Evidence map›Paper›PMID 35087424›Full record

ArticleFrontiers in physiology2021

Endothelial Cells Promote Osteogenesis by Establishing a Functional and Metabolic Coupling With Human Mesenchymal Stem Cells.

Sara Petrillo, Tullio Genova, Giorgia Chinigò, Ilaria Roato, Giorgia Scarpellino, Joanna Kopecka, Fiorella Altruda, Emanuela Tolosano, Chiara Riganti, Federico Mussano and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

10 citing papers in PubMed, 14 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

11 authors at 1 institution in 1 country.

Sara PetrilloMolecular Biotechnology Center (MBC), Department of Molecular Biotechnology and Health Sciences, University of Turin, Turin, Italy.
Tullio GenovaDepartment of Life Sciences and Systems Biology, University of Turin, Turin, Italy.
Giorgia ChinigòDepartment of Life Sciences and Systems Biology, University of Turin, Turin, Italy.
Ilaria RoatoDepartment of Surgical Sciences, C.I.R. Dental School, University of Turin, Turin, Italy.
Giorgia ScarpellinoDepartment of Life Sciences and Systems Biology, University of Turin, Turin, Italy.
Joanna KopeckaDepartment of Oncology, University of Turin, Turin, Italy.
Fiorella AltrudaMolecular Biotechnology Center (MBC), Department of Molecular Biotechnology and Health Sciences, University of Turin, Turin, Italy.
Emanuela TolosanoMolecular Biotechnology Center (MBC), Department of Molecular Biotechnology and Health Sciences, University of Turin, Turin, Italy.
Chiara RigantiDepartment of Oncology, University of Turin, Turin, Italy.
Federico MussanoDepartment of Surgical Sciences, C.I.R. Dental School, University of Turin, Turin, Italy.
Luca MunaronDepartment of Life Sciences and Systems Biology, University of Turin, Turin, Italy.
University of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone formation involves a complex crosstalk between endothelial cells (EC) and osteodifferentiating stem cells. This functional interplay is greatly mediated by the paracrine and autocrine action of soluble factors released at the vasculature-bone interface. This study elucidates the molecular and functional responses triggered by this intimate interaction. In this study, we showed that human dermal microvascular endothelial cells (HMEC) induced the expression of pro-angiogenic factors in stem cells from human exfoliated deciduous teeth (SHED) and sustain their osteo-differentiation at the same time. In contrast, osteodifferentiating SHED increased EC recruitment and promoted the formation of complex vascular networks. Moreover, HMEC enhanced anaerobic glycolysis in proliferating SHED without compromising their ability to undergo the oxidative metabolic shift required for adequate osteo-differentiation. Taken together, these findings provide novel insights into the molecular mechanism underlying the synergistic cooperation between EC and stem cells during bone tissue renewal.

Indexed as

bone biologybone regenerationendothelial cell (EC)HMECmesenchymal stem cell (MSC)metabolismosteogenesis

Identifiers

PMID35087424
PMCPMC8787057
OpenAlexW4206655305

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.