Research ArticleSpecial Topic: Two-Dimensional Biomaterials in Regenerative Medicine
Sculpting neurotransmission during synaptic development by 2D nanostructured interfaces

https://doi.org/10.1016/j.nano.2017.01.020Get rights and content
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Abstract

Carbon nanotube-based biomaterials critically contribute to the design of many prosthetic devices, with a particular impact in the development of bioelectronics components for novel neural interfaces. These nanomaterials combine excellent physical and chemical properties with peculiar nanostructured topography, thought to be crucial to their integration with neural tissue as long-term implants. The junction between carbon nanotubes and neural tissue can be particularly worthy of scientific attention and has been reported to significantly impact synapse construction in cultured neuronal networks. In this framework, the interaction of 2D carbon nanotube platforms with biological membranes is of paramount importance. Here we study carbon nanotube ability to interfere with lipid membrane structure and dynamics in cultured hippocampal neurons. While excluding that carbon nanotubes alter the homeostasis of neuronal membrane lipids, in particular cholesterol, we document in aged cultures an unprecedented functional integration between carbon nanotubes and the physiological maturation of the synaptic circuits.

Graphical Abstract

MWCNTs alter the stability of membrane lipids, in particular cholesterol, in artificial lipid membranes. Conversely, they do not interfere with lipid membrane structure, such as lipid rafts, or dynamics in cultured hippocampal neurons.

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Abbreviations

AFM
atomic force microscopy
CT-B
Cholera Toxin subunit-B
DIV
days in vitro
DOPC
1,2-Dioleoyl-sn-glycero-3-phosphocholine
MβCD
Methyl-β-Cyclodextrin
mPSCs
miniature post-synaptic currents
MWCNTs
multi-walled carbon nanotubes
PSCs
post-synaptic currents
SLM
artificial lipid membranes
SPM
scanning probe microscopy
TTX
Tetrodotoxin
VGLUT1
vesicular glutamate transporter 1

Key words

Nanostructured materials
Patch clamp
Cholesterol
Synaptic release
Vesicle pools

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Financial supports from: This work was supported by the ByAxon n. 737116, NEUROSCAFFOLDS-FP7-NMP-604263 and the PRIN-MIUR n. 2012MYESZW to L.B.

Competing interests: The Authors declare no competing financial interests.

Authors' contributions: NPP performed electrophysiology, immunocytochemistry and confocal microscopy experiments and contributed to the analysis. DS and FP performed SLM experiments and AFM analysis. SB and MP provided the materials. LB and DS conceived the idea and designed the experiments. LB and DS wrote the manuscript. LB provided funding. All authors read and approved the final manuscript.