Evidence map›Paper›PMID 31752157›Full record

ArticleCells2019

Natural Histogel-Based Bio-Scaffolds for Sustaining Angiogenesis in Beige Adipose Tissue.

Margherita Di Somma, Wandert Schaafsma, Elisabetta Grillo, Maria Vliora, Eleni Dakou, Michela Corsini, Cosetta Ravelli, Roberto Ronca, Paraskevi Sakellariou, Jef Vanparijs and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

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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

12 authors at 3 institutions in 3 countries.

Margherita Di SommaDepartment of Molecular and Translational Medicine, University of Brescia, 25121 Brescia, Italy.
Wandert SchaafsmaHistocell, S.L.Parque Tecnológico 801A, 2o 48160 Derio-BIZKAIA, Spain.
Elisabetta GrilloDepartment of Molecular and Translational Medicine, University of Brescia, 25121 Brescia, Italy.ORCID 0000-0002-8403-0607
Maria VlioraDepartment of Molecular and Translational Medicine, University of Brescia, 25121 Brescia, Italy.ORCID 0000-0002-1884-1057
Eleni DakouLaboratory of Cell Genetics, Department of Biology, Faculty of Science and Bioengineering Sciences, Vrije Universiteit Brussel, 1050 Brussels, Belgium.ORCID 0000-0001-7277-4345
Michela CorsiniDepartment of Molecular and Translational Medicine, University of Brescia, 25121 Brescia, Italy.ORCID 0000-0002-8673-4376
Cosetta RavelliDepartment of Molecular and Translational Medicine, University of Brescia, 25121 Brescia, Italy.
Roberto RoncaDepartment of Molecular and Translational Medicine, University of Brescia, 25121 Brescia, Italy.ORCID 0000-0001-8979-7068
Paraskevi SakellariouFAME Laboratory, Department of Exercise Science, University of Thessaly, 38221 Trikala, Greece.
Jef VanparijsDepartment of Human Physiology, Faculty of Physical Education and Physical Therapy, Vrije Universiteit Brussel, 1050 Brussels, Belgium.
Begona CastroHistocell, S.L.Parque Tecnológico 801A, 2o 48160 Derio-BIZKAIA, Spain.
Stefania MitolaDepartment of Molecular and Translational Medicine, University of Brescia, 25121 Brescia, Italy.
University of Brescia · ITUniversity of Thessaly · GRVrije Universiteit Brussel · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the treatment of obesity and its related disorders, one of the measures adopted is weight reduction by controlling nutrition and increasing physical activity. A valid alternative to restore the physiological function of the human body could be the increase of energy consumption by inducing the browning of adipose tissue. To this purpose, we tested the ability of Histogel, a natural mixture of glycosaminoglycans isolated from animal Wharton jelly, to sustain the differentiation of adipose derived mesenchymal cells (ADSCs) into brown-like cells expressing UCP-1. Differentiated cells show a higher energy metabolism compared to undifferentiated mesenchymal cells. Furthermore, Histogel acts as a pro-angiogenic matrix, induces endothelial cell proliferation and sprouting in a three-dimensional gel in vitro, and stimulates neovascularization when applied in vivo on top of the chicken embryo chorioallantoic membrane or injected subcutaneously in mice. In addition to the pro-angiogenic activity of Histogel, also the ADSC derived beige cells contribute to activating endothelial cells. These data led us to propose Histogel as a promising scaffold for the modulation of the thermogenic behavior of adipose tissue. Indeed, Histogel simultaneously supports the acquisition of brown tissue markers and activates the vasculature process necessary for the correct function of the thermogenic tissue. Thus, Histogel represents a valid candidate for the development of bioscaffolds to increase the amount of brown adipose tissue in patients with metabolic disorders.

Indexed as

Adipose Tissue, BeigeAnimalsCell DifferentiationCell ProliferationCells, CulturedChick EmbryoEnergy MetabolismGlycosaminoglycansHumansMesenchymal Stem CellsMiceNeovascularization, PhysiologicThermogenesisTissue ScaffoldsWharton JellyGlycosaminoglycansadipose derived mesenchymal cellsangiogenesisHistogel

Identifiers

PMID31752157
PMCPMC6912328
OpenAlexW2988182544

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.