Evidence map›Paper›PMID 31944591›Full record

ArticleAdvanced healthcare materials2020

Distinguishing Specific CXCL12 Isoforms on Their Angiogenesis and Vascular Permeability Promoting Properties.

Chia-Wen Chang, Alex J Seibel, Alex Avendano, Marcos G Cortes-Medina, Jonathan W Song

Abstract read
In one paragraph

Article in Advanced healthcare materials, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

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  16. The mechanics of fibrillar collagen extracellular matrix.Cell reports. Physical science · 2021
    Article
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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.

Chia-Wen ChangDepartment of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, OH, 43210, USA.ORCID 0000-0002-0810-8556
Alex J SeibelDepartment of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, OH, 43210, USA.
Alex AvendanoDepartment of Biomedical Engineering, The Ohio State University, Columbus, OH, 43210, USA.ORCID 0000-0003-0528-8392
Marcos G Cortes-MedinaDepartment of Biomedical Engineering, The Ohio State University, Columbus, OH, 43210, USA.
Jonathan W SongDepartment of Mechanical and Aerospace Engineering, The Ohio State University, Columbus, OH, 43210, USA.ORCID 0000-0002-6991-5298

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Jennifer A. Woyach · 1985 to 2026
$132.3M
Biophysical-based approach for controlling blood vessel structure and functionR01HL141941 · NHLBI · OHIO STATE UNIVERSITY · PI CASTRO, CARLOS E., PRAKASH, SHAURYA · 2018 to 2021
$2.0M
NCI NIH HHS P30 CA016058NHLBI NIH HHS R01 HL141941
6 · The paper itself

Abstract

Angiogenesis is associated with increased vessel sprouting and permeability. Important mediators of these angiogenic responses include local environment of signaling molecules and supporting extracellular matrix (ECM). However, dissecting the interplay of these instructive signals in vivo with multiple cells and extracellular molecules remains a central challenge. Here, microfluidic biomimicry is integrated with 3D ECM hydrogels that are well-characterized for molecular-binding and mechanical properties to reconstitute vessel-like analogues in vitro. This study focuses on three distinct isoforms of the pro-metastatic chemokine CXCL12. In collagen-only hydrogel, CXCL12-α is the most potent isoform in promoting sprouting and permeability, followed by CXCL12-β and CXCL12-γ. Strikingly, addition of hyaluronan (HA), a large and negatively charged glycosaminoglycan, with collagen matrices selectively increases vessel sprouting and permeability conferred by CXCL12-γ. This outcome is supported by the measured binding affinities to collagen/HA ECM, suggesting that negatively charged HA increases the binding of CXCL12-γ to augment its angiogenic potency. Moreover, it is shown that addition of HA to collagen matrices on its own decreases vessel sprouting and permeability, and these responses are nullified by blocking the HA receptor CD44. Collectively, these results demonstrate that differences in binding to extracellular HA help underlie CXCL12 isoform-specific responses toward directing angiogenesis.

Indexed as

Capillary PermeabilityChemokine CXCL12CollagenExtracellular MatrixHumansHyaluronic AcidProtein IsoformsChemokine CXCL12CollagenHyaluronic AcidProtein Isoformschemokineextracellular matrixhyaluronic acidmatrix-bound ligandsmicrofluidicsmicrovessel analoguesvascular function

Identifiers

PMID31944591
PMCPMC7033017

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Registered trials

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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.