Improved human islets' viability and functionality with mesenchymal stem cells and arg-gly-asp tripeptides supplementation of alginate micro-encapsulated islets in vitro.


Journal

Biochemical and biophysical research communications
ISSN: 1090-2104
Titre abrégé: Biochem Biophys Res Commun
Pays: United States
ID NLM: 0372516

Informations de publication

Date de publication:
06 08 2020
Historique:
received: 20 04 2020
accepted: 15 05 2020
pubmed: 10 6 2020
medline: 5 2 2021
entrez: 10 6 2020
Statut: ppublish

Résumé

The extension of islet transplantation to a wider number of type 1 diabetes patients is compromised by severe adverse events related to the immunosuppressant therapy required for allogenic islet transplantation. In this context, microencapsulation offers the prospects of immunosuppressive-free therapy by physically isolating islets from the immune system. However, current biomaterials need to be optimized to: improve biocompatibility, guaranty the maintenance of graft viability and functionality, and prevent fibrosis overgrowth around the capsule in vivo. Accumulating evidence suggest that mesenchymal stem cells (MSCs) and anchor points consisting of tripeptides arg-gly-asp (RGD) have cytoprotective effects on pancreatic islets. Here, we investigated the effect of supplementing reference M-rich alginate microcapsules with MSCs and RGD-G rich alginate on bioprocessing as well as on human pancreatic islets viability and functionality. We characterized the microcapsules components, and then for the new microcapsule composite product: we analyzed the empty capsules biocompatibility and then investigated the benefits of MSCs and RGD-G rich alginate on viability and functionality on the encapsulated human pancreatic islets in vitro. We performed viability tests by confocal microscopy and glucose stimulated insulin secretion (GSIS) test in vitro to assess the functionality of naked and encapsulated islets. Encapsulation in reference M-rich alginate capsules induced a reduction in viability and functionality compared to naked islets. This side-effect of encapsulation was in part counteracted by the presence of MSCs but the restoration was complete with the combination of both MSCs and the RGD-G rich alginate. The present findings show that bioprocessing a favorable composite environment inside the M-rich alginate capsule with both MSCs and RGD-G rich alginate improves human islets survival and functionality in vitro.

Identifiants

pubmed: 32513541
pii: S0006-291X(20)31027-5
doi: 10.1016/j.bbrc.2020.05.107
pii:
doi:

Substances chimiques

Alginates 0
Oligopeptides 0
arginyl-glycyl-aspartic acid 78VO7F77PN

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

650-657

Subventions

Organisme : NIDDK NIH HHS
ID : U24 DK098085
Pays : United States

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Camille Laporte (C)

Laboratory of Fundamental and Applied Bioenergetics (LBFA), INSERM U1055 and SFR Environmental and Systems Biology (BEeSy), University Grenoble Alps, Grenoble, France.

Emily Tubbs (E)

Laboratory of Fundamental and Applied Bioenergetics (LBFA), INSERM U1055 and SFR Environmental and Systems Biology (BEeSy), University Grenoble Alps, Grenoble, France. Electronic address: tubbsemily@gmail.com.

Maxime Pierron (M)

Univ. Grenoble Alpes, CEA, LETI, Technologies for Healthcare and Biology Division, Microfluidic Systems and Bioengineering Lab, F-38000, Grenoble, France.

Amanda Gallego (A)

Nanoimmunotech S.L, Vigo, Pontevedra, Spain.

Anaïck Moisan (A)

Cell Therapy and Engineering Unit, EFS, Auvergne Rhône Alps, Saint Ismier, France.

Frédéric Lamarche (F)

Laboratory of Fundamental and Applied Bioenergetics (LBFA), INSERM U1055 and SFR Environmental and Systems Biology (BEeSy), University Grenoble Alps, Grenoble, France.

Tamara Lozano (T)

Nanoimmunotech S.L, Vigo, Pontevedra, Spain.

Andrea Hernandez (A)

Nanoimmunotech S.L, Vigo, Pontevedra, Spain.

Cécile Cottet-Rousselle (C)

Laboratory of Fundamental and Applied Bioenergetics (LBFA), INSERM U1055 and SFR Environmental and Systems Biology (BEeSy), University Grenoble Alps, Grenoble, France.

Anne-Sophie Gauchez (AS)

Biology Institute, Grenoble Alps University Hospital, Grenoble, France.

Virginie Persoons (V)

Cell Therapy and Engineering Unit, EFS, Auvergne Rhône Alps, Saint Ismier, France.

Frédéric Bottausci (F)

Univ. Grenoble Alpes, CEA, LETI, Technologies for Healthcare and Biology Division, Microfluidic Systems and Bioengineering Lab, F-38000, Grenoble, France.

Caroline Fontelaye (C)

Univ. Grenoble Alpes, CEA, LETI, Technologies for Healthcare and Biology Division, Microfluidic Systems and Bioengineering Lab, F-38000, Grenoble, France.

François Boizot (F)

Univ. Grenoble Alpes, CEA, LETI, Technologies for Healthcare and Biology Division, Microfluidic Systems and Bioengineering Lab, F-38000, Grenoble, France.

Sandrine Lablanche (S)

Laboratory of Fundamental and Applied Bioenergetics (LBFA), INSERM U1055 and SFR Environmental and Systems Biology (BEeSy), University Grenoble Alps, Grenoble, France; Grenoble University Hospital, Grenoble, France.

Florence Rivera (F)

Univ. Grenoble Alpes, CEA, LETI, Technologies for Healthcare and Biology Division, Microfluidic Systems and Bioengineering Lab, F-38000, Grenoble, France.

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Classifications MeSH