An investigation of functionalized chitosan and alginate multilayer conformal nanocoating on mouse beta cell spheroids as a model for pancreatic islet transplantation.

Conformal coating Diabetes Islet transplantation Layer-by-layer Nano encapsulation T1D

Journal

International journal of biological macromolecules
ISSN: 1879-0003
Titre abrégé: Int J Biol Macromol
Pays: Netherlands
ID NLM: 7909578

Informations de publication

Date de publication:
21 Aug 2024
Historique:
received: 15 05 2024
revised: 09 08 2024
accepted: 20 08 2024
medline: 24 8 2024
pubmed: 24 8 2024
entrez: 23 8 2024
Statut: aheadofprint

Résumé

Multilayer conformal coatings have been shown to provide a nanoscale barrier between cells and their environment with adequate stability, while regulating the diffusion of nutrition and waste across the cell membrane. The coating method aims to minimize capsule thickness and implant volume while reducing the need for immunosuppressive drugs, making it a promising approach for islet cell encapsulation in clinical islet transplantation for the treatment of Type 1 diabetes. This study introduces an immunoprotective nanocoating obtained through electrostatic interaction between quaternized phosphocholine-chitosan (PC-QCH) and tetrahydropyran triazole phenyl-alginate (TZ-AL) onto mouse β-cell spheroids. First, successful synthesis of the proposed polyelectrolytes was confirmed with physico-chemical characterization. A coating with an average thickness of 540 nm was obtained with self-assembly of 4-bilayers of PC-QCH/TZ-AL onto MIN6 β-cell spheroids. Surface coating of spheroids did not affect cell viability, metabolic activity, or insulin secretion, when compared to non-coated spheroids. The exposure of the polyelectrolytes to THP-1 monocyte-derived macrophages lead to a reduced level of TNF-α secretion and exposure of coated spheroids to RAW264.7 macrophages showed a decreasing trend in the secretion of TNF-α and IL-6. In addition, coated spheroids were able to establish normoglycemia when implanted into diabetic NOD-SCID mice, demonstrating in vivo biocompatibility and cellular function. These results demonstrate the ability of the PC-QCH/TZ-AL conformal coating to mitigate pro-inflammatory response from macrophages, and thus can be a promising candidate towards nanoencapsulation for cell-based therapy, particularly in type 1 diabetes, where the insulin secreting β-cells are subjected to inflammation and immune cell attack.

Identifiants

pubmed: 39179080
pii: S0141-8130(24)05765-9
doi: 10.1016/j.ijbiomac.2024.134960
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

134960

Informations de copyright

Copyright © 2024. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare no competing financial interest.

Auteurs

Michael Y Yitayew (MY)

Department of Biomedical Engineering, McGill University, 3775 Rue University, Montreal, QC H3A 2B4, Canada.

Marco Gasparini (M)

Department of Surgery, McGill University Health Centre, 1001 Boulevard Décarie, Montreal, QC H4A 3J1, Canada; Transplantation Immunology Laboratory, Research Institute of the McGill University Health Centre, 1001 Boulevard Décarie, Montreal, QC H4A 3J1, Canada.

Ling Li (L)

Department of Biomedical Engineering, McGill University, 3775 Rue University, Montreal, QC H3A 2B4, Canada.

Steven Paraskevas (S)

Department of Surgery, McGill University Health Centre, 1001 Boulevard Décarie, Montreal, QC H4A 3J1, Canada; Transplantation Immunology Laboratory, Research Institute of the McGill University Health Centre, 1001 Boulevard Décarie, Montreal, QC H4A 3J1, Canada.

Maryam Tabrizian (M)

Department of Biomedical Engineering, McGill University, 3775 Rue University, Montreal, QC H3A 2B4, Canada; Faculty of Dental Medicine and Oral Health Sciences, McGill University, 2001 Avenue McGill College, Montreal, QC H3A 1G1, Canada. Electronic address: maryam.tabrizian@mcgill.ca.

Classifications MeSH