Rheological Characterization of Three-Dimensional Neuronal Cultures Embedded in PEGylated Fibrin Hydrogels

Three-dimensional (3D) neuronal cultures are valuable models for studying brain complexity in vitro, and the choice of the bulk material in which the neurons grow is a crucial factor in establishing successful cultures. Indeed, neuronal development and network functionality are influenced by the mec...

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Main Authors: Clara F. López-León, Jordi Soriano, Ramon Planet
Format: Article
Language:English
Published: MDPI AG 2023-08-01
Series:Gels
Subjects:
Online Access:https://www.mdpi.com/2310-2861/9/8/642
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author Clara F. López-León
Jordi Soriano
Ramon Planet
author_facet Clara F. López-León
Jordi Soriano
Ramon Planet
author_sort Clara F. López-León
collection DOAJ
description Three-dimensional (3D) neuronal cultures are valuable models for studying brain complexity in vitro, and the choice of the bulk material in which the neurons grow is a crucial factor in establishing successful cultures. Indeed, neuronal development and network functionality are influenced by the mechanical properties of the selected material; in turn, these properties may change due to neuron–matrix interactions that alter the microstructure of the material. To advance our understanding of the interplay between neurons and their environment, here we utilized a PEGylated fibrin hydrogel as a scaffold for mouse primary neuronal cultures and carried out a rheological characterization of the scaffold over a three-week period, both with and without cells. We observed that the hydrogels exhibited an elastic response that could be described in terms of the Young’s modulus <i>E</i>. The hydrogels without neurons procured a stable <inline-formula><math xmlns="http://www.w3.org/1998/Math/MathML" display="inline"><semantics><mrow><mi>E</mi><mo>≃</mo><mn>420</mn></mrow></semantics></math></inline-formula> Pa, while the neuron-laden hydrogels showed a higher <inline-formula><math xmlns="http://www.w3.org/1998/Math/MathML" display="inline"><semantics><mrow><mi>E</mi><mo>≃</mo><mn>590</mn></mrow></semantics></math></inline-formula> Pa during the early stages of development that decreased to <inline-formula><math xmlns="http://www.w3.org/1998/Math/MathML" display="inline"><semantics><mrow><mi>E</mi><mo>≃</mo><mn>340</mn></mrow></semantics></math></inline-formula> Pa at maturer stages. Our results suggest that neurons and their processes dynamically modify the hydrogel structure during development, potentially compromising both the stability of the material and the functional traits of the developing neuronal network.
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spelling doaj.art-08474894b4bd4786ab3722ea17d79a322023-11-19T01:13:41ZengMDPI AGGels2310-28612023-08-019864210.3390/gels9080642Rheological Characterization of Three-Dimensional Neuronal Cultures Embedded in PEGylated Fibrin HydrogelsClara F. López-León0Jordi Soriano1Ramon Planet2Departament de Física de la Matèria Condensada, Universitat de Barcelona, E-08028 Barcelona, SpainDepartament de Física de la Matèria Condensada, Universitat de Barcelona, E-08028 Barcelona, SpainDepartament de Física de la Matèria Condensada, Universitat de Barcelona, E-08028 Barcelona, SpainThree-dimensional (3D) neuronal cultures are valuable models for studying brain complexity in vitro, and the choice of the bulk material in which the neurons grow is a crucial factor in establishing successful cultures. Indeed, neuronal development and network functionality are influenced by the mechanical properties of the selected material; in turn, these properties may change due to neuron–matrix interactions that alter the microstructure of the material. To advance our understanding of the interplay between neurons and their environment, here we utilized a PEGylated fibrin hydrogel as a scaffold for mouse primary neuronal cultures and carried out a rheological characterization of the scaffold over a three-week period, both with and without cells. We observed that the hydrogels exhibited an elastic response that could be described in terms of the Young’s modulus <i>E</i>. The hydrogels without neurons procured a stable <inline-formula><math xmlns="http://www.w3.org/1998/Math/MathML" display="inline"><semantics><mrow><mi>E</mi><mo>≃</mo><mn>420</mn></mrow></semantics></math></inline-formula> Pa, while the neuron-laden hydrogels showed a higher <inline-formula><math xmlns="http://www.w3.org/1998/Math/MathML" display="inline"><semantics><mrow><mi>E</mi><mo>≃</mo><mn>590</mn></mrow></semantics></math></inline-formula> Pa during the early stages of development that decreased to <inline-formula><math xmlns="http://www.w3.org/1998/Math/MathML" display="inline"><semantics><mrow><mi>E</mi><mo>≃</mo><mn>340</mn></mrow></semantics></math></inline-formula> Pa at maturer stages. Our results suggest that neurons and their processes dynamically modify the hydrogel structure during development, potentially compromising both the stability of the material and the functional traits of the developing neuronal network.https://www.mdpi.com/2310-2861/9/8/642biomaterialsneuronal culturesrheological characterizationhydrogels
spellingShingle Clara F. López-León
Jordi Soriano
Ramon Planet
Rheological Characterization of Three-Dimensional Neuronal Cultures Embedded in PEGylated Fibrin Hydrogels
Gels
biomaterials
neuronal cultures
rheological characterization
hydrogels
title Rheological Characterization of Three-Dimensional Neuronal Cultures Embedded in PEGylated Fibrin Hydrogels
title_full Rheological Characterization of Three-Dimensional Neuronal Cultures Embedded in PEGylated Fibrin Hydrogels
title_fullStr Rheological Characterization of Three-Dimensional Neuronal Cultures Embedded in PEGylated Fibrin Hydrogels
title_full_unstemmed Rheological Characterization of Three-Dimensional Neuronal Cultures Embedded in PEGylated Fibrin Hydrogels
title_short Rheological Characterization of Three-Dimensional Neuronal Cultures Embedded in PEGylated Fibrin Hydrogels
title_sort rheological characterization of three dimensional neuronal cultures embedded in pegylated fibrin hydrogels
topic biomaterials
neuronal cultures
rheological characterization
hydrogels
url https://www.mdpi.com/2310-2861/9/8/642
work_keys_str_mv AT claraflopezleon rheologicalcharacterizationofthreedimensionalneuronalculturesembeddedinpegylatedfibrinhydrogels
AT jordisoriano rheologicalcharacterizationofthreedimensionalneuronalculturesembeddedinpegylatedfibrinhydrogels
AT ramonplanet rheologicalcharacterizationofthreedimensionalneuronalculturesembeddedinpegylatedfibrinhydrogels