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Advanced real-time recordings of neuronal activity with tailored patch pipettes, diamond multi-electrode arrays and electrochromic voltage-sensitive dyes

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出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00424-020-02472-4

关键词

Patch clamp; Fast cellular perfusion; Multi-electrode recording; Diamond sensors; Voltage-sensitive dyes; Two-photon microscopy

资金

  1. Project FAR (Fondo di Ateneo per la Ricerca) 2016-2019 of the University of Ferrara
  2. Project FIR (Fondi per l'Incentivazione della Ricerca) 2016 of the University of Ferrara
  3. OIST Graduate University, Okinawa, Japan
  4. Italian Miur [2015FNWP34]
  5. Compagnia di San Paolo [CSTO165284]

向作者/读者索取更多资源

To understand the workings of the nervous system, it is essential to develop advanced techniques for real-time recording of neuronal electrical activity and to study how higher functions emerge from coordinated activity. Techniques such as patch pipettes and biocompatible probes allow for recording from single neurons and multiple neurons simultaneously, providing valuable insights into neuronal activity and function. Advanced methods like voltage imaging with fast voltage-sensitive dyes and two-photon microscopy offer high spatial resolution for studying voltage oscillations in the brain and dendritic voltage changes in awake animals.
To understand the working principles of the nervous system is key to figure out its electrical activity and how this activity spreads along the neuronal network. It is therefore crucial to develop advanced techniques aimed to record in real time the electrical activity, from compartments of single neurons to populations of neurons, to understand how higher functions emerge from coordinated activity. To record from single neurons, a technique will be presented to fabricate patch pipettes able to seal on any membrane with a single glass type and whose shanks can be widened as desired. This dramatically reduces access resistance during whole-cell recording allowing fast intracellular and, if required, extracellular perfusion. To simultaneously record from many neurons, biocompatible probes will be described employing multi-electrodes made with novel technologies, based on diamond substrates. These probes also allow to synchronously record exocytosis and neuronal excitability and to stimulate neurons. Finally, to achieve even higher spatial resolution, it will be shown how voltage imaging, employing fast voltage-sensitive dyes and two-photon microscopy, is able to sample voltage oscillations in the brain spatially resolved and voltage changes in dendrites of single neurons at millisecond and micrometre resolution in awake animals.

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