ReviewCerebellum (London, England)2003
What are the roles of the many different types of potassium channel expressed in cerebellar granule cells?
Review in Cerebellum (London, England), 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.
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Who cites it
22 citing papers in PubMed, 50 citations in OpenAlex.
- Characterizing molecular and behavioral changes arising from ROMK potassium channel deficiency in the cerebellum.Frontiers in behavioral neuroscience · 2025Article
- A Direct Interaction between Cyclodextrins and TASK Channels Decreases the Leak Current in Cerebellar Granule Neurons.Biology · 2022Article
- Altered Sodium and Potassium, but not Calcium Currents in Cerebellar Granule Cells in an In Vitro Model of Neuronal Injury.Cellular and molecular neurobiology · 2017Article
- Typical gray matter axons in mammalian brain fail to conduct action potentials faithfully at fever-like temperatures.Physiological reports · 2016Article
- KV 10.1 opposes activity-dependent increase in Ca²⁺ influx into the presynaptic terminal of the parallel fibre-Purkinje cell synapse.The Journal of physiology · 2015Article
- Components of action potential repolarization in cerebellar parallel fibres.The Journal of physiology · 2014Article
- Neuregulin-1/ErbB4 signaling regulates Kv4.2-mediated transient outward K+ current through the Akt/mTOR pathway.American journal of physiology. Cell physiology · 2013Article
- Neuritin activates insulin receptor pathway to up-regulate Kv4.2-mediated transient outward K+ current in rat cerebellar granule neurons.The Journal of biological chemistry · 2012Article
- Models of calcium dynamics in cerebellar granule cells.Cerebellum (London, England) · 2012Review
- Mechanisms of ethanol-induced death of cerebellar granule cells.Cerebellum (London, England) · 2012Review
- Effects of calretinin on Ca2+ signals in cerebellar granule cells: implications of cooperative Ca2+ binding.Cerebellum (London, England) · 2012Article
- Receptor and channel heteromers as pain targets.Pharmaceuticals (Basel, Switzerland) · 2012Article
- Biophysical properties of human medulloblastoma cells.The Journal of membrane biology · 2010Article
- Article
- Neonatal diabetes mellitus.Endocrine reviews · 2008Review
- Ternary Kv4.2 channels recapitulate voltage-dependent inactivation kinetics of A-type K+ channels in cerebellar granule neurons.The Journal of physiology · 2008Article
- Identification of a region in the TASK3 two pore domain potassium channel that is critical for its blockade by methanandamide.British journal of pharmacology · 2007Article
- Neuronal two-pore-domain potassium channels and their regulation by G protein-coupled receptors.The Journal of physiology · 2007Review
- Modifying the subunit composition of TASK channels alters the modulation of a leak conductance in cerebellar granule neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2005Article
- Functional properties and pharmacological inhibition of ASIC channels in the human SJ-RH30 skeletal muscle cell line.The Journal of physiology · 2005Article
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Potassium (K) channels have a key role in the regulation of neuronal excitability. Over a hundred different subunits encoding distinct K channel subtypes have been identified so far. A major challenge is to relate these many different channel subunits to the functional K currents observed in native neurons. In this review, we have concentrated on cerebellar granule neurons (CGNs). We have considered each of the three principal super families of K channels in turn, namely, the six transmembrane domain, voltage-gated super family, the two transmembrane domain, inward-rectifier super family and the four transmembrane domain, leak channel super family. For each super family, we have identified the subunits that are expressed in CGNs and related the properties of these expressed channel subunits to the functional currents seen in electrophysiological recordings from these neurons. In some cases, there are strong molecular candidates for proteins underlying observed currents. In other cases the correlation is less clear. We show that at least 26 potassium channel alpha subunits are moderately or strongly expressed in CGNs. Nevertheless, a good empirical model of CGN function has been obtained with just six distinct K conductances. The transient KA current in CGNs, seems due to expression of Kv4.2 channels or Kv4.2/4.3 heteromers, while the KCa current is due to expression of large-conductance slo channels. The G-protein activated KIR current is probably due to heteromeric expression of KIR3.1 and KIR3.2. Perhaps KIR2.2 subunits underlie the KIR current when it is constitutively active. The leak conductance can be attributed to TASK-1 and or TASK-3 channels. With less certainty, the IK-slow current may be due to expression of one or more members of the KCNQ or EAG family. Lastly, the delayed-rectifier Kv current has as many as six different potential contributors from the extensive Kv family of alpha subunits. Since many of these subunits are highly regulated by neurotransmitters, physiological regulators and, often, auxiliary subunits, the resulting electrical properties of CGNs may be highly dynamic and subject to constant fine-tuning.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.