Evidence map›Paper›PMID 39471483›Full record

ArticleBlood advances2025

Development of iPSC-derived human bone marrow organoid for autonomous hematopoiesis and patient-derived HSPC engraftment.

Kehan Ren, Ermin Li, Inci Aydemir, Yijie Liu, Xu Han, Honghao Bi, Pan Wang, Kara Tao, Amy Ji, Yi-Hua Chen and 3 more

Abstract read
In one paragraph

Article in Blood advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Artificial intelligence virtual bone organoids (AIVBOs).Journal of orthopaedic translation · 2026
    Review
  2. Article
  3. Article
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  5. Article
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  8. Stromal Gasdermin D-mediated Pyroptosis Drives Maladaptive CD4bioRxiv : the preprint server for biology · 2026
    Article
  9. Review
  10. Review
  11. Bridging skeletal stem cell diversity and human skeletal modeling.Journal of bone and mineral metabolism · 2026
    Review
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  13. 3DACS biomaterials science & engineering · 2026
    Review
  14. Review
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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.

Kehan RenDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL.ORCID 0000-0002-4409-7145
Ermin LiDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL.ORCID 0000-0002-0301-4155
Inci AydemirDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL.ORCID 0000-0002-6627-6080
Yijie LiuDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL.
Xu HanDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL.ORCID 0000-0002-9317-774X
Honghao BiDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL.
Pan WangDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL.
Kara TaoDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL.
Amy JiDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL.
Yi-Hua ChenDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL.
Jing YangDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL.
Madina SukhanovaDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL.
Peng JiDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL.ORCID 0000-0002-8849-3625

Funding

Targeting gasdermin D to treat myelodysplastic syndromesR01HL169507 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Peng Ji · 2023 to 2026
$2.1M
The roles of mDia2 in hematopoietic stem and progenitor cell engraftment and migrationR01HL148012 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI JI, PENG · 2020 to 2023
$2.1M
The roles of mDia2 in membrane remodeling and organelle clearance during reticulocyte formationR01DK124220 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI JI, PENG · 2020 to 2024
$2.0M
The role of Pleckstrin-2 as a functional node in myeloid proliferationR01HL150729 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI JI, PENG · 2020 to 2023
$2.0M
Functional roles of DDX41 in the homeostasis of G quadruplexes in erythropoiesisR01DK138205 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Peng Ji · 2024 to 2026
$1.4M
The functional role of DDX41 in myelodysplastic syndromesF32HL170648 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BI, HONGHAO · 2023 to 2025
$249k
The role of Gasdermin D in the bone marrow microenvironment during clonal hematopoiesis progressionK99CA289959 · NCI · NORTHWESTERN UNIVERSITY · PI REN, KEHAN · 2025 to 2025
$123k
NCI NIH HHS K99 CA289959NHLBI NIH HHS F32 HL170648NHLBI NIH HHS R01 HL148012NHLBI NIH HHS R01 HL150729NHLBI NIH HHS R01 HL169507NIDDK NIH HHS R01 DK124220NIDDK NIH HHS R01 DK138205
6 · The paper itself

Abstract

abstractCurrent efforts in translational studies in hematology often rely on immunodeficient mouse models for engrafting patient-derived hematopoietic stem and progenitor cells (HSPCs), yet these models often face challenges in effectively engrafting cells from patients with various diseases, such as myelodysplastic syndromes (MDSs). In this study, we developed an induced pluripotent stem cell (iPSC)-derived human bone marrow organoid model that closely replicates the bone marrow microenvironment, facilitating the engraftment of HSPCs derived from patients with MDS, thereby mirroring the patients' distinct disease characteristics. Specifically, using advanced microscopy, we verified the development of a complex 3-dimensional network of endothelial, stromal, and hematopoietic cells within organoids, resembling the autonomous human marrow microenvironment. Furthermore, we showed that HSPCs derived from the donor bone marrow of normal individuals or patients with MDS can migrate to and proliferate within the organoid vascular niche while maintaining self-renewal and original genetic profiles. Within the organoids, the differentiation patterns of MDS HSPCs were significantly distinct from those of multilineage hematopoiesis in normal HSPCs, which can be correlated with the clinical manifestations of the disease. These findings underscore the significance of the organoid model in studying human hematopoiesis and the pathophysiology of hematologic diseases, thereby offering new avenues for personalized medicine and therapeutic interventions.

Indexed as

HematopoiesisHematopoietic Stem CellsInduced Pluripotent Stem CellsOrganoidsAnimalsBone MarrowCell DifferentiationHematopoietic Stem Cell TransplantationHumansMiceMyelodysplastic Syndromes

Identifiers

PMID39471483
PMCPMC11732577

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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.