Evidence map›Paper›PMID 34118217›Full record

ReviewJournal of molecular and cellular cardiology2021

Organ-on-a-chip systems for vascular biology.

Christian J Mandrycky, Caitlin C Howard, Samuel G Rayner, Yu Jung Shin, Ying Zheng

Abstract readReview
In one paragraph

Review in Journal of molecular and cellular cardiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing 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

51 citing papers in PubMed.

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  11. The importance of mechanical forces in chronic respiratory diseases.European respiratory review : an official journal of the European Respiratory Society · 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.

Christian J MandryckyDepartment of Bioengineering, University of Washington, 3720 15th Ave NE, Seattle, WA 98105, USA. Electronic address: cmandryc@uw.edu.
Caitlin C HowardDepartment of Bioengineering, University of Washington, 3720 15th Ave NE, Seattle, WA 98105, USA. Electronic address: cchoward@uw.edu.
Samuel G RaynerDepartment of Bioengineering, University of Washington, 3720 15th Ave NE, Seattle, WA 98105, USA; Department of Medicine; Division of Pulmonary, Critical Care and Sleep Medicine, University of Washington, Seattle, WA 98195, USA. Electronic address: srayner@uw.edu.
Yu Jung ShinDepartment of Bioengineering, University of Washington, 3720 15th Ave NE, Seattle, WA 98105, USA. Electronic address: yshin20@uw.edu.
Ying ZhengDepartment of Bioengineering, University of Washington, 3720 15th Ave NE, Seattle, WA 98105, USA; Institute for Stem Cell and Regenerative Medicine, Seattle, WA 98195, USA. Electronic address: yingzy@uw.edu.

Funding

Mechanisms of endothelial dysfunction in cerebral malaria and barrier restorative pathwaysR01AI148802 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI SMITH, JOSEPH D · 2020 to 2024
$3.5M
Perfusable 3D human cardiac constructs for heart regenerationR01HL141570 · NHLBI · UNIVERSITY OF WASHINGTON · PI MURRY, CHARLES E, ZHENG, YING · 2018 to 2021
$3.3M
Molecular Mechanisms in Pediatric Cerebral Malaria Pathogenesis and ImmunityR01AI141602 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI SEYDEL, KARL BOYNTON, SMITH, JOSEPH D · 2019 to 2022
$2.9M
Rebuilding the glomerular filtration barrier by regenerating adult podocytesUH3DK107343 · NIDDK · UNIVERSITY OF WASHINGTON · PI SHANKLAND, STUART JAMES, ZHENG, YING · 2017 to 2019
$1.3M
Rebuilding the glomerular filtration barrier by regenerating adult podocytesUH2DK107343 · NIDDK · UNIVERSITY OF WASHINGTON · PI SHANKLAND, STUART JAMES, ZHENG, YING · 2015 to 2016
$855k
Modeling Von Willebrand Factor Behavior in the Pulmonary Circulation in Health and DiseaseF32HL143949 · NHLBI · UNIVERSITY OF WASHINGTON · PI RAYNER, SAMUEL GIBSON · 2018 to 2019
$112k
NHLBI NIH HHS F32 HL143949NHLBI NIH HHS R01 HL141570NIAID NIH HHS R01 AI141602NIAID NIH HHS R01 AI148802NIDDK NIH HHS UH2 DK107343NIDDK NIH HHS UH3 DK107343
6 · The paper itself

Abstract

Organ-on-a-chip (OOC) platforms involve the miniaturization of cell culture systems and enable a variety of novel experimental approaches. These range from modeling the independent effects of biophysical forces on cells to screening novel drugs in multi-organ microphysiological systems, all within microscale devices. As in living systems, the incorporation of vascular structure is a key feature common to almost all organ-on-a-chip systems. In this review we highlight recent advances in organ-on-a-chip technologies with a focus on the vasculature. We first present the developmental process of the blood vessels through which vascular cells assemble into networks and remodel to form complex vascular beds under flow. We then review self-assembled vascular models and flow systems for the study of vascular development and biology as well as pre-patterned vascular models for the generation of perfusable microvessels for modeling vascular and tissue function. We finally conclude with a perspective on developing future OOC approaches for studying different aspects of vascular biology. We highlight the fit for purpose selection of OOC models towards either simple but powerful testbeds for therapeutic development, or complex vasculature to accurately replicate human physiology for specific disease modeling and tissue regeneration.

Indexed as

AnimalsBiologyBlood VesselsGuided Tissue RegenerationHumansLab-On-A-Chip DevicesEndothelial cellsMechanotransductionMicrofluidicsOrganoidsOrgan-on-a-chipVascular biology

Identifiers

PMID34118217
PMCPMC8545919

What OpenQuestion holds

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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.