Carbon Nanotube-Hydrogel Composites Facilitate Neuronal Differentiation While Maintaining Homeostasis of Network Activity
Overview
Authors
Affiliations
It is often assumed that carbon nanotubes (CNTs) stimulate neuronal differentiation by transferring electrical signals and enhancing neuronal excitability. Given this, CNT-hydrogel composites are regarded as potential materials able to combine high electrical conductivity with biocompatibility, and therefore promote nerve regeneration. However, whether CNT-hydrogel composites actually influence neuronal differentiation and maturation, and how they do so remain elusive. In this study, CNT-hydrogel composites are prepared by in situ polymerization of poly(ethylene glycol) around a preformed CNT meshwork. It is demonstrated that the composites facilitate long-term survival and differentiation of pheochromocytoma 12 cells. Adult neural stem cells cultured on the composites show an increased neuron-to-astrocyte ratio and higher synaptic connectivity. Moreover, primary hippocampal neurons cultured on composites maintain morphological synaptic features as well as their neuronal network activity evaluated by spontaneous calcium oscillations, which are comparable to neurons cultured under control conditions. These results indicate that the composites are promising materials that could indeed facilitate neuronal differentiation while maintaining neuronal homeostasis.
Zhang J, Yang X, Wang S, Dong J, Zhang M, Zhang M Mater Today Bio. 2025; 29():101347.
PMID: 39850274 PMC: 11754139. DOI: 10.1016/j.mtbio.2024.101347.
Redolfi Riva E, Ozkan M, Stellacci F, Micera S Front Cell Dev Biol. 2024; 12:1491260.
PMID: 39568507 PMC: 11576468. DOI: 10.3389/fcell.2024.1491260.
Advanced Hydrogels: Enhancing Tissue Bioengineering with RGD Peptides and Carbon Nanomaterials.
M Galindo J, Merino S, Herrero M ChemMedChem. 2024; 20(3):e202400587.
PMID: 39446356 PMC: 11793852. DOI: 10.1002/cmdc.202400587.
Co-culture models for investigating cellular crosstalk in the glioma microenvironment.
Niu X, Zhang Y, Wang Y Cancer Pathog Ther. 2024; 2(4):219-230.
PMID: 39371093 PMC: 11447344. DOI: 10.1016/j.cpt.2023.11.002.
Yang X, Zhao Y, Liu W, Gao Z, Wang C, Wang C Biophys Rep. 2024; 10(4):241-253.
PMID: 39281200 PMC: 11399890. DOI: 10.52601/bpr.2024.240011.