4.8 Article

Closed-Loop Real-Time Imaging Enables Fully Automated Cell-Targeted Patch-Clamp Neural Recording In Vivo

期刊

NEURON
卷 95, 期 5, 页码 1037-+

出版社

CELL PRESS
DOI: 10.1016/j.neuron.2017.08.011

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资金

  1. Jeremy and Joyce Wertheimer
  2. NIH [1R01NS102727, 1R01EY023173, 1R01MH103910]
  3. NIH Director's Pioneer Award [1DP1NS087724]
  4. MIT Synthetic Intelligence Project
  5. MIT Media Lab
  6. HHMI-Simons Faculty Scholars Program
  7. New York Stem Cell Foundation-Robertson Award

向作者/读者索取更多资源

Targeted patch-clamp recording is a powerful method for characterizing visually identified cells in intact neural circuits, but it requires skill to perform. We previously developed an algorithm that automates blind patching in vivo, but full automation of visually guided, targeted in vivo patching has not been demonstrated, with currently available approaches requiring human intervention to compensate for cell movement as a patch pipette approaches a targeted neuron. Here we present a closed-loop real-time imaging strategy that automatically compensates for cell movement by tracking cell position and adjusting pipette motion while approaching a target. We demonstrate our system's ability to adaptively patch, under continuous two-photon imaging and real-time analysis, fluorophore-expressing neurons of multiple types in the living mouse cortex, without human intervention, with yields comparable to skilled human experimenters. Our imagepatching robot is easy to implement and will help enable scalable characterization of identified cell types in intact neural circuits.

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