Bioinspired microcone-array-based living biointerfaces: enhancing the anti-inflammatory effect and neuronal network formation.
Hongxu ChenLulu WangYi LuXuemin DuPublished in: Microsystems & nanoengineering (2020)
Implantable neural interfaces and systems have attracted much attention due to their broad applications in treating diverse neuropsychiatric disorders. However, obtaining a long-term reliable implant-neural interface is extremely important but remains an urgent challenge due to the resulting acute inflammatory responses. Here, bioinspired microcone-array-based (MA) interfaces have been successfully designed, and their cytocompatibility with neurons and the inflammatory response have been explored. Compared with smooth control samples, MA structures cultured with neuronal cells result in much denser extending neurites, which behave similar to creepers, wrapping tightly around the microcones to form complex and interconnected neuronal networks. After further implantation in mouse brains for 6 weeks, the MA probes (MAPs) significantly reduced glial encapsulation and neuron loss around the implants, suggesting better neuron viability at the implant-neural interfaces than that of smooth probes. This bioinspired strategy for both enhanced glial resistance and neuron network formation via a specific structural design could be a platform technology that not only opens up avenues for next-generation artificial neural networks and brain-machine interfaces but also provides universal approaches to biomedical therapeutics.
Keyphrases
- neural network
- inflammatory response
- small molecule
- cerebral ischemia
- soft tissue
- high throughput
- anti inflammatory
- high resolution
- induced apoptosis
- neuropathic pain
- liver failure
- fluorescence imaging
- single molecule
- cell cycle arrest
- endothelial cells
- white matter
- blood brain barrier
- deep learning
- lipopolysaccharide induced
- high density
- brain injury
- drug induced
- mass spectrometry
- acute respiratory distress syndrome
- single cell
- cell death
- hepatitis b virus
- extracorporeal membrane oxygenation