Evidence map›Paper›PMID 36443378›Full record

ArticleScientific reports2022

Organotypic stromal cells impact endothelial cell transcriptome in 3D microvessel networks.

Matthew B Curtis, Natalie Kelly, Christopher C W Hughes, Steven C George

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Bioengineering vascularization.Development (Cambridge, England) · 2024
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Mammary Microvessels are Sensitive to Menstrual Cycle Sex Hormones.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  12. Review
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

4 authors at 2 institutions in 1 country.

Matthew B CurtisDepartment of Biomedical Engineering, University of California, Davis, 451 E. Health Sciences Drive, Room 2315, Davis, CA, 95616, USA.ORCID 0000-0002-6796-9700
Natalie KellyDepartment of Biomedical Engineering, University of California, Davis, 451 E. Health Sciences Drive, Room 2315, Davis, CA, 95616, USA.
Christopher C W HughesDepartment of Biomedical Engineering, University of California Irvine, Irvine, CA, USA.ORCID 0000-0002-3223-830X
Steven C GeorgeDepartment of Biomedical Engineering, University of California, Davis, 451 E. Health Sciences Drive, Room 2315, Davis, CA, 95616, USA. scgeorge@ucdavis.edu.ORCID 0000-0003-2263-1914
University of California, Davis · USUniversity of California, Irvine · US

Funding

A 3D IN VITRO DISEASE MODEL OF ATRIAL CONDUCTIONUH3HL141800 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CURIEL, DAVID TERRY, GEORGE, STEVEN CARL · 2019 to 2021
$4.0M
A 3D IN VITRO DISEASE MODEL OF ATRIAL CONDUCTIONUG3HL141800 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CURIEL, DAVID TERRY, GEORGE, STEVEN CARL · 2017 to 2018
$2.6M
NHLBI NIH HHS UG3 HL141800NHLBI NIH HHS UH3 HL141800NIH HHS UH3 HL141800
6 · The paper itself

Abstract

Endothelial cells line all major blood vessels and serve as integral regulators of many functions including vessel diameter, cellular trafficking, and transport of soluble mediators. Despite similar functions, the phenotype of endothelial cells is highly organ-specific, yet our understanding of the mechanisms leading to organ-level differentiation is incomplete. We generated 3D microvessel networks by combining a common naïve endothelial cell with six different stromal cells derived from the lung, skin, heart, bone marrow, pancreas, and pancreatic cancer. Single cell RNA-Seq analysis of the microvessel networks reveals five distinct endothelial cell populations, for which the relative proportion depends on the stromal cell population. Morphologic features of the organotypic vessel networks inversely correlate with a cluster of endothelial cells associated with protein synthesis. The organotypic stromal cells were each characterized by a unique subpopulation of cells dedicated to extracellular matrix organization and assembly. Finally, compared to cells in 2D monolayer, the endothelial cell transcriptome from the 3D in vitro heart, skin, lung, and pancreas microvessel networks are more similar to the in vivo endothelial cells from the respective organs. We conclude that stromal cells contribute to endothelial cell and microvessel network organ tropism, and create an endothelial cell phenotype that more closely resembles that present in vivo.

Indexed as

Endothelial CellsPancreatic NeoplasmsHumansMicrovesselsStromal CellsTranscriptome

Identifiers

PMID36443378
PMCPMC9705391
OpenAlexW4310197887

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.