Evidence map›Paper›PMID 26140606›Full record

ArticleCell stem cell2015

Quantification of Retinogenesis in 3D Cultures Reveals Epigenetic Memory and Higher Efficiency in iPSCs Derived from Rod Photoreceptors.

Daniel Hiler, Xiang Chen, Jennifer Hazen, Sergey Kupriyanov, Patrick A Carroll, Chunxu Qu, Beisi Xu, Dianna Johnson, Lyra Griffiths, Sharon Frase and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell stem cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

64 citing papers in PubMed, 99 citations in OpenAlex.

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  7. Article
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  12. Retinal Organoids and Retinal Prostheses: An Overview.International journal of molecular sciences · 2022
    Review
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  14. Article
  15. Article
  16. Retinal Organoid Technology: Where Are We Now?International journal of molecular sciences · 2021
    Review
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  18. Article
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  20. Review

4 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

19 authors at 4 institutions in 1 country.

Daniel HilerDepartment of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Xiang ChenDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Jennifer HazenDepartment of Cell Biology, The Scripps Research Institute, La Jolla, CA 92037, USA.
Sergey KupriyanovMouse Genetics Core Facility, The Scripps Research Institute, La Jolla, CA 92037, USA.
Patrick A CarrollDivision of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA 98108, USA.
Chunxu QuDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Beisi XuDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Dianna JohnsonDepartment of Ophthalmology, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Lyra GriffithsDepartment of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Sharon FraseCell and Tissue Imaging Shared Resource, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Alberto R RodriguezMouse Genetics Core Facility, The Scripps Research Institute, La Jolla, CA 92037, USA.
Greg MartinMouse Genetics Core Facility, The Scripps Research Institute, La Jolla, CA 92037, USA.
Jiakun ZhangDepartment of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Jongrye JeonDepartment of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Yiping FanDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
David FinkelsteinDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Robert N EisenmanDivision of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA 98108, USA.
Kristin BaldwinDepartment of Cell Biology, The Scripps Research Institute, La Jolla, CA 92037, USA.
Michael A DyerDepartment of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA; Department of Ophthalmology, University of Tennessee Health Science Center, Memphis, TN 38163, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA. Electronic address: michael.dyer@stjude.org.
St. Jude Children's Research Hospital · USScripps Research Institute · USFred Hutch Cancer Center · USUniversity of Tennessee Health Science Center · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI SUZANNE J. BAKER · 1985 to 2026
$166.9M
Regulation of cell growth and proliferation by MycR01CA020525 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI EISENMAN, ROBERT NEIL · 1985 to 2018
$10.7M
Chromosome Metabolism and Cancer Training GrantT32CA009657 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI EISENMAN, ROBERT NEIL · 1991 to 2020
$7.6M
Proliferation Control in the Retina: The Rb FamilyR01EY014867 · NEI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI DYER, MICHAEL A · 2003 to 2012
$4.5M
Genome-wide investigation of somatic mutation in the developing and aging brainR01MH102698 · NIMH · SCRIPPS RESEARCH INSTITUTE, THE · PI BALDWIN, KRISTIN KAY, HALL, IRA M · 2014 to 2018
$3.4M
Proliferation and Differentiation of Retinal Stem CellsR01EY018599 · NEI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI DYER, MICHAEL A · 2008 to 2011
$2.5M
The architecture and development of a sensory processing circuit for smellR01DC012592 · NIDCD · SCRIPPS RESEARCH INSTITUTE, THE · PI BALDWIN, KRISTIN KAY · 2012 to 2016
$2.3M
Epigenetic Reprogramming of Retinal NeuronsR01EY023619 · NEI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI DYER, MICHAEL A · 2013 to 2017
$2.2M
Molecular Targeted Therapy for RetinoblastomaR01CA168875 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI DYER, MICHAEL A · 2012 to 2016
$1.8M
Howard Hughes Medical InstituteNCI NIH HHS CA168875NCI NIH HHS CA21765NCI NIH HHS P30 CA021765NCI NIH HHS R01 CA020525NCI NIH HHS R01 CA168875NCI NIH HHS R01CA20525NCI NIH HHS T32 CA009657NEI NIH HHS EY014867NEI NIH HHS EY018599NEI NIH HHS R01 EY014867NEI NIH HHS R01 EY018599NEI NIH HHS R01 EY023619NIDCD NIH HHS R01 DC012592NIMH NIH HHS R01 MH102698
6 · The paper itself

Abstract

Cell-based therapies to treat retinal degeneration are now being tested in clinical trials. However, it is not known whether the source of stem cells is important for the production of differentiated cells suitable for transplantation. To test this, we generated induced pluripotent stem cells (iPSCs) from murine rod photoreceptors (r-iPSCs) and scored their ability to make retinae by using a standardized quantitative protocol called STEM-RET. We discovered that r-iPSCs more efficiently produced differentiated retinae than did embryonic stem cells (ESCs) or fibroblast-derived iPSCs (f-iPSCs). Retinae derived from f-iPSCs had fewer amacrine cells and other inner nuclear layer cells. Integrated epigenetic analysis showed that DNA methylation contributes to the defects in f-iPSC retinogenesis and that rod-specific CTCF insulator protein-binding sites may promote r-iPSC retinogenesis. Together, our data suggest that the source of stem cells is important for producing retinal neurons in three-dimensional (3D) organ cultures.

Indexed as

Epigenesis, GeneticAnimalsCell Culture TechniquesCell DifferentiationCell LineCellular ReprogrammingDNA MethylationEmbryonic Stem CellsHumansInduced Pluripotent Stem CellsMiceMice, TransgenicRetinaRetinal DegenerationRetinal Rod Photoreceptor Cells

Identifiers

PMID26140606
PMCPMC4547539
OpenAlexW1522174931

What OpenQuestion holds

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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.