Evidence map›Paper›PMID 30723213›Full record

ArticleNature communications2019

Generation of pluripotent stem cell-derived mouse kidneys in Sall1-targeted anephric rats.

Teppei Goto, Hiromasa Hara, Makoto Sanbo, Hideki Masaki, Hideyuki Sato, Tomoyuki Yamaguchi, Shinichi Hochi, Toshihiro Kobayashi, Hiromitsu Nakauchi, Masumi Hirabayashi

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing 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

67 citing papers in PubMed, 119 citations in OpenAlex.

  1. The making of cells and organs in xenogeneic animal bioreactor.Signal transduction and targeted therapy · 2026
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  8. Xenophagocytosis blockade enhances interspecies chimerism.bioRxiv : the preprint server for biology · 2025
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  18. Parathyroid Gland Generation from Pluripotent Stem Cells.Endocrinology and metabolism (Seoul, Korea) · 2024
    Review
  19. Article
  20. Article

7 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 2 countries.

Teppei GotoCenter for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki, 444-8787, Aichi, Japan.ORCID http://orcid.org/0000-0002-0081-3357
Hiromasa HaraCenter for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki, 444-8787, Aichi, Japan.
Makoto SanboCenter for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki, 444-8787, Aichi, Japan.
Hideki MasakiDivision of Stem Cell Therapy, Institute of Medical Science, The University of Tokyo, Minato-ku, 108-8639, Tokyo, Japan.
Hideyuki SatoDivision of Stem Cell Therapy, Institute of Medical Science, The University of Tokyo, Minato-ku, 108-8639, Tokyo, Japan.
Tomoyuki YamaguchiDivision of Stem Cell Therapy, Institute of Medical Science, The University of Tokyo, Minato-ku, 108-8639, Tokyo, Japan.ORCID http://orcid.org/0000-0002-3070-2885
Shinichi HochiFaculty of Textile Science and Technology, Shinshu University, Ueda, 386-8567, Nagano, Japan.
Toshihiro KobayashiCenter for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki, 444-8787, Aichi, Japan.
Hiromitsu NakauchiDivision of Stem Cell Therapy, Institute of Medical Science, The University of Tokyo, Minato-ku, 108-8639, Tokyo, Japan.
Masumi HirabayashiCenter for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki, 444-8787, Aichi, Japan. mhirarin@nips.ac.jp.
The University of Tokyo · JPNational Institute for Physiological Sciences · JPThe Graduate University for Advanced Studies, SOKENDAI · JPJichi Medical University · JPShinshu University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regeneration of human kidneys in animal models would help combat the severe shortage of donors in transplantation therapy. Previously, we demonstrated by interspecific blastocyst complementation between mouse and rats, generation of pluripotent stem cell (PSC)-derived functional pancreas, in apancreatic Pdx1 mutant mice. We, however, were unable to obtain rat PSC-derived kidneys in anephric Sall1 mutant mice, likely due to the poor contribution of rat PSCs to the mouse metanephric mesenchyme, a nephron progenitor. Here, conversely, we show that mouse PSCs can efficiently differentiate into the metanephric mesenchyme in rat, allowing the generation of mouse PSC-derived kidney in anephric Sall1 mutant rat. Glomerular epithelium and renal tubules in the kidneys are entirely composed of mouse PSC-derived cells expressing key functional markers. Importantly, the ureter-bladder junction is normally formed. These data provide proof-of-principle for interspecific blastocyst complementation as a viable approach for kidney generation.

Indexed as

AnimalsBlastocystCell DifferentiationDisease Models, AnimalFemaleHomeodomain ProteinsHumansKidneyKidney Failure, ChronicMaleMesodermMiceMice, Inbred C57BLOrganogenesisPluripotent Stem CellsRatsHomeodomain Proteinspancreatic and duodenal homeobox 1 proteinSall1 protein, mouseTrans-ActivatorsTranscription Factors

Identifiers

PMID30723213
PMCPMC6363802
OpenAlexW2914840837

What OpenQuestion holds

Textmetadata
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.