Dendritic a-current in rhythmically active prebötzinger complex neurons in organotypic cultures from Newborn mice

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Dendritic a-current in rhythmically active prebötzinger complex neurons in organotypic cultures from Newborn mice. / Phillips, Wiktor S.; Del Negro, Christopher A.; Rekling, Jens C.

In: Journal of Neuroscience, Vol. 38, No. 12, 2018, p. 3039-3049.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Phillips, WS, Del Negro, CA & Rekling, JC 2018, 'Dendritic a-current in rhythmically active prebötzinger complex neurons in organotypic cultures from Newborn mice', Journal of Neuroscience, vol. 38, no. 12, pp. 3039-3049. https://doi.org/10.1523/JNEUROSCI.3342-17.2018

APA

Phillips, W. S., Del Negro, C. A., & Rekling, J. C. (2018). Dendritic a-current in rhythmically active prebötzinger complex neurons in organotypic cultures from Newborn mice. Journal of Neuroscience, 38(12), 3039-3049. https://doi.org/10.1523/JNEUROSCI.3342-17.2018

Vancouver

Phillips WS, Del Negro CA, Rekling JC. Dendritic a-current in rhythmically active prebötzinger complex neurons in organotypic cultures from Newborn mice. Journal of Neuroscience. 2018;38(12):3039-3049. https://doi.org/10.1523/JNEUROSCI.3342-17.2018

Author

Phillips, Wiktor S. ; Del Negro, Christopher A. ; Rekling, Jens C. / Dendritic a-current in rhythmically active prebötzinger complex neurons in organotypic cultures from Newborn mice. In: Journal of Neuroscience. 2018 ; Vol. 38, No. 12. pp. 3039-3049.

Bibtex

@article{b0609e97a55e4a72a868b31a39e54a1f,
title = "Dendritic a-current in rhythmically active preb{\"o}tzinger complex neurons in organotypic cultures from Newborn mice",
abstract = "The brainstem preB{\"o}tzinger complex (preB{\"o}tC) generates the inspiratory rhythm for breathing. The onset of neural activity that precipitates the inspiratory phase of the respiratory cycle may depend on the activity of type-1 preB{\"o}tC neurons, which exhibit a transient outward K+ current, IA. Inspiratory rhythm generation can be studied ex vivo because the preB{\"o}tC remains rhythmically active in vitro, both in acute brainstem slices and organotypic cultures. Advantageous optical conditions in organotypic slice cultures from newborn mice of either sex allowed us to investigate how IA impacts Ca2+ transients occurring in the dendrites of rhythmically active type-1 preB{\"o}tC neurons. The amplitude of dendritic Ca2+ transients evoked via voltage increases originating from the soma significantly increased after an IA antagonist, 4-aminopyridine (4-AP), was applied to the perfusion bath or to local dendritic regions. Similarly, glutamate-evoked postsynaptic depolarizations recorded at the soma increased in amplitude when 4-AP was coapplied with glutamate at distal dendritic locations. We conclude that IA is expressed on type-1 preB{\"o}tC neuron dendrites. We propose that IA filters synaptic input, shunting sparse excitation, while enabling temporally summated events to pass more readily as a result of IA inactivation. Dendritic IA in rhythmically active preB{\"o}tC neurons could thus ensure that inspiratory motor activity does not occur until excitatory synaptic drive is synchronized and well coordinated among cellular constituents of the preB{\"o}tC during inspiratory rhythmogenesis. The biophysical properties of dendritic IA might thus promote robustness and regularity of breathing rhythms.",
keywords = "A-current, Breathing, Dendrites, Potassium channels, PreB{\"o}tzinger, Respiratory neurons",
author = "Phillips, {Wiktor S.} and {Del Negro}, {Christopher A.} and Rekling, {Jens C.}",
year = "2018",
doi = "10.1523/JNEUROSCI.3342-17.2018",
language = "English",
volume = "38",
pages = "3039--3049",
journal = "The Journal of neuroscience : the official journal of the Society for Neuroscience",
issn = "0270-6474",
publisher = "Society for Neuroscience",
number = "12",

}

RIS

TY - JOUR

T1 - Dendritic a-current in rhythmically active prebötzinger complex neurons in organotypic cultures from Newborn mice

AU - Phillips, Wiktor S.

