Change search
ReferencesLink to record
Permanent link

Direct link
Cortical Axons, Isolated in Channels, Display Activity-Dependent Signal Modulation as a Result of Targeted Stimulation
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Neuroscience, Clinical Neurophysiology. Swiss Fed Inst Technol, Dept Biosyst Sci & Engn, Bio Engn Lab, Basel, Switzerland..
Swiss Fed Inst Technol, Dept Biosyst Sci & Engn, Bio Engn Lab, Basel, Switzerland..
Swiss Fed Inst Technol, Dept Biosyst Sci & Engn, Bio Engn Lab, Basel, Switzerland..
Swiss Fed Inst Technol, Dept Biosyst Sci & Engn, Bio Engn Lab, Basel, Switzerland..
Show others and affiliations
2016 (English)In: Frontiers in Neuroscience, ISSN 1662-4548, E-ISSN 1662-453X, Vol. 10, 83Article in journal (Refereed) PublishedText
Abstract [en]

Mammalian cortical axons are extremely thin processes that are difficult to study as a result of their small diameter: they are too narrow to patch while intact, and super-resolution microscopy is needed to resolve single axons. We present a method for studying axonal physiology by pairing a high-density microelectrode array with a microfluidic axonal isolation device, and use it to study activity-dependent modulation of axonal signal propagation evoked by stimulation near the soma. Up to three axonal branches from a single neuron, isolated in different channels, were recorded from simultaneously using 10-20 electrodes per channel. The axonal channels amplified spikes such that propagations of individual signals along tens of electrodes could easily be discerned with high signal to noise. Stimulation from 10 up to 160 Hz demonstrated similar qualitative results from all of the cells studied: extracellular action potential characteristics changed drastically in response to stimulation. Spike height decreased, spike width increased, and latency increased, as a result of reduced propagation velocity, as the number of stimulations and the stimulation frequencies increased. Quantitatively, the strength of these changes manifested itself differently in cells at different frequencies of stimulation. Some cells' signal fidelity fell to 80% already at 10 Hz, while others maintained 80% signal fidelity at 80 Hz. Differences in modulation by axonal branches of the same cell were also seen for different stimulation frequencies, starting at 10 Hz. Potassium ion concentration changes altered the behavior of the cells causing propagation failures at lower concentrations and improving signal fidelity at higher concentrations.

Place, publisher, year, edition, pages
2016. Vol. 10, 83
Keyword [en]
microelectrode array, axon, axonal propagation, neuronal stimulation, axonal channels, electrophysiology
National Category
URN: urn:nbn:se:uu:diva-282804DOI: 10.3389/fnins.2016.00083ISI: 000371566000002PubMedID: 27013945OAI: diva2:919133
EU, European Research Council, AdG 267351
Available from: 2016-04-13 Created: 2016-04-07 Last updated: 2016-04-13Bibliographically approved

Open Access in DiVA

fulltext(5606 kB)40 downloads
File information
File name FULLTEXT01.pdfFile size 5606 kBChecksum SHA-512
Type fulltextMimetype application/pdf

Other links

Publisher's full textPubMed

Search in DiVA

By author/editor
Lewandowska, Marta K.
By organisation
Clinical Neurophysiology
In the same journal
Frontiers in Neuroscience

Search outside of DiVA

GoogleGoogle Scholar
Total: 40 downloads
The number of downloads is the sum of all downloads of full texts. It may include eg previous versions that are now no longer available

Altmetric score

Total: 63 hits
ReferencesLink to record
Permanent link

Direct link