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Molecular characterization of T-type Ca2+ channels responsible for low threshold spikes in hypothalamic paraventricular nucleus neurons

  • S. Lee
    ,
  • T. H. Han
    ,
  • P. M. Sonner
    ,
  • Javier Eduardo Stern
    ,
  • P. D. Ryu
    ,
  • S. Y. Lee(corresponding author)
*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

The hypothalamic paraventricular nucleus (PVN) is composed of functionally heterogeneous cell groups, possessing distinct electrophysiological properties depending on their functional roles. Previously, T-type Ca2+ dependent low-threshold spikes (LTS) have been demonstrated in various PVN neuronal types, including preautonomic cells. However, the molecular composition and functional properties of the underlying T-type Ca2+ channels have not been characterized. In the present study, we combined single cell reverse transcription-polymerase chain reaction (RT-PCR), immunohistochemistry and patch-clamp recordings to identify subtypes of T-type Ca2+ channels expressed in PVN cells displaying LTS (PVN-LTS), including identified preautonomic neurons. LTS appeared at the end of hyperpolarizing pulses either as long-lasting plateaus or as short-lasting depolarizing humps. LTS were mediated by rapidly activating and inactivating T-type Ca2+ currents and were blocked by Ni2+. Single cell RT-PCR and immunohistochemical studies revealed Cav3.1 (voltage-gated Ca2+ channel) as the main channel subunit detected in PVN-LTS neurons. In conclusion, these data indicate that Cav3.1 is the major subtype of T-type Ca2+ channel subunit that mediates T-type Ca2+ dependent LTS in PVN neurons.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 1195-1203 (9 pages)

Journal (Volume, Issue Number)

Neuroscience (Volume 155, Issue 4)

Publication milestones

  • Published - 09/09/2008

Publication status

Published - 09/09/2008

ISSN

0306-4522

Publication IDs

  • Scopus: 50249142941
  • PubMed: 18657597

Publication metrics

Metrics

Scopus
citations
SciVal
citations
18
SciVal