Evidence map›Paper›PMID 36483299›Full record

ReviewFrontiers in medical technology2022

Sourcing cells for

Molly C McCloskey, Victor Z Zhang, S Danial Ahmad, Samuel Walker, Samantha S Romanick, Hani A Awad, James L McGrath

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in medical technology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.6field-weighted citation impact, top 35% of its field
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

10 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
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  4. Review
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  9. 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

7 authors at 1 institution in 1 country.

Molly C McCloskeyDepartment of Biomedical Engineering, University of Rochester, Rochester, NY, United States.
Victor Z ZhangDepartment of Biomedical Engineering, University of Rochester, Rochester, NY, United States.
S Danial AhmadDepartment of Biomedical Engineering, University of Rochester, Rochester, NY, United States.
Samuel WalkerDepartment of Biomedical Engineering, University of Rochester, Rochester, NY, United States.
Samantha S RomanickDepartment of Biomedical Engineering, University of Rochester, Rochester, NY, United States.
Hani A AwadDepartment of Biomedical Engineering, University of Rochester, Rochester, NY, United States.
James L McGrathDepartment of Biomedical Engineering, University of Rochester, Rochester, NY, United States.
University of Rochester · US

Funding

VISUAL INDICES OF NEUROTOXICITYP30ES001247 · NIEHS · UNIVERSITY OF ROCHESTER · PI Martha Susiarjo · 1985 to 2026
$42.8M
University of Rochester Mentoring Environment: Nurturing Training Opportunities in Research (UR-MENTOR)T32GM007356 · NIGMS · UNIVERSITY OF ROCHESTER · PI O'BANION, M. KERRY · 1985 to 2023
$15.1M
MULTIDISCIPLINARY TRAINING IN PULMONARY RESEARCHT32HL066988 · NHLBI · UNIVERSITY OF ROCHESTER · PI GEORAS, STEVE N, O'REILLY, MICHAEL A · 2001 to 2021
$8.1M
The µSiM-hNVU - a human BBB platform for the study of brain injury mechanisms during systemic infectionR33HL154249 · NHLBI · UNIVERSITY OF ROCHESTER · PI ENGELHARDT, BRITTA, GABORSKI, THOMAS R · 2022 to 2024
$2.2M
A microphysiological system of tendon inflammation and fibrosis for drug screening and efficacy testing: MPS Database EngagementUG3TR003281 · NCATS · UNIVERSITY OF ROCHESTER · PI AWAD, HANI A, MCGRATH, JAMES L · 2020 to 2021
$1.6M
The µSiM-hNVU - a human BBB platform for the study of brain injury mechanisms during systemic infectionR61HL154249 · NHLBI · UNIVERSITY OF ROCHESTER · PI ENGELHARDT, BRITTA, GABORSKI, THOMAS R · 2020 to 2021
$1.2M
NCATS NIH HHS UG3 TR003281NHLBI NIH HHS R33 HL154249NHLBI NIH HHS R61 HL154249NHLBI NIH HHS T32 HL066988NIEHS NIH HHS P30 ES001247NIGMS NIH HHS T32 GM007356
6 · The paper itself

Abstract

The vascular system plays a critical role in the progression and resolution of inflammation. The contributions of the vascular endothelium to these processes, however, vary with tissue and disease state. Recently, tissue chip models have emerged as promising tools to understand human disease and for the development of personalized medicine approaches. Inclusion of a vascular component within these platforms is critical for properly evaluating most diseases, but many models to date use "generic" endothelial cells, which can preclude the identification of biomedically meaningful pathways and mechanisms. As the knowledge of vascular heterogeneity and immune cell trafficking throughout the body advances, tissue chip models should also advance to incorporate tissue-specific cells where possible. Here, we discuss the known heterogeneity of leukocyte trafficking in vascular beds of some commonly modeled tissues. We comment on the availability of different tissue-specific cell sources for endothelial cells and pericytes, with a focus on stem cell sources for the full realization of personalized medicine. We discuss sources available for the immune cells needed to model inflammatory processes and the findings of tissue chip models that have used the cells to studying transmigration.

Indexed as

endothelial cellinflammationmicrophysiological systemorgan-on-chippericytetissue chiptransmigrationvascular heterogeneity

Identifiers

PMID36483299
PMCPMC9724237
OpenAlexW4306964317

What OpenQuestion holds

Textmetadata
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.