Evidence map›Paper›PMID 22751106›Full record

ArticleThe Journal of clinical investigation2012

Identification of embryonic stem cell-derived midbrain dopaminergic neurons for engraftment.

Yosif M Ganat, Elizabeth L Calder, Sonja Kriks, Jenny Nelander, Edmund Y Tu, Fan Jia, Daniela Battista, Neil Harrison, Malin Parmar, Mark J Tomishima and 2 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed, 1 pooled it
7.8field-weighted citation impact, top 2% 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

88 citing papers in PubMed, 1 synthesis or guideline pooled it, 141 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Stem Cell-Based Approaches in Parkinson's Disease Research.International journal of stem cells · 2025
    Review
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28 more citing papers are in PubMed but not listed here.

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

12 authors at 3 institutions in 2 countries.

Yosif M GanatCenter for Stem Cell Biology, Sloan-Kettering Institute for Cancer Research, New York, NY, USA.
Elizabeth L Calder
Sonja Kriks
Jenny Nelander
Edmund Y Tu
Fan Jia
Daniela Battista
Neil Harrison
Malin Parmar
Mark J Tomishima
Urs Rutishauser
Lorenz Studer
Kettering University · USColumbia University · USRegenerative Medicine Institute · MX

Funding

Human embryonic stem cell derived midbrain dopamine neuronsR01NS052671 · NINDS · SLOAN-KETTERING INST CAN RESEARCH · PI STUDER, LORENZ P. · 2007 to 2010
$1.6M
NINDS NIH HHS NS052671NINDS NIH HHS R01 NS052671
6 · The paper itself

Abstract

Embryonic stem cells (ESCs) represent a promising source of midbrain dopaminergic (DA) neurons for applications in Parkinson disease. However, ESC-based transplantation paradigms carry a risk of introducing inappropriate or tumorigenic cells. Cell purification before transplantation may alleviate these concerns and enable identification of the specific DA neuron stage most suitable for cell therapy. Here, we used 3 transgenic mouse ESC reporter lines to mark DA neurons at 3 stages of differentiation (early, middle, and late) following induction of differentiation using Hes5::GFP, Nurr1::GFP, and Pitx3::YFP transgenes, respectively. Transplantation of FACS-purified cells from each line resulted in DA neuron engraftment, with the mid-stage and late-stage neuron grafts being composed almost exclusively of midbrain DA neurons. Mid-stage neuron cell grafts had the greatest amount of DA neuron survival and robustly induced recovery of motor deficits in hemiparkinsonian mice. Our data suggest that the Nurr1+ stage (middle stage) of neuronal differentiation is particularly suitable for grafting ESC-derived DA neurons. Moreover, global transcriptome analysis of progeny from each of the ESC reporter lines revealed expression of known midbrain DA neuron genes and also uncovered previously uncharacterized midbrain genes. These data demonstrate remarkable fate specificity of ESC-derived DA neurons and outline a sequential stage-specific ESC reporter line paradigm for in vivo gene discovery.

Indexed as

AnimalsCell DifferentiationCell LineCell SeparationCell SurvivalDopaminergic NeuronsEmbryonic Stem CellsGenes, ReporterGraft SurvivalLuminescent ProteinsMesencephalonMiceMice, TransgenicNeural Stem CellsRecombinant ProteinsTranscriptomeLuminescent ProteinsRecombinant Proteins

Identifiers

PMID22751106
PMCPMC3408729
OpenAlexW1998801756

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.