Evidence map›Paper›PMID 42472629›Full record

ArticleStem cells translational medicine2026

Red blood cell differentiation using canine-induced pluripotent stem cells.

Kazuto Kimura, Masaya Tsukamoto, Kohei Shishida, Hiroko Sugisaki, Jun Katahira, Miyuu Tanaka, Mitsuru Kuwamura, Amir Kol, Mika Okada, Minoru Iijima and 3 more

Abstract read
In one paragraph

Article in Stem cells translational medicine, 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

13 authors.

Kazuto KimuraLaboratory of Cell Pathobiology, Department of Advanced Pathobiology, Graduate School of Veterinary Science, Osaka Metropolitan University, Izumisano, 598-8531, Japan.
Masaya TsukamotoLaboratory of Cell Pathobiology, Department of Advanced Pathobiology, Graduate School of Veterinary Science, Osaka Metropolitan University, Izumisano, 598-8531, Japan.
Kohei ShishidaLaboratory of Cell Pathobiology, Department of Advanced Pathobiology, Graduate School of Veterinary Science, Osaka Metropolitan University, Izumisano, 598-8531, Japan.
Hiroko SugisakiLaboratory of Cell Pathobiology, Department of Advanced Pathobiology, Graduate School of Veterinary Science, Osaka Metropolitan University, Izumisano, 598-8531, Japan.
Jun KatahiraLaboratory of Cellular Molecular Biology, Department of Integrated Functional Biosciences, Graduate School of Veterinary Science, Osaka Metropolitan University, Izumisano, 598-8531, Japan.ORCID 0000-0001-5188-0368
Miyuu TanakaLaboratory of Veterinary Pathology, Department of Integrated Structural Biosciences, Graduate School of Veterinary Science, Osaka Metropolitan University, Izumisano, 598-8531, Japan.
Mitsuru KuwamuraLaboratory of Veterinary Pathology, Department of Integrated Structural Biosciences, Graduate School of Veterinary Science, Osaka Metropolitan University, Izumisano, 598-8531, Japan.
Amir KolDepartment of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California, Davis, Davis, CA 95616, United States.
Mika OkadaTOKIWA-Bio Inc., Tsukuba, 305-0047, Japan.
Minoru IijimaTOKIWA-Bio Inc., Tsukuba, 305-0047, Japan.
Mahito NakanishiTOKIWA-Bio Inc., Tsukuba, 305-0047, Japan.
Kikuya SugiuraLaboratory of Cell Pathobiology, Department of Advanced Pathobiology, Graduate School of Veterinary Science, Osaka Metropolitan University, Izumisano, 598-8531, Japan.
Shingo HatoyaLaboratory of Cell Pathobiology, Department of Advanced Pathobiology, Graduate School of Veterinary Science, Osaka Metropolitan University, Izumisano, 598-8531, Japan.ORCID 0000-0001-5944-1394

Funding

JSPS KAKENHI 22H02525JSPS KAKENHI 22J14623JSPS KAKENHI 23K23790JSPS KAKENHI 26K01900JSPS KAKENHI JP18H02349
6 · The paper itself

Abstract

backgroundRed blood cell (RBC) transfusions are essential for treating various medical conditions, but global demand is difficult to meet due to a dwindling donor pool and compatibility issues. Pluripotent stem cells (PSCs) offer a promising alternative of blood dependent on volunteer donors for RBC production, and dogs serve as an excellent model for translational research due to their physiological and genetic similarities to humans.

methodsCanine induced pluripotent stem cells (ciPSCs) were differentiated toward hematopoietic and erythroid lineages. Differentiated cells were evaluated for hematopoietic marker expression, hemoglobinization, colony-forming capacity, enucleation, and hemoglobin gene expression. Glycophorin A (GYPA)-enhanced green fluorescent protein (EGFP) reporter ciPSC lines were generated using clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9-mediated genome editing to visualize GYPA expression during differentiation.

resultsThis study introduces a protocol for RBC differentiation using ciPSCs. We achieved generation of hemoglobinized RBCs, progressing through polychromatic and orthochromatic erythroblast-like stages. CiPSC-derived hematopoietic cells/RBCs were confirmed to have immature characteristics as determined by limited colony-forming capacities, low enucleation, and embryonic and fetal hemoglobin gene expression. Additionally, we created GYPA-EGFP reporter ciPSC lines using CRISPR-Cas9-mediated genome editing, enabling real-time visualization of GYPA expression. This innovation confirmed GYPA as a viable surface marker for ciPSC-derived RBCs.

conclusionOur findings mark an initial step toward establishing a canine PSC-based erythroid differentiation system, providing a foundation for future improvements and exploration of applications for canine PSC-derived RBCs.

Indexed as

Cell DifferentiationErythrocytesInduced Pluripotent Stem CellsAnimalsCRISPR-Cas SystemsDogsGlycophorinsGreen Fluorescent ProteinsGlycophorinsGreen Fluorescent Proteinscaninedifferentiationgenome editinginduced pluripotent stem cellsred blood cells

Identifiers

PMID42472629
PMCPMC13381058

What OpenQuestion holds

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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.