP cells fail to differentiate into other mesodermally-derived tissues, including blood and heart, suggesting that these cells are restricted to an intermediate mesodermal fate.

Indexed as

Cell DifferentiationMesodermCell Culture TechniquesHumansPluripotent Stem CellsStem CellsTissue Engineeringarrayed cellular microenvironmentdevelopmental biologydifferentiationhumanintermediate mesodermpluripotent stem cellstem cells

Identifiers

PMID26554899
PMCPMC4631902
OpenAlexW2153428674

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.