Stimulation and imaging of neural cells via photonic nanojets

Abstract

Various neuromodulation techniques have been developed to modulate the peak activity of neurons, thereby regulating brain function and alleviating neurological disorders. Additionally, neuronal stimulation and imaging have significantly contributed to the understanding and treatment of these diseases. Here, we propose utilizing photonic nanojets for optical stimulation and imaging of neural cells. The application of resin microspheres as microlenses enhances fluorescence imaging of neural lysosomes, mitochondria, and actin filaments by generating photonic nanojets. Moreover, optical tweezers can precisely manipulate the microlenses to locate specific targets within the cell for real-time stimulation and imaging. The focusing capabilities of these microlenses enable subcellular-level spatial precision in stimulation, allowing highly accurate targeting of neural cells while minimizing off-target effects. Furthermore, fluorescent signals during neural cell stimulation can be detected in real-time using these microlenses. The proposed method facilitates investigation into intercellular signal transmission among neural cells, providing new insights into the underlying mechanisms of neuronal cell activities at a subcellular level.