Evidence map›Paper›PMID 42035221›Full record

ArticleStem cell research & therapy2026

Generation of functional mesothelial cells from human iPSCs that restore peritoneal integrity in experimental peritoneal injury.

Tadashi Kato, Mayu Yamashita, Masahiro Yasuda, Yutaro Ando, Ryusuke Nakatsuka, Yasumasa Shirouzu, Tatsuya Fujioka, Masayuki Tsukasaki, Fumiyuki Hattori, Yoshihiro Taniyama and 4 more

Abstract read
In one paragraph

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

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

14 authors.

Tadashi KatoDepartment of Medicine, Division of Nephrology, Showa Medical University Graduate School of Medicine, 1-5-8 Hatanodai, Shinagawa, Tokyo, 142-8555, Japan. t-k@med.showa-u.ac.jp.
Mayu YamashitaDepartment of Medicine, Division of Nephrology, Showa Medical University Graduate School of Medicine, 1-5-8 Hatanodai, Shinagawa, Tokyo, 142-8555, Japan.
Masahiro YasudaDepartment of iPS Stem Cell Regenerative Medicine, Kansai Medical University, Osaka, Japan.
Yutaro AndoDepartment of Biochemistry, School of Dentistry, Showa Medical University Graduate School of Medicine, Tokyo, Japan.
Ryusuke NakatsukaDepartment of Pharmacology, Faculty of Dentistry, Osaka Dental University, Osaka, Japan.
Yasumasa ShirouzuDepartment of iPS Stem Cell Regenerative Medicine, Kansai Medical University, Osaka, Japan.
Tatsuya FujiokaDepartment of iPS Stem Cell Regenerative Medicine, Kansai Medical University, Osaka, Japan.
Masayuki TsukasakiDepartment of Biochemistry, School of Dentistry, Showa Medical University Graduate School of Medicine, Tokyo, Japan.
Fumiyuki HattoriDepartment of iPS Stem Cell Regenerative Medicine, Kansai Medical University, Osaka, Japan.
Yoshihiro TaniyamaDepartment of Medicine II, Kansai Medical University, Osaka, Japan.
Hiroaki OgataDepartment of Medicine, Division of Nephrology, Showa Medical University Graduate School of Medicine, 1-5-8 Hatanodai, Shinagawa, Tokyo, 142-8555, Japan.
Akiko SakashitaDepartment of Medicine, Division of Hematology, Showa Medical University Graduate School of Medicine, Tokyo, Japan.
Hirokazu HondaDepartment of Medicine, Division of Nephrology, Showa Medical University Graduate School of Medicine, 1-5-8 Hatanodai, Shinagawa, Tokyo, 142-8555, Japan.
Hirofumi HitomiDepartment of iPS Stem Cell Regenerative Medicine, Kansai Medical University, Osaka, Japan.

Funding

Japan Society for the Promotion of Science 20K08598Japan Society for the Promotion of Science 21K08292Japan Society for the Promotion of Science 25K11550
6 · The paper itself

Abstract

backgroundLong-term peritoneal injury results in loss of mesothelial integrity and impaired ultrafiltration, limiting the durability of peritoneal dialysis. Because primary human peritoneal mesothelial cells (PMCs) are difficult to obtain and expand, regenerative strategies for restoring peritoneal function have remained limited.

methodsWe developed a protocol to differentiate human induced pluripotent stem cells (iPSCs) into functional peritoneal mesothelial-like cells (iPMCs). The molecular and functional characteristics of iPMCs were evaluated using gene expression analyses and functional assays, including comparison with a mesothelial cell model. The therapeutic effect of iPMCs was evaluated in a methylglyoxal-induced experimental peritoneal injury mouse model.

resultsiPMCs exhibited typical cobblestone morphology and expressed key mesothelial markers including CK18, WT1 and MSLN. Transcriptomic analysis demonstrated strong similarity between iPMCs and primary PMCs. In vivo, intraperitoneal administration of iPMCs partially improved peritoneal transport parameters in a mouse model of peritoneal injury.

conclusionsWe successfully generated functional mesothelial cells from human iPSCs that reproduce mesothelial-like functional properties and suggest potential for restoring peritoneal integrity. This study demonstrates the feasibility of iPSC-derived mesothelial cells as a regenerative cell source for peritoneal repair and provides a foundation for future peritoneal regeneration therapy.

Indexed as

Epithelial CellsInduced Pluripotent Stem CellsPeritoneumAnimalsCell DifferentiationDisease Models, AnimalEpitheliumHumansMaleMicePeritoneal DialysisInduced pluripotent stem cellsPeritoneal dialysisPeritoneal mesothelial cellsPermeabilityWound healing

Identifiers

PMID42035221
PMCPMC13255358

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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.