Silk-Based Matrices and c-Kit-Positive Cardiac Progenitor Cells for a Cellularized Silk Fibroin Scaffold: Study of an in vivo Model.


Journal

Cells, tissues, organs
ISSN: 1422-6421
Titre abrégé: Cells Tissues Organs
Pays: Switzerland
ID NLM: 100883360

Informations de publication

Date de publication:
2023
Historique:
received: 22 07 2021
accepted: 10 02 2022
medline: 5 6 2023
pubmed: 15 2 2022
entrez: 14 2 2022
Statut: ppublish

Résumé

The production of a cellularized silk fibroin scaffold is very difficult because it is actually impossible to differentiate cells into a well-organized cardiac tissue. Without vascularization, not only do cell masses fail to grow, but they may also exhibit an area of necrosis, indicating a lack of oxygen and nutrients. In the present study, we used the so-called tyrosine protein kinase kit (c-Kit)-positive cardiac progenitor cells (CPCs) to generate cardiac cellularized silk fibroin scaffolds, multipotent cells isolated from the adult heart to date that can show some degree of differentiation toward the cardiac phenotype. To test their ability to differentiate into the cardiac phenotype in vivo as well, CPC and collagen organoid-like masses were implanted into nude mice and their behavior observed. Since the 3-dimensional structure of cardiac tissue can be preserved by scaffolds, we prepared in parallel different silk fibroin scaffolds with 3 different geometries and tested their behavior in 3 different models of immunosuppressed animals. Unfortunately, CPC cellularized silk fibroin scaffolds cannot be used in vivo. CPCs implanted alone or in collagen type I gel were destroyed by CD3+ lymphocyte aggregates, whereas the porous and partially oriented scaffolds elicited a consistent foreign body response characterized by giant cells. Only the electrospun meshes were resistant to the foreign body reaction. In conclusion, c-Kit-positive CPCs, although expressing a good level of cardiac differentiation markers in vitro with or without fibroin meshes, are not suitable for an in vivo model of cardiac organoids because they are degraded by a T-cell-mediated immune response. Even scaffolds which may preserve the survival of these cells in vivo also induced a host response. However, among the tested scaffolds, the electrospun meshes (F-scaffold) induced a lower response compared to all the other tested structures.

Identifiants

pubmed: 35158354
pii: 000522568
doi: 10.1159/000522568
doi:

Substances chimiques

Fibroins 9007-76-5
Silk 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

258-271

Informations de copyright

© 2022 S. Karger AG, Basel.

Auteurs

Antonella Motta (A)

Department of Industrial Engineering and Biotech Research Center, University of Trento, Trento, Italy.
European Institute of Excellence in Tissue Engineering and Regenerative Medicine, Trento, Italy.
INSTM Research Unit, Trento, Italy.

Rosario Barone (R)

Department of Biomedicine, Neurosciences and Advanced Diagnostics, University of Palermo, Palermo, Italy.

Filippo Macaluso (F)

SMART Engineering Solutions and Technologies (SMARTEST) Research Center, eCampus University, Palermo, Italy.

Filippo Giambalvo (F)

Department of Biomedicine, Neurosciences and Advanced Diagnostics, University of Palermo, Palermo, Italy.

Francesco Pecoraro (F)

Department of Biomedicine, Neurosciences and Advanced Diagnostics, University of Palermo, Palermo, Italy.

Patrizia Di Marco (P)

Istituto Zooprofilattico Sperimentale della Sicilia, Palermo, Italy.

Giovanni Cassata (G)

Istituto Zooprofilattico Sperimentale della Sicilia, Palermo, Italy.

Roberto Puleio (R)

Istituto Zooprofilattico Sperimentale della Sicilia, Palermo, Italy.

Claudio Migliaresi (C)

Department of Industrial Engineering and Biotech Research Center, University of Trento, Trento, Italy.
European Institute of Excellence in Tissue Engineering and Regenerative Medicine, Trento, Italy.
INSTM Research Unit, Trento, Italy.

Annalisa Guercio (A)

Istituto Zooprofilattico Sperimentale della Sicilia, Palermo, Italy.

Valentina Di Felice (V)

Department of Biomedicine, Neurosciences and Advanced Diagnostics, University of Palermo, Palermo, Italy.

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Classifications MeSH