AU - Del Negro, Christopher A.

AU - Rekling, Jens C.

PY - 2018

Y1 - 2018

N2 - The brainstem preBötzinger complex (preBötC) generates the inspiratory rhythm for breathing. The onset of neural activity that precipitates the inspiratory phase of the respiratory cycle may depend on the activity of type-1 preBötC neurons, which exhibit a transient outward K+ current, IA. Inspiratory rhythm generation can be studied ex vivo because the preBötC remains rhythmically active in vitro, both in acute brainstem slices and organotypic cultures. Advantageous optical conditions in organotypic slice cultures from newborn mice of either sex allowed us to investigate how IA impacts Ca2+ transients occurring in the dendrites of rhythmically active type-1 preBötC neurons. The amplitude of dendritic Ca2+ transients evoked via voltage increases originating from the soma significantly increased after an IA antagonist, 4-aminopyridine (4-AP), was applied to the perfusion bath or to local dendritic regions. Similarly, glutamate-evoked postsynaptic depolarizations recorded at the soma increased in amplitude when 4-AP was coapplied with glutamate at distal dendritic locations. We conclude that IA is expressed on type-1 preBötC neuron dendrites. We propose that IA filters synaptic input, shunting sparse excitation, while enabling temporally summated events to pass more readily as a result of IA inactivation. Dendritic IA in rhythmically active preBötC neurons could thus ensure that inspiratory motor activity does not occur until excitatory synaptic drive is synchronized and well coordinated among cellular constituents of the preBötC during inspiratory rhythmogenesis. The biophysical properties of dendritic IA might thus promote robustness and regularity of breathing rhythms.

AB - The brainstem preBötzinger complex (preBötC) generates the inspiratory rhythm for breathing. The onset of neural activity that precipitates the inspiratory phase of the respiratory cycle may depend on the activity of type-1 preBötC neurons, which exhibit a transient outward K+ current, IA. Inspiratory rhythm generation can be studied ex vivo because the preBötC remains rhythmically active in vitro, both in acute brainstem slices and organotypic cultures. Advantageous optical conditions in organotypic slice cultures from newborn mice of either sex allowed us to investigate how IA impacts Ca2+ transients occurring in the dendrites of rhythmically active type-1 preBötC neurons. The amplitude of dendritic Ca2+ transients evoked via voltage increases originating from the soma significantly increased after an IA antagonist, 4-aminopyridine (4-AP), was applied to the perfusion bath or to local dendritic regions. Similarly, glutamate-evoked postsynaptic depolarizations recorded at the soma increased in amplitude when 4-AP was coapplied with glutamate at distal dendritic locations. We conclude that IA is expressed on type-1 preBötC neuron dendrites. We propose that IA filters synaptic input, shunting sparse excitation, while enabling temporally summated events to pass more readily as a result of IA inactivation. Dendritic IA in rhythmically active preBötC neurons could thus ensure that inspiratory motor activity does not occur until excitatory synaptic drive is synchronized and well coordinated among cellular constituents of the preBötC during inspiratory rhythmogenesis. The biophysical properties of dendritic IA might thus promote robustness and regularity of breathing rhythms.

KW - A-current

KW - Breathing

KW - Dendrites

KW - Potassium channels

KW - PreBötzinger

KW - Respiratory neurons

U2 - 10.1523/JNEUROSCI.3342-17.2018

DO - 10.1523/JNEUROSCI.3342-17.2018

M3 - Journal article

C2 - 29459371

AN - SCOPUS:85044349243

VL - 38

SP - 3039

EP - 3049

JO - The Journal of neuroscience : the official journal of the Society for Neuroscience

JF - The Journal of neuroscience : the official journal of the Society for Neuroscience

SN - 0270-6474

IS - 12

ER -

ID: 202427213