Evidence map›Paper›PMID 25002137›Full record

ArticleBMC research notes2014

Aneuploidy is permissive for hepatocyte-like cell differentiation from human induced pluripotent stem cells.

Fallon K Noto, Megan R Determan, Jun Cai, Max A Cayo, Sunil K Mallanna, Stephen A Duncan

Open access · goldAbstract read
In one paragraph

Article in BMC research notes, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Fallon K Noto
Megan R Determan
Jun Cai
Max A Cayo
Sunil K Mallanna
Stephen A DuncanDepartment of Cell Biology, Neurobiology and Anatomy, The Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI 53226, USA. duncans@mcw.edu.
Medical College of Wisconsin · US

Funding

iPS-derived hepatocytes for interrogation of lipid phenotypesU01HG006398 · NHGRI · UNIVERSITY OF PENNSYLVANIA · PI RADER, DANIEL JAMES · 2011 to 2015
$8.6M
TRANSCRIPTIONAL REGULAT OF MAMMALIAN HEPATIC DEVELOPMENTR01DK055743 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI DUNCAN, STEPHEN A · 2000 to 2014
$4.6M
Molecular Basis of Human Hepatic Progenitor Cell FormationR01DK102716 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI DUNCAN, STEPHEN A · 2014 to 2022
$3.8M
iPS-derived hepatocytes as a model of familial hypercholesterolemiaF30DK091994 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI CAYO, MAX A · 2011 to 2016
$258k
A Study of the Cellular Mechanisms Causing Progression to Diabetes in HNF1A-MODYF30DK098926 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI DETERMAN, MEGAN R · 2013 to 2016
$173k
Role of GATA4 and GATA6 in Controlling Heart DevelopmentR01HL094857 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI DUNCAN, STEPHEN A · 2009 to 2009
$110k
Treating liver dysfunction with induced pluripotent stem cell-derived hepatocytesF31AA019874 · NIAAA · MEDICAL COLLEGE OF WISCONSIN · PI NOTO, FALLON K · 2010 to 2012
$107k
NHGRI NIH HHS HG006398NHGRI NIH HHS U01 HG006398NHLBI NIH HHS HL094857NIAAA NIH HHS AA019874NIDDK NIH HHS DK091994NIDDK NIH HHS DK098926NIDDK NIH HHS DK55743NIDDK NIH HHS R01 DK102716
6 · The paper itself

Abstract

backgroundThe characterization of induced pluripotent stem cells (iPSCs) and embryonic stem cells (ESCs) routinely includes analyses of chromosomal integrity. The belief is that pluripotent stem cells best suited to the generation of differentiated derivatives should display a euploid karyotype; although, this does not appear to have been formally tested. While aneuploidy is commonly associated with cell transformation, several types of somatic cells, including hepatocytes, are frequently aneuploid and variation in chromosomal content does not contribute to a transformed phenotype. This insight has led to the proposal that dynamic changes in the chromosomal environment may be important to establish genetic diversity within the hepatocyte population and such diversity may facilitate an adaptive response by the liver to various insults. Such a positive contribution of aneuploidy to liver function raises the possibility that, in contrast to existing dogma, aneuploid iPSCs may be capable of generating hepatocyte-like cells that display hepatic activities.

resultsWe examined whether a human iPSC line that had multiple chromosomal aberrations was competent to differentiate into hepatocytes and found that loss of normal chromosomal content had little impact on the production of hepatocyte-like cells from iPSCs.

conclusionsiPSCs that harbor an abnormal chromosomal content retain the capacity to generate hepatocyte-like cells with high efficiency.

Indexed as

AneuploidyCell DifferentiationCells, CulturedGene ExpressionHepatocytesHumansInduced Pluripotent Stem CellsKaryotypeLiverPluripotent Stem CellsReverse Transcriptase Polymerase Chain Reaction

Identifiers

PMID25002137
PMCPMC4105394
OpenAlexW1998945234

What OpenQuestion holds

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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.