Evidence map›Paper›PMID 19500897›Full record

ArticleDifferentiation; research in biological diversity2009

Renal ontogeny in the rhesus monkey (Macaca mulatta) and directed differentiation of human embryonic stem cells towards kidney precursors.

Cynthia A Batchelder, C Chang I Lee, Douglas G Matsell, Mervin C Yoder, Alice F Tarantal

Abstract read
In one paragraph

Article in Differentiation; research in biological diversity, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

43 citing papers in PubMed, 78 citations in OpenAlex.

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  15. Article
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  17. Review
  18. Bioengineering kidneys for transplantation.Seminars in nephrology · 2014
    Review
  19. Article
  20. Bone morphogenetic protein signaling in nephron progenitor cells.Pediatric nephrology (Berlin, Germany) · 2014
    Review
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

5 authors at 2 institutions in 2 countries.

Cynthia A BatchelderCenter of Excellence in Translational Human Stem Cell Research, University of California, Davis, CA, USA.
C Chang I Lee
Douglas G Matsell
Mervin C Yoder
Alice F Tarantal
University of California, Davis · USChild and Family Research Institute · CA

Funding

ZONA PELLUCIDA PEPTIDES AS IMMUNOCONTRACEPTIVE ANTIGENSP51RR000169 · NCRR · UNIVERSITY OF CALIFORNIA DAVIS · PI HYDE, DALLAS MELVIN · 1985 to 2011
$126.2M
Transplant and Imaging of Human Stem and Progenitor Cells in Nonhuman PrimatesP50HL085036 · NHLBI · UNIVERSITY OF CALIFORNIA DAVIS · PI YODER, MERVIN C. · 2005 to 2008
$5.8M
Supplement to Center for Fetal Monkey Gene TransferU01HL069748 · NHLBI · UNIVERSITY OF CALIFORNIA DAVIS · PI TARANTAL, ALICE F · 2001 to 2005
$3.5M
NCRR NIH HHS P51 RR000169NCRR NIH HHS RR00169NHLBI NIH HHS HL069748NHLBI NIH HHS P50 HL085036NHLBI NIH HHS U01 HL069748
6 · The paper itself

Abstract

The development of the metanephric kidney was studied immunohistochemically across gestation in monkeys to identify markers of cell specification, and to aid in developing experimental paradigms for renal precursor differentiation from human embryonic stem cells (hESC). PAX2, an important kidney developmental marker, was expressed at the tips of the ureteric bud, in the surrounding condensing mesenchyme, and in the renal vesicle. Vimentin, a mesenchymal and renal marker, was strongly expressed in the metanephric blastema then found to be limited to the glomerulus and interstitial cells of the medulla and cortex. A model of gene expression based on human and nonhuman primate renal ontogeny was developed and incorporated into studies of hESC differentiation. Spontaneous hESC differentiation revealed markers of metanephric mesenchyme (OSR1, PAX2, SIX2, WT1) that increased over time, followed by upregulation of kidney precursor markers (EYA1, LIM1, CD24). Directed hESC differentiation was also evaluated with the addition of retinoic acid, Activin-A, and BMP-4 or BMP-7, and using different culture substrate conditions. Of the culture substrates studied, gelatin most closely recapitulated the anticipated directed developmental pattern of renal gene expression. No differences were found when BMP-4 and BMP-7 were compared with baseline conditions. PAX2 and Vimentin immunoreactivity in differentiating hESC was also similar to the renal precursor patterns reported for human fetal kidneys and findings described in rhesus monkeys. The results of these studies are as follows: (1) provide additional data to support that rhesus monkey kidney development parallels that of humans, and (2) provide a useful model for hESC directed differentiation towards renal precursors.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsCell DifferentiationCells, CulturedEmbryonic Stem CellsFluorescent Antibody Technique, DirectFluorescent DyesHumansImmunohistochemistryIndolesKidneyMacaca mulattaMesodermPAX2 Transcription FactorVimentinDAPIFluorescent DyesIndolesPAX2 Transcription FactorVimentin

Identifiers

PMID19500897
PMCPMC2744219
OpenAlexW2050741251

What OpenQuestion holds

Textmetadata
LicenceTDM
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.