Evidence map›Paper›PMID 42276057›Full record

ArticleStem cell reports2026

Rat cell-derived kidney generation via interspecies blastocyst complementation in an Osr1-KO mouse model.

Shunsuke Yuri, Ayako Isotani

Abstract read
In one paragraph

Article in Stem cell reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Shunsuke YuriLaboratory of Experimental Animals, Research Institution, National Center for Geriatrics and Gerontology, 7-430 Morioka-cho, Obu, Aichi 474-8511, Japan; Division of Biological Science, Graduate School of Science and Technology, Nara Institute of Science and Technology, 8916-5 Takayama-cho, Ikoma, Nara 630-0192, Japan. Electronic address: shunsukeyuri@ncgg.go.jp.
Ayako IsotaniDivision of Biological Science, Graduate School of Science and Technology, Nara Institute of Science and Technology, 8916-5 Takayama-cho, Ikoma, Nara 630-0192, Japan; Life Science Collaboration Center (LiSCo), Nara Institute of Science and Technology, 8916-5 Takayama-cho, Ikoma, Nara 630-0192, Japan. Electronic address: isotani@bs.naist.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interspecies blastocyst complementation (BC) provides a promising approach to generate transplantable organs from pluripotent stem cells (PSCs). However, interspecies kidney generation has remained largely unsuccessful, particularly when using rat PSCs in mouse hosts. Here, we investigated multiple renal-deficient models (Sall1-, Ret-, and Osr1-knockouts [KOs]) through reverse BC (rBC) analyses. We identified Osr1-KO embryos as lacking both nephron progenitor and ureteric bud lineages, providing a vacant developmental niche for renal reconstruction. Injection of rat embryonic stem cells (ESCs) into Osr1-KO mouse blastocysts led to robust rat cell contribution and the formation of kidneys predominantly composed of rat in the vacant niche. These findings establish the Osr1-KO model as a permissive platform for interspecies kidney organogenesis and offer mechanistic insight into developmental compatibility underlying xenogeneic organ generation.

Indexed as

BlastocystKidneyTranscription FactorsAnimalsCell DifferentiationEmbryonic Stem CellsFemaleMiceMice, KnockoutOrganogenesisRatsTranscription Factorsblastocyst complementationinterspecies chimerakidney developmentkidney regeneration

Identifiers

PMID42276057
PMCPMC13385422

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Registered trials

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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.