Cytoskeleton adaptation to stretchable surface relaxation improves adherent cryopreservation of human mesenchymal stem cells.

Cryopreservation adherent cell monolayer compression cytoskeleton human umbilical cord mesenchymal stem cells silicone stretching apparatus

Journal

Cryobiology
ISSN: 1090-2392
Titre abrégé: Cryobiology
Pays: Netherlands
ID NLM: 0006252

Informations de publication

Date de publication:
05 Sep 2024
Historique:
received: 04 06 2024
revised: 29 07 2024
accepted: 22 08 2024
medline: 8 9 2024
pubmed: 8 9 2024
entrez: 7 9 2024
Statut: aheadofprint

Résumé

Adherent cell systems are usually dissociated before being cryopreserved, as standard protocols are established for cells in suspension. The application of standard procedures to more complex systems, sensitive to dissociation, such as adherent monolayers, especially comprising mature cell types, or tissues, remains unsatisfactory. Uncontrolled cell detachment due to intracellular tensile stress, membrane ruptures and damages of adhesion proteins are common during freezing and thawing of cell monolayers. However, many therapeutically relevant cell systems grow adherently to develop their native morphology and functionality, but lose their integrity after dissociation. The hypothesis is that cells on stretchable substrates have a more adaptable cytoskeleton and membrane, reducing cryopreservation-induced stress. Our studies investigate the influence of stretchable surfaces on the cryopreservation of adherent cells to avoid harmful dissociation and expedite post-thawing cultivation of functional cells. A stretching apparatus for defined radial stretching, consisting of silicone vessels and films with specific surface textures for cell culture, were developed. Adherent human umbilical cord mesenchymal stem cells (hUC-MSCs) were cultivated on a stretched silicone film within the vessel, forming a monolayer that were compressed by relaxation, while remaining attached to the relaxed film. Compressed hUC-MSCs, which were cryopreserved adherently showed higher viability and less detachment after thawing compared to control cells without compression. Within three to seven days post-thawing, the hUC-MSCs recovered, and the monolayer reformed. These experiments support the hypothesis that cryopreservation success of adherent cell systems is enhanced by improved adaptability of the cytoskeleton and cell membrane, opening up new approaches in cryobiotechnology.

Identifiants

pubmed: 39243925
pii: S0011-2240(24)00113-5
doi: 10.1016/j.cryobiol.2024.104958
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104958

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors have no conflicts of interest to declare.

Auteurs

Saskia Altmaier (S)

Department of Molecular and Cellular Biotechnology, Saarland University, 66123 Saarbrücken, Germany; Department of Cryosensor Technology, Fraunhofer Institute for Biomedical Engineering (IBMT), Joseph-von-Fraunhofer-Weg 1, 66820 Sulzbach, Germany.

Ronan Le Harzic (R)

Department of Cryosensor Technology, Fraunhofer Institute for Biomedical Engineering (IBMT), Joseph-von-Fraunhofer-Weg 1, 66820 Sulzbach, Germany.

Frank Stracke (F)

Department of Cryosensor Technology, Fraunhofer Institute for Biomedical Engineering (IBMT), Joseph-von-Fraunhofer-Weg 1, 66820 Sulzbach, Germany.

Anna Martina Speicher (AM)

Department of Cryosensor Technology, Fraunhofer Institute for Biomedical Engineering (IBMT), Joseph-von-Fraunhofer-Weg 1, 66820 Sulzbach, Germany.

Detlev Uhl (D)

Center Smart Materials and Adaptive Systems (CeSMA), Fraunhofer Institute for Silicate Research ISC, Neunerplatz 2, 97082 Würzburg, Germany.

Johannes Ehrlich (J)

Center Smart Materials and Adaptive Systems (CeSMA), Fraunhofer Institute for Silicate Research ISC, Neunerplatz 2, 97082 Würzburg, Germany.

Thomas Gerlach (T)

Center Smart Materials and Adaptive Systems (CeSMA), Fraunhofer Institute for Silicate Research ISC, Neunerplatz 2, 97082 Würzburg, Germany.

Katharina Schmidt (K)

Department of Cryosensor Technology, Fraunhofer Institute for Biomedical Engineering (IBMT), Joseph-von-Fraunhofer-Weg 1, 66820 Sulzbach, Germany.

Katja Lemmer (K)

Department of Cryosensor Technology, Fraunhofer Institute for Biomedical Engineering (IBMT), Joseph-von-Fraunhofer-Weg 1, 66820 Sulzbach, Germany.

Franziska Lautenschläger (F)

Division of Cytoskeleton Fibers, Saarland University, 66123 Saarbrücken, Germany.

Holger Böse (H)

Center Smart Materials and Adaptive Systems (CeSMA), Fraunhofer Institute for Silicate Research ISC, Neunerplatz 2, 97082 Würzburg, Germany.

Julia C Neubauer (JC)

Department of Cryosensor Technology, Fraunhofer Institute for Biomedical Engineering (IBMT), Joseph-von-Fraunhofer-Weg 1, 66820 Sulzbach, Germany.

Heiko Zimmermann (H)

Department of Molecular and Cellular Biotechnology, Saarland University, 66123 Saarbrücken, Germany; Department of Cryosensor Technology, Fraunhofer Institute for Biomedical Engineering (IBMT), Joseph-von-Fraunhofer-Weg 1, 66820 Sulzbach, Germany; Facultad de Ciencias del Mar, Universidad Católica del Norte, 1780000 Coquimbo, Chile.

Ina Meiser (I)

Department of Cryosensor Technology, Fraunhofer Institute for Biomedical Engineering (IBMT), Joseph-von-Fraunhofer-Weg 1, 66820 Sulzbach, Germany. Electronic address: ina.meiser@ibmt.fraunhofer.de.

Classifications MeSH