Impact of the physico-chemical properties of polymeric microspheres functionalized with cell adhesion molecules on the behavior of mesenchymal stromal cells.

Cell behavior Mesenchymal stromal cell Pharmacologically active microcarriers Physicochemical properties Polymer Regenerative medicine

Journal

Materials science & engineering. C, Materials for biological applications
ISSN: 1873-0191
Titre abrégé: Mater Sci Eng C Mater Biol Appl
Pays: Netherlands
ID NLM: 101484109

Informations de publication

Date de publication:
Feb 2021
Historique:
received: 01 11 2020
revised: 17 12 2020
accepted: 28 12 2020
entrez: 13 2 2021
pubmed: 14 2 2021
medline: 15 5 2021
Statut: ppublish

Résumé

Polymeric, biodegradable, microspheres (MS) presenting a biomimetic surface of extracellular matrix (ECM) proteins are currently used for transporting cells and/or encapsulated proteins for regenerative medicine studies. They can be made of (lactic-co-glycolic acid) (PLGA) or of a more hydrophilic PLGA-P188 (Poloxamer188)-PLGA polymer allowing for the complete release of the therapeutic proteins. They promote stem cell adhesion, cell survival and differentiation after transplantation. Although the biological effectiveness of these microcarriers is established, a detailed understanding of the protein and cell interactions with the microcarrier surface remain unclear due to a lack of information of their surface properties. The aim of this study was to characterize the physicochemical properties of two polymeric MS systems and determine the effect of laminin and poly-d-lysine coated microcarriers on stem cell adhesion, survival and neuronal differentiation. The hydrophobicity and topography of PLGA MS promoted protein adsorption and the stem cells quickly adhered and spread on the surface of these microcarriers. In contrast less proteins adsorbed onto PLGA-P188-PLGA MS and although cells adhered to these microcarriers, they remained round and did not spread on their surface. Despite these early-stage differences, our results suggest that the nature of the MS does not strongly influence the long-term cell behavior. The cells exhibit the same cell number, differentiation profile and ability to secrete ECM molecules regardless of the type of microcarrier used. Likely the ECM molecules that form a microenvironment around both of these 3D microcarrier/cell constructs over time play a role in this converging cell behavior. We have thus furthered our understanding of the physicochemical properties of polymeric cell carriers affecting stem cell behavior to help tailor suitable microcarriers for neuroregenerative applications.

Identifiants

pubmed: 33579486
pii: S0928-4931(20)33771-1
doi: 10.1016/j.msec.2020.111852
pii:
doi:

Substances chimiques

Cell Adhesion Molecules 0
Polylactic Acid-Polyglycolic Acid Copolymer 1SIA8062RS
Lactic Acid 33X04XA5AT

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

111852

Informations de copyright

Crown Copyright © 2021. Published by Elsevier B.V. All rights reserved.

Auteurs

Assia Rmaidi (A)

CRCINA-GLIAD, INSERM, Université de Nantes, Université d'Angers, 49933 Angers, France.

Mischa Zelzer (M)

School of Pharmacy, Biodiscovery Institute, University Park, University of Nottingham, Nottingham NG7 2RD, United Kingdom.

Laurence Sindji (L)

CRCINA-GLIAD, INSERM, Université de Nantes, Université d'Angers, 49933 Angers, France.

Raphaël Dima (R)

CRCINA-GLIAD, INSERM, Université de Nantes, Université d'Angers, 49933 Angers, France.

Frank Boury (F)

CRCINA-GLIAD, INSERM, Université de Nantes, Université d'Angers, 49933 Angers, France.

Nicolas Delorme (N)

Institut des Molécules et Matériaux du Mans (IMMM), Le Mans Université, UMR-CNRS 6283, 72085 Le Mans Cedex 9, France.

Claudia N Montero-Menei (CN)

CRCINA-GLIAD, INSERM, Université de Nantes, Université d'Angers, 49933 Angers, France. Electronic address: claudia.montero-menei@univ-angers.fr.

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Classifications MeSH