Advanced NeuronalModulation with Semiconducting GraphiticCarbon Nitride: Insights from <i>In Vitro</i>, <i>InVivo</i>, and <i>In Silico</i> Studies

Impaired neuronal functions and cell death within ailments such as neurodegenerative Parkinson’s disease pose significant challenges due to their complex pathophysiology and limited treatment options. In this landscape, innovative materials with unique physicochemical properties that ameliorate the debilitated neuronal functions are critically required. Neuronal functions rely on the conduction of nerve impulses, a process that can be effectively targeted using advanced materials that exhibit conducive properties essential for modulating neural activity. For their semiconductor characteristics, combined with well-suited biocompatibility, graphitic carbon nitride (g-C<sub>3</sub>N<sub>4</sub>) nanosheets provide promising avenues for such neurotherapeutic applications. Our multidisciplinary study investigates the potential of g-C<sub>3</sub>N<sub>4</sub> nanosheets in promoting neuronal differentiation and network formation across <i>in vitro</i> and <i>in vivo</i> systems. SH-SY5Y cells exposed to g-C<sub>3</sub>N<sub>4</sub> demonstrated enhanced neuronal differentiation and neuritic outgrowth over a chronic 21-days period, accompanied by an increased intracellular Ca<sup>2+</sup> influx, pivotal for dopamine biosynthesis, as evidenced by the upregulated expression of vesicular monoamine transporter 2 (VMAT2), aromatic l-amino acid decarboxylase (AADC), and tyrosine hydroxylase (TH) genes. Utilizing transgenic Caenorhabditis elegans model expressing human α-synuclein, we observed the neuroprotective potential of g-C<sub>3</sub>N<sub>4</sub>, as evidenced by reduced protein aggregation and improved dopaminergic functions. In the pursuit of exploring the mechanism of g-C<sub>3</sub>N<sub>4</sub>-induced neuronal stimulation, the semiconducting nature of g-C<sub>3</sub>N<sub>4</sub> came forth, which was further validated using theoretical (<i>in silico</i>) models. These models demonstrated an increase in the chemical potential of the material upon the application of electrical biases. Studying Ca<sup>2+</sup> channel inhibition, we also observed that phenotypic and molecular effects were the outcomes of the stimulation caused due to the presence of g-C<sub>3</sub>N<sub>4</sub> nanosheets. Our findings, supported by experimental and <i>in silico</i> studies, suggest that g-C<sub>3</sub>N<sub>4</sub> nanosheets can effectively modulate neuronal behavior through their semiconducting properties, offering promising avenues for therapeutic interventions in neurodegenerative diseases.

Publication Details

Journal
Figshare
Published
2025-02-04
DOI
https://doi.org/10.1021/acsami.4c19242.s001
Primary Topic
Graphene and Nanomaterials Applications
Type
article
Field-Weighted Citation Impact
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article

Advanced NeuronalModulation with Semiconducting GraphiticCarbon Nitride: Insights from In Vitro, InVivo, and In Silico Studies

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Graphene and Nanomaterials Applications
article

Advanced NeuronalModulation with Semiconducting GraphiticCarbon Nitride: Insights from In Vitro, InVivo, and In Silico Studies

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Abstract

Impaired neuronal functions and cell death within ailments such as neurodegenerative Parkinson’s disease pose significant challenges due to their complex pathophysiology and limited treatment options. In this landscape, innovative materials with unique physicochemical properties that ameliorate the debilitated neuronal functions are critically required. Neuronal functions rely on the conduction of nerve impulses, a process that can be effectively targeted using advanced materials that exhibit conducive properties essential for modulating neural activity. For their semiconductor characteristics, combined with well-suited biocompatibility, graphitic carbon nitride (g-C<sub>3</sub>N<sub>4</sub>) nanosheets provide promising avenues for such neurotherapeutic applications. Our multidisciplinary study investigates the potential of g-C<sub>3</sub>N<sub>4</sub> nanosheets in promoting neuronal differentiation and network formation across <i>in vitro</i> and <i>in vivo</i> systems. SH-SY5Y cells exposed to g-C<sub>3</sub>N<sub>4</sub> demonstrated enhanced neuronal differentiation and neuritic outgrowth over a chronic 21-days period, accompanied by an increased intracellular Ca<sup>2+</sup> influx, pivotal for dopamine biosynthesis, as evidenced by the upregulated expression of vesicular monoamine transporter 2 (VMAT2), aromatic l-amino acid decarboxylase (AADC), and tyrosine hydroxylase (TH) genes. Utilizing transgenic Caenorhabditis elegans model expressing human α-synuclein, we observed the neuroprotective potential of g-C<sub>3</sub>N<sub>4</sub>, as evidenced by reduced protein aggregation and improved dopaminergic functions. In the pursuit of exploring the mechanism of g-C<sub>3</sub>N<sub>4</sub>-induced neuronal stimulation, the semiconducting nature of g-C<sub>3</sub>N<sub>4</sub> came forth, which was further validated using theoretical (<i>in silico</i>) models. These models demonstrated an increase in the chemical potential of the material upon the application of electrical biases. Studying Ca<sup>2+</sup> channel inhibition, we also observed that phenotypic and molecular effects were the outcomes of the stimulation caused due to the presence of g-C<sub>3</sub>N<sub>4</sub> nanosheets. Our findings, supported by experimental and <i>in silico</i> studies, suggest that g-C<sub>3</sub>N<sub>4</sub> nanosheets can effectively modulate neuronal behavior through their semiconducting properties, offering promising avenues for therapeutic interventions in neurodegenerative diseases.

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