Evidence map›Paper›PMID 24676392›Full record

ArticleIntegrative biology : quantitative biosciences from nano to macro2014

Generation of 3D functional microvascular networks with human mesenchymal stem cells in microfluidic systems.

Jessie S Jeon, Simone Bersini, Jordan A Whisler, Michelle B Chen, Gabriele Dubini, Joseph L Charest, Matteo Moretti, Roger D Kamm

Open access · greenAbstract read
In one paragraph

Article in Integrative biology : quantitative biosciences from nano to macro, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 128 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
128citing papers in PubMed, 1 pooled it
9.6field-weighted citation impact, top 1% 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

128 citing papers in PubMed, 1 synthesis or guideline pooled it, 229 citations in OpenAlex.

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  15. A Cell Pre-Wrapping Seeding Technique for Hydrogel-Based Tubular Organ-On-A-Chip.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
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68 more citing papers are in PubMed but not listed here.

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

8 authors at 5 institutions in 2 countries.

Jessie S JeonDepartment of Mechanical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA, USA 02139. rdkamm@mit.edu.
Simone Bersini
Jordan A Whisler
Michelle B Chen
Gabriele Dubini
Joseph L Charest
Matteo Moretti
Roger D Kamm
Massachusetts Institute of Technology · USDraper Laboratory · USIstituti di Ricovero e Cura a Carattere Scientifico · ITIstituto Ortopedico Galeazzi · ITPolitecnico di Milano · IT

Funding

Microfluidic 3D Assays for Metastatic CancerR33CA174550 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI KAMM, ROGER D · 2013 to 2015
$1.1M
Microfluidic 3D Scaffold Assay for Cancer Cell Migration and IntravasationR21CA140096 · NCI · CHARLES STARK DRAPER LABORATORY · PI CHAREST, JOSEPH L. · 2009 to 2011
$672k
NCI NIH HHS R21 CA140096NCI NIH HHS R33 CA174550NCI NIH HHS R33 CA174550-01
6 · The paper itself

Abstract

The generation of functional microvascular networks is critical for the development of advanced in vitro models to replicate pathophysiological conditions. Mural cells provide structural support to blood vessels and secrete biomolecules contributing to vessel stability and functionality. We investigated the role played by two endothelium-related molecules, angiopoietin (Ang-1) and transforming growth factor (TGF-β1), on bone marrow-derived human mesenchymal stem cell (BM-hMSC) phenotypic transition toward a mural cell lineage, both in monoculture and in direct contact with human endothelial cells (ECs), within 3D fibrin gels in microfluidic devices. We demonstrated that the effect of these molecules is dependent on direct heterotypic cell-cell contact. Moreover, we found a significant increase in the amount of α-smooth muscle actin in microvascular networks with added VEGF and TGF-β1 or VEGF and Ang-1 compared to networks with added VEGF alone. However, the addition of TGF-β1 generated a non-interconnected microvasculature, while Ang-1 promoted functional networks, confirmed by microsphere perfusion and permeability measurements. The presence of mural cell-like BM-hMSCs coupled with the addition of Ang-1 increased the number of network branches and reduced mean vessel diameter compared to EC only vasculature. This system has promising applications in the development of advanced in vitro models to study complex biological phenomena involving functional and perfusable microvascular networks.

Indexed as

Angiopoietin-1Cell DifferentiationCell LineageCoculture TechniquesEndothelial CellsHumansMesenchymal Stem CellsMicrofluidicsMicroscopy, ConfocalMicrovesselsTransforming Growth Factor beta1Vascular Endothelial Growth Factor AAngiopoietin-1ANGPT1 protein, humanTransforming Growth Factor beta1Vascular Endothelial Growth Factor AVEGFA protein, human

Identifiers

PMID24676392
PMCPMC4307755
OpenAlexW2050384796

What OpenQuestion holds

Textmetadata
LicenceTDM
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.