Pleiotrophin: Analysis of the endothelialisation potential.


Journal

Advances in medical sciences
ISSN: 1898-4002
Titre abrégé: Adv Med Sci
Pays: Netherlands
ID NLM: 101276222

Informations de publication

Date de publication:
Mar 2019
Historique:
received: 19 12 2017
revised: 29 06 2018
accepted: 31 08 2018
pubmed: 21 1 2019
medline: 21 11 2019
entrez: 21 1 2019
Statut: ppublish

Résumé

Endothelialisation of vascular substitutes, in fact, remains one of the most unsolved problems in cardiovascular diseases treatment. Stromal Derived Factor 1 (SDF-1) has been largely investigated as an endothelialisation promoter and Pleiotrophin is a promising alternative. Although it has been known to exert beneficial effects on different cell types, its potential as an inducer of proliferation and migration of endothelial cells was not investigated. Therefore, this work is aimed to compare the effects of Pleiotrophin on proliferation and migration of endothelial cells with respect to SDF-1. Endothelial cell line EA.hy926 was treated with Pleiotrophin (50 ng/ml) or SDF-1 (50 ng/ml). Cell viability was evaluated by MTT assay and migration assays were performed in Transwell chambers. Wound healing potential was evaluated by scratch wound assay. CXCR4, RPTP β/ζ, PCNA and Rac1 expression was detected by Western Blot. Interestingly, Pleiotrophin significantly increased the viability of the treated endothelial cells with respects to SDF-1. The migratory ability of the endothelial cells was also improved in the presence of Pleiotrophin with reference to the SDF-1 treatment. Moreover, Western Blot analysis showed how the treatment with Pleiotrophin can induce an increase in the expression of RPTP β/ζ, PCNA and Rac1 compared to SDF-1. Due to the significant effects exerted on viability, migration and repair ability of endothelial cells compared to SDF-1, Pleiotrophin can be considered as an interesting molecule to promote re-endothelialisation.

Identifiants

pubmed: 30660899
pii: S1896-1126(18)30335-3
doi: 10.1016/j.advms.2018.08.007
pii:
doi:

Substances chimiques

Carrier Proteins 0
Cytokines 0
Proliferating Cell Nuclear Antigen 0
pleiotrophin 134034-50-7
rac1 GTP-Binding Protein EC 3.6.5.2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

144-151

Informations de copyright

Copyright © 2019 Medical University of Bialystok. Published by Elsevier B.V. All rights reserved.

Auteurs

Francesco Copes (F)

Laboratory of Human Anatomy, Department of Health Sciences, University of Piemonte Orientale, Novara, Italy; Laboratory for Biomaterials and Bioengineering, Canada Research Chair Tier I in Biomaterials and Bioengineering for the Innovation in Surgery, Department of Min-Met-Materials Engineering & CHU de Quebec Research Center, Laval University, Quebec City, Quebec, Canada.

Martina Ramella (M)

Laboratory of Human Anatomy, Department of Health Sciences, University of Piemonte Orientale, Novara, Italy.

Luca Fusaro (L)

Laboratory of Human Anatomy, Department of Health Sciences, University of Piemonte Orientale, Novara, Italy; Tissuegraft srl, Novara, Italy.

Diego Mantovani (D)

Laboratory for Biomaterials and Bioengineering, Canada Research Chair Tier I in Biomaterials and Bioengineering for the Innovation in Surgery, Department of Min-Met-Materials Engineering & CHU de Quebec Research Center, Laval University, Quebec City, Quebec, Canada.

Mario Cannas (M)

Laboratory of Human Anatomy, Department of Health Sciences, University of Piemonte Orientale, Novara, Italy.

Francesca Boccafoschi (F)

Laboratory of Human Anatomy, Department of Health Sciences, University of Piemonte Orientale, Novara, Italy. Electronic address: francesca.boccafoschi@med.uniupo.it.

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Classifications MeSH