Evidence map›Paper›PMID 24182315›Full record

ArticleCellular reprogramming2013

Derivation of induced pluripotent stem cells from the baboon: a nonhuman primate model for preclinical testing of stem cell therapies.

Christopher S Navara, Jacey Hornecker, Douglas Grow, Shital Chaudhari, Peter J Hornsby, Justin K Ichida, Kevin Eggan, John R McCarrey

Abstract read
In one paragraph

Article in Cellular reprogramming, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.7field-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

15 citing papers in PubMed, 27 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

8 authors at 3 institutions in 2 countries.

Christopher S Navara1 Department of Biology, University of Texas at San Antonio , San Antonio, TX 78249.
Jacey Hornecker
Douglas Grow
Shital Chaudhari
Peter J Hornsby
Justin K Ichida
Kevin Eggan
John R McCarrey
The University of Texas at San Antonio · USHarvard Stem Cell Institute · USLaboratoire d’immunologie intégrative du cancer · FR

Funding

The Southwest National Primate Research Center Supplement- Infrastructure improvements of ABSL2 holding areasP51OD011133 · OD · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI Larry S. Schlesinger · 2012 to 2026
$129.7M
Regulatory Roles and Dynamics of Nuclear long-noncoding RNAs in PluripotencyP01GM099117 · NIGMS · HARVARD UNIVERSITY · PI MEISSNER, ALEXANDER · 2011 to 2021
$21.2M
Developmental Reprogramming after Nuclear TransferR01HD046732 · NICHD · HARVARD UNIVERSITY · PI EGGAN, KEVIN C · 2005 to 2013
$3.1M
Conversion of Fibroblasts to fxnal Spinal Motor Neurons Using Defined FactorR00NS077435 · NINDS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ICHIDA, JUSTIN KAWIKA · 2013 to 2015
$737k
Derivation and Characterization of Baboon ES CellsR21RR022865 · NCRR · UNIVERSITY OF TEXAS SAN ANTONIO · PI MCCARREY, JOHN R · 2006 to 2007
$384k
NCRR NIH HHS RR022865NICHD NIH HHS HD046732NIGMS NIH HHS GM099117NIH HHS P51 OD011133NINDS NIH HHS R00 NS077435
6 · The paper itself

Abstract

Development of effective pluripotent stem cell-based therapies will require safety and efficacy testing in a clinically relevant preclinical model such as nonhuman primates (NHPs). Baboons and macaques are equally similar to humans genetically and both have been extensively used for biomedical research. Macaques are preferred for human immunodeficiency virus/acquired immunodeficiency syndrome (HIV/AIDS) research whereas baboons are preferred for transplantation studies because of the greater similarity of their anatomy and immunogenetic system to those of humans. We generated four induced pluripotent stem cell (iPSC) lines from skin cells of the olive baboon (Papio anubis). Each line shows the distinct morphology of primate pluripotent stem cells, including flat colonies with well-defined borders and a high nuclear/cytoplasm ratio. Each is positive for the pluripotency markers OCT4, SOX2, NANOG, and SSEA4. Pluripotency was confirmed in two lines by teratoma formation with representative tissues from each germ layer, whereas a third produced cells from all three germ layers following embryoid body differentiation. Three lines have a normal male karyotype and the fourth is missing the short arm of one copy of chromosome 18. This may serve as an in vitro model for the human developmental disorder 18p-, which impacts 1 in 50,000 births/year. These iPSC lines represent the first step toward establishing the baboon as a NHP model for developing stem cell-based therapies.

Indexed as

Models, AnimalStem Cell TransplantationAnimalsBase SequenceBiomarkersDNA PrimersInduced Pluripotent Stem CellsKaryotypingPapioPolymerase Chain ReactionBiomarkersDNA Primers

Identifiers

PMID24182315
PMCPMC3848439
OpenAlexW2106923599

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.