Evidence map›Paper›PMID 38838141›Full record

ArticleScience advances2024

An ultrathin membrane mediates tissue-specific morphogenesis and barrier function in a human kidney chip.

Xingrui Mou, Jessica Shah, Yasmin Roye, Carolyn Du, Samira Musah

Abstract read
In one paragraph

Article in Science advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Review
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  3. Organ-on-a-chip toxicology.Innovation (Cambridge (Mass.)) · 2026
    Review
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  7. Bridging the Gap Between Static Histology and Dynamic Organ-on-a-Chip Models.Pathophysiology : the official journal of the International Society for Pathophysiology · 2026
    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

5 authors.

Xingrui MouDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27710, USA.ORCID 0000-0002-4258-672X
Jessica ShahDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27710, USA.ORCID 0000-0002-0760-4232
Yasmin RoyeDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27710, USA.ORCID 0000-0002-4495-790X
Carolyn DuDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27710, USA.ORCID 0009-0004-4668-1259
Samira MusahDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27710, USA.ORCID 0000-0001-9432-6789

Funding

University of Michigan O'Brien Kidney Translational Core CenterP30DK081943 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PENNATHUR, SUBRAMANIAM · 2008 to 2022
$12.9M
TRIO NRSA Training CoreTL1DK139567 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Graca Duarte Almeida-Porada, Steven D Crowley · 2023 to 2026
$3.3M
U2C/TL1 NC KUH TRIO ProgramU2CDK133491 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Keisha L Gibson · 2023 to 2026
$2.4M
Harnessing stem cells and synthetic gene circuits to repair glomerular injuryDP2DK139544 · NIDDK · DUKE UNIVERSITY · PI Samira Musah · 2023 to 2026
$2.4M
NIDDK NIH HHS DP2 DK139544NIDDK NIH HHS P30 DK081943NIDDK NIH HHS TL1 DK139567NIDDK NIH HHS U2C DK133491
6 · The paper itself

Abstract

Organ-on-chip (OOC) systems are revolutionizing tissue engineering by providing dynamic models of tissue structure, organ-level function, and disease phenotypes using human cells. However, nonbiological components of OOC devices often limit the recapitulation of in vivo-like tissue-tissue cross-talk and morphogenesis. Here, we engineered a kidney glomerulus-on-a-chip that recapitulates glomerular morphogenesis and barrier function using a biomimetic ultrathin membrane and human-induced pluripotent stem cells. The resulting chip comprised a proximate epithelial-endothelial tissue interface, which reconstituted the selective molecular filtration function of healthy and diseased kidneys. In addition, fenestrated endothelium was successfully induced from human pluripotent stem cells in an OOC device, through in vivo-like paracrine signaling across the ultrathin membrane. Thus, this device provides a dynamic tissue engineering platform for modeling human kidney-specific morphogenesis and function, enabling mechanistic studies of stem cell differentiation, organ physiology, and pathophysiology.

Indexed as

KidneyLab-On-A-Chip DevicesMorphogenesisTissue EngineeringCell DifferentiationHumansInduced Pluripotent Stem CellsKidney GlomerulusMembranes, ArtificialMembranes, Artificial

Identifiers

PMID38838141
PMCPMC11152122

What OpenQuestion holds

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LicenceCC BY-NC
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.