A defined heteromeric KV1 channel stabilizes the intrinsic pacemaking and regulates the output of deep cerebellar nuclear neurons to thalamic targets. (19th February 2013)
- Record Type:
- Journal Article
- Title:
- A defined heteromeric KV1 channel stabilizes the intrinsic pacemaking and regulates the output of deep cerebellar nuclear neurons to thalamic targets. (19th February 2013)
- Main Title:
- A defined heteromeric KV1 channel stabilizes the intrinsic pacemaking and regulates the output of deep cerebellar nuclear neurons to thalamic targets
- Authors:
- Ovsepian, Saak V.
Steuber, Volker
Le Berre, Marie
O'Hara, Liam
O'Leary, Valerie B.
Dolly, J. Oliver - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Key points</title> <p> <list id="l1" list-type="simple"> <list-item> <label> </label> <p>The result of cerebellar integration is encoded in the output of deep cerebellar nuclear (DCN) neurons in the form of dynamic changes in spontaneous firing rate and pattern.</p> </list-item> <list-item> <label> </label> <p>The soma of these neurons has been demonstrated to be enriched with potassium channels (K<sub>V</sub>1) produced by mandatory multi‐merization of K<sub>V</sub>1.1, 1.2 α and K<sub>V</sub>β2 subunits.</p> </list-item> <list-item> <label> </label> <p>The outward K<sup>+</sup> current (<italic>I</italic>K<sub>V</sub>1) mediated by these channels is proven to be a critical stabilizer for both the rate and temporal precision of self‐sustained firing of DCN neurons.</p> </list-item> <list-item> <label> </label> <p>Activated from low‐threshold, <italic>I</italic>K<sub>V</sub>1 provides an effective counter‐balance to depolarizing inputs, attenuates the back‐propagating action potentials, favouring dominance of clock‐like somatic pace‐making of these cells – an important condition for accurate encoding of time variant inputs.</p> </list-item> <list-item> <label> </label> <p>The relevance of these observations to physiology and integrative brain mechanisms is shown through a multi‐compartmental neuronal model as well as retro‐axonal tracing of neurons projecting to thalamic relay nuclei.</p> </list-item> </list> </p> <p><abstract abstract-type="main" xml:lang="en"> <title>Key points</title> <p> <list id="l1" list-type="simple"> <list-item> <label> </label> <p>The result of cerebellar integration is encoded in the output of deep cerebellar nuclear (DCN) neurons in the form of dynamic changes in spontaneous firing rate and pattern.</p> </list-item> <list-item> <label> </label> <p>The soma of these neurons has been demonstrated to be enriched with potassium channels (K<sub>V</sub>1) produced by mandatory multi‐merization of K<sub>V</sub>1.1, 1.2 α and K<sub>V</sub>β2 subunits.</p> </list-item> <list-item> <label> </label> <p>The outward K<sup>+</sup> current (<italic>I</italic>K<sub>V</sub>1) mediated by these channels is proven to be a critical stabilizer for both the rate and temporal precision of self‐sustained firing of DCN neurons.</p> </list-item> <list-item> <label> </label> <p>Activated from low‐threshold, <italic>I</italic>K<sub>V</sub>1 provides an effective counter‐balance to depolarizing inputs, attenuates the back‐propagating action potentials, favouring dominance of clock‐like somatic pace‐making of these cells – an important condition for accurate encoding of time variant inputs.</p> </list-item> <list-item> <label> </label> <p>The relevance of these observations to physiology and integrative brain mechanisms is shown through a multi‐compartmental neuronal model as well as retro‐axonal tracing of neurons projecting to thalamic relay nuclei.</p> </list-item> </list> </p> <p> <bold>Abstract </bold> The output of the cerebellum to the motor axis of the central nervous system is orchestrated mainly by synaptic inputs and intrinsic pacemaker activity of deep cerebellar nuclear (DCN) projection neurons. Herein, we demonstrate that the soma of these cells is enriched with K<sub>V</sub>1 channels produced by mandatory multi‐merization of K<sub>V</sub>1.1, 1.2 α and K<sub>V</sub>β2 subunits. Being constitutively active, the K<sup>+</sup> current (<italic>I</italic>K<sub>V</sub>1) mediated by these channels stabilizes the rate and regulates the temporal precision of self‐sustained firing of these neurons. Placed strategically, <italic>I</italic>K<sub>V</sub>1 provides a powerful counter‐balance to prolonged depolarizing inputs, attenuates the rebound excitation, and dampens the membrane potential bi‐stability. Somatic location with low activation threshold render <italic>I</italic>K<sub>V</sub>1 instrumental in voltage‐dependent de‐coupling of the axon initial segment from the cell body of projection neurons, impeding invasion of back‐propagating action potentials into the somato‐dendritic compartment. The latter is also demonstrated to secure the dominance of clock‐like somatic pacemaking in driving the regenerative firing activity of these neurons, to encode time variant inputs with high fidelity. Through the use of multi‐compartmental modelling and retro‐axonal labelling, the physiological significance of the described functions for processing and communication of information from the lateral DCN to thalamic relay nuclei is established.</p> </abstract> … (more)
- Is Part Of:
- Journal of physiology. Volume 591:Number 7(2013:Apr.)
- Journal:
- Journal of physiology
- Issue:
- Volume 591:Number 7(2013:Apr.)
- Issue Display:
- Volume 591, Issue 7 (2013)
- Year:
- 2013
- Volume:
- 591
- Issue:
- 7
- Issue Sort Value:
- 2013-0591-0007-0000
- Page Start:
- 1771
- Page End:
- 1791
- Publication Date:
- 2013-02-19
- Subjects:
- Physiology -- Periodicals
612.005 - Journal URLs:
- http://jp.physoc.org/ ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1113/jphysiol.2012.249706 ↗
- Languages:
- English
- ISSNs:
- 0022-3751
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5039.000000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4361.xml