| Literature DB >> 30969898 |
Gregory L Holst1, William Stoy2, Bo Yang1, Ilya Kolb2, Suhasa B Kodandaramaiah3, Lu Li4, Ulf Knoblich4, Hongkui Zeng4, Bilal Haider2, Edward S Boyden5,6,7, Craig R Forest1.
Abstract
Patch clamping is the gold standard measurement technique for cell-type characterization in vivo, but it has low throughput, is difficult to scale, and requires highly skilled operation. We developed an autonomous robot that can acquire multiple consecutive patch-clamp recordings in vivo. In practice, 40 pipettes loaded into a carousel are sequentially filled and inserted into the brain, localized to a cell, used for patch clamping, and disposed. Automated visual stimulation and electrophysiology software enables functional cell-type classification of whole cell-patched cells, as we show for 37 cells in the anesthetized mouse in visual cortex (V1) layer 5. We achieved 9% yield, with 5.3 min per attempt over hundreds of trials. The highly variable and low-yield nature of in vivo patch-clamp recordings will benefit from such a standardized, automated, quantitative approach, allowing development of optimal algorithms and enabling scaling required for large-scale studies and integration with complementary techniques. NEW & NOTEWORTHY In vivo patch-clamp is the gold standard for intracellular recordings, but it is a very manual and highly skilled technique. The robot in this work demonstrates the most automated in vivo patch-clamp experiment to date, by enabling production of multiple, serial intracellular recordings without human intervention. The robot automates pipette filling, wire threading, pipette positioning, neuron hunting, break-in, delivering sensory stimulus, and recording quality control, enabling in vivo cell-type characterization.Entities:
Keywords: automated; in vivo; layer 5; patch clamp; robotic; visual cortex
Mesh:
Year: 2019 PMID: 30969898 PMCID: PMC6620702 DOI: 10.1152/jn.00738.2018
Source DB: PubMed Journal: J Neurophysiol ISSN: 0022-3077 Impact factor: 2.714