Evidence map›Paper›PMID 36805780›Full record

ArticleStem cell research & therapy2023

Flow-dependent shear stress affects the biological properties of pericyte-like cells isolated from human dental pulp.

Giulia Bertani, Rosanna Di Tinco, Laura Bertoni, Giulia Orlandi, Alessandra Pisciotta, Roberto Rosa, Luca Rigamonti, Michele Signore, Jessika Bertacchini, Paola Sena and 3 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

14 citing papers in PubMed, 18 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

13 authors at 2 institutions in 1 country.

Giulia Bertani *Department of Surgery, Medicine Dentistry and Morphological Sciences With Interest in Transplant, University of Modena and Reggio Emilia, Modena, Italy.
Rosanna Di Tinco *Department of Surgery, Medicine Dentistry and Morphological Sciences With Interest in Transplant, University of Modena and Reggio Emilia, Modena, Italy.
Laura Bertoni *Department of Surgery, Medicine Dentistry and Morphological Sciences With Interest in Transplant, University of Modena and Reggio Emilia, Modena, Italy.
Giulia OrlandiDepartment of Surgery, Medicine Dentistry and Morphological Sciences With Interest in Transplant, University of Modena and Reggio Emilia, Modena, Italy.
Alessandra PisciottaDepartment of Surgery, Medicine Dentistry and Morphological Sciences With Interest in Transplant, University of Modena and Reggio Emilia, Modena, Italy.
Roberto RosaDepartment of Engineering Sciences and Methods, University of Modena and Reggio Emilia, Modena, Italy.
Luca RigamontiDepartment of Chemical and Geological Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Michele SignoreRPPA Unit, Proteomics Area, Core Facilities, Istituto Superiore di Sanità, Rome, Italy.
Jessika BertacchiniDepartment of Surgery, Medicine Dentistry and Morphological Sciences With Interest in Transplant, University of Modena and Reggio Emilia, Modena, Italy.
Paola SenaDepartment of Surgery, Medicine Dentistry and Morphological Sciences With Interest in Transplant, University of Modena and Reggio Emilia, Modena, Italy.
Sara De BiasiDepartment of Medical and Surgical Sciences for Children and Adults, University of Modena and Reggio Emilia, Modena, Italy.
Erica Villa *Department of Surgery, Medicine Dentistry and Morphological Sciences With Interest in Transplant, University of Modena and Reggio Emilia, Modena, Italy.
Gianluca Carnevale *Department of Surgery, Medicine Dentistry and Morphological Sciences With Interest in Transplant, University of Modena and Reggio Emilia, Modena, Italy. gianluca.carnevale@unimore.it.ORCID 0000-0002-5348-5991
University of Modena and Reggio Emilia · ITIstituto Superiore di Sanità · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHuman dental pulp stem cells represent a mesenchymal stem cell niche localized in the perivascular area of dental pulp and are characterized by low immunogenicity and immunomodulatory/anti-inflammatory properties. Pericytes, mural cells surrounding the endothelium of small vessels, regulate numerous functions including vessel growth, stabilization and permeability. It is well established that pericytes have a tight cross talk with endothelial cells in neoangiogenesis and vessel stabilization, which are regulated by different factors, i.e., microenvironment and flow-dependent shear stress. The aim of this study was to evaluate the effects of a pulsatile unidirectional flow in the presence or not of an inflammatory microenvironment on the biological properties of pericyte-like cells isolated from human dental pulp (hDPSCs).

methodsHuman DPSCs were cultured under both static and dynamic conditions with or without pre-activated peripheral blood mononuclear cells (PBMCs). Pulsatile unidirectional flow shear stress was generated by using a specific peristaltic pump. The angiogenic potential and inflammatory properties of hDPSCs were evaluated through reverse phase protein microarrays (RPPA), confocal immunofluorescence and western blot analyses.

resultsOur data showed that hDPSCs expressed the typical endothelial markers, which were up-regulated after endothelial induction, and were able to form tube-like structures. RPPA analyses revealed that these properties were modulated when a pulsatile unidirectional flow shear stress was applied to hDPSCs. Stem cells also revealed a downregulation of the immune-modulatory molecule PD-L1, in parallel with an up-regulation of the pro-inflammatory molecule NF-kB. Immune-modulatory properties of hDPSCs were also reduced after culture under flow-dependent shear stress and exposure to an inflammatory microenvironment. This evidence was strengthened by the detection of up-regulated levels of expression of pro-inflammatory cytokines in PBMCs.

conclusionsIn conclusion, the application of a pulsatile unidirectional flow shear stress induced a modulation of immunomodulatory/inflammatory properties of dental pulp pericyte-like cells.

Indexed as

Endothelial CellsPericytesDental PulpHumansLeukocytes, MononuclearStem CellsAngiogenesisDental pulp stem cellsFlow-dependent shear stressInflammationNeural crestPericytes

Identifiers

PMID36805780
PMCPMC9938980
OpenAlexW4321331013

What OpenQuestion holds

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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.