Characterization of voltage-gated Ca(2+) conductances in layer 5 neocortical pyramidal neurons from rats.
Neuronal voltage-gated Ca(2+) channels are involved in electrical signalling and in converting these signals into cytoplasmic calcium changes. One important function of voltage-gated Ca(2+) channels is generating regenerative dendritic Ca(2+) spikes. However, the Ca(2+) dependent mechanisms used to...
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2009-01-01
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doaj-04ed304544e74087b361e407c220aa912021-03-03T22:40:50ZengPublic Library of Science (PLoS)PLoS ONE1932-62032009-01-0144e484110.1371/journal.pone.0004841Characterization of voltage-gated Ca(2+) conductances in layer 5 neocortical pyramidal neurons from rats.Mara AlmogAlon KorngreenNeuronal voltage-gated Ca(2+) channels are involved in electrical signalling and in converting these signals into cytoplasmic calcium changes. One important function of voltage-gated Ca(2+) channels is generating regenerative dendritic Ca(2+) spikes. However, the Ca(2+) dependent mechanisms used to create these spikes are only partially understood. To start investigating this mechanism, we set out to kinetically and pharmacologically identify the sub-types of somatic voltage-gated Ca(2+) channels in pyramidal neurons from layer 5 of rat somatosensory cortex, using the nucleated configuration of the patch-clamp technique. The activation kinetics of the total Ba(2+) current revealed conductance activation only at medium and high voltages suggesting that T-type calcium channels were not present in the patches. Steady-state inactivation protocols in combination with pharmacology revealed the expression of R-type channels. Furthermore, pharmacological experiments identified 5 voltage-gated Ca(2+) channel sub-types - L-, N-, R- and P/Q-type. Finally, the activation of the Ca(2+) conductances was examined using physiologically derived voltage-clamp protocols including a calcium spike protocol and a mock back-propagating action potential (mBPAP) protocol. These experiments enable us to suggest the possible contribution of the five Ca(2+) channel sub-types to Ca(2+) current flow during activation under physiological conditions.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/19337371/pdf/?tool=EBI |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mara Almog Alon Korngreen |
spellingShingle |
Mara Almog Alon Korngreen Characterization of voltage-gated Ca(2+) conductances in layer 5 neocortical pyramidal neurons from rats. PLoS ONE |
author_facet |
Mara Almog Alon Korngreen |
author_sort |
Mara Almog |
title |
Characterization of voltage-gated Ca(2+) conductances in layer 5 neocortical pyramidal neurons from rats. |
title_short |
Characterization of voltage-gated Ca(2+) conductances in layer 5 neocortical pyramidal neurons from rats. |
title_full |
Characterization of voltage-gated Ca(2+) conductances in layer 5 neocortical pyramidal neurons from rats. |
title_fullStr |
Characterization of voltage-gated Ca(2+) conductances in layer 5 neocortical pyramidal neurons from rats. |
title_full_unstemmed |
Characterization of voltage-gated Ca(2+) conductances in layer 5 neocortical pyramidal neurons from rats. |
title_sort |
characterization of voltage-gated ca(2+) conductances in layer 5 neocortical pyramidal neurons from rats. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2009-01-01 |
description |
Neuronal voltage-gated Ca(2+) channels are involved in electrical signalling and in converting these signals into cytoplasmic calcium changes. One important function of voltage-gated Ca(2+) channels is generating regenerative dendritic Ca(2+) spikes. However, the Ca(2+) dependent mechanisms used to create these spikes are only partially understood. To start investigating this mechanism, we set out to kinetically and pharmacologically identify the sub-types of somatic voltage-gated Ca(2+) channels in pyramidal neurons from layer 5 of rat somatosensory cortex, using the nucleated configuration of the patch-clamp technique. The activation kinetics of the total Ba(2+) current revealed conductance activation only at medium and high voltages suggesting that T-type calcium channels were not present in the patches. Steady-state inactivation protocols in combination with pharmacology revealed the expression of R-type channels. Furthermore, pharmacological experiments identified 5 voltage-gated Ca(2+) channel sub-types - L-, N-, R- and P/Q-type. Finally, the activation of the Ca(2+) conductances was examined using physiologically derived voltage-clamp protocols including a calcium spike protocol and a mock back-propagating action potential (mBPAP) protocol. These experiments enable us to suggest the possible contribution of the five Ca(2+) channel sub-types to Ca(2+) current flow during activation under physiological conditions. |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/19337371/pdf/?tool=EBI |
work_keys_str_mv |
AT maraalmog characterizationofvoltagegatedca2conductancesinlayer5neocorticalpyramidalneuronsfromrats AT alonkorngreen characterizationofvoltagegatedca2conductancesinlayer5neocorticalpyramidalneuronsfromrats |
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1714812328987328512 |