Evidence map›Paper›PMID 36498931›Full record

ArticleInternational journal of molecular sciences2022

Spatial-Controlled Coating of Pro-Angiogenic Proteins on 3D Porous Hydrogels Guides Endothelial Cell Behavior.

Chau Le Bao, Helen Waller, Alessandra Dellaquila, Daniel Peters, Jeremy Lakey, Frédéric Chaubet, Teresa Simon-Yarza

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 39% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Cell-Material Interactions 2022.International journal of molecular sciences · 2023
    Article
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 2 institutions in 2 countries.

Chau Le BaoLaboratory for Vascular Translational Science (LVTS) INSERM U1148, Université Paris Cité, Université Sorbonne Paris Nord, CEDEX 18, 75877 Paris, France.ORCID 0000-0002-1242-5394
Helen WallerBiosciences Institute, Newcastle University Biosciences Institute, Newcastle upon Tyne NE1 7RU, UK.ORCID 0000-0002-9608-3896
Alessandra DellaquilaLaboratory for Vascular Translational Science (LVTS) INSERM U1148, Université Paris Cité, Université Sorbonne Paris Nord, CEDEX 18, 75877 Paris, France.
Daniel PetersBiosciences Institute, Newcastle University Biosciences Institute, Newcastle upon Tyne NE1 7RU, UK.
Jeremy LakeyBiosciences Institute, Newcastle University Biosciences Institute, Newcastle upon Tyne NE1 7RU, UK.ORCID 0000-0003-4646-9085
Frédéric ChaubetLaboratory for Vascular Translational Science (LVTS) INSERM U1148, Université Paris Cité, Université Sorbonne Paris Nord, CEDEX 18, 75877 Paris, France.ORCID 0000-0001-7375-0425
Teresa Simon-YarzaLaboratory for Vascular Translational Science (LVTS) INSERM U1148, Université Paris Cité, Université Sorbonne Paris Nord, CEDEX 18, 75877 Paris, France.ORCID 0000-0002-2678-0776
Inserm · FRNewcastle University · GB

Funding

French Research Agency ANR under the project "DILI-on-chip" ANR-20-CE18-0001French Research Agency ANR under the project "EXCALYBUR" ANR-20-CE18-0001-01French Research Agency ANR under the project "iLite" ANR-16-RHUS-0005Université Paris Cité IDEX UP AAP EMERGENCE SIMON
6 · The paper itself

Abstract

In tissue engineering, the composition and the structural arrangement of molecular components within the extracellular matrix (ECM) determine the physical and biochemical features of a scaffold, which consequently modulate cell behavior and function. The microenvironment of the ECM plays a fundamental role in regulating angiogenesis. Numerous strategies in tissue engineering have attempted to control the spatial cues mimicking in vivo angiogenesis by using simplified systems. The aim of this study was to develop 3D porous crosslinked hydrogels with different spatial presentation of pro-angiogenic molecules to guide endothelial cell (EC) behavior. Hydrogels with pores and preformed microchannels were made with pharmaceutical-grade pullulan and dextran and functionalized with novel pro-angiogenic protein polymers (Caf1-YIGSR and Caf1-VEGF). Hydrogel functionalization was achieved by electrostatic interactions via incorporation of diethylaminoethyl (DEAE)-dextran. Spatial-controlled coating of hydrogels was realized through a combination of freeze-drying and physical absorption with Caf1 molecules. Cells in functionalized scaffolds survived, adhered, and proliferated over seven days. When incorporated alone, Caf1-YIGSR mainly induced cell adhesion and proliferation, whereas Caf1-VEGF promoted cell migration and sprouting. Most importantly, directed cell migration required the presence of both proteins in the microchannel and in the pores, highlighting the need for an adhesive substrate provided by Caf1-YIGSR for Caf1-VEGF to be effective. This study demonstrates the ability to guide EC behavior through spatial control of pro-angiogenic cues for the study of pro-angiogenic signals in 3D and to develop pro-angiogenic implantable materials.

Indexed as

Angiogenic ProteinsVascular Endothelial Growth Factor ABiocompatible MaterialsDextransEndothelial CellsHydrogelsAngiogenic ProteinsBiocompatible MaterialsDextransHydrogelsVascular Endothelial Growth Factor Aangiogenesiselectrostatic interactionshydrogelsspatial-controlled coatingtissue engineering

Identifiers

PMID36498931
PMCPMC9737628
OpenAlexW4310036607

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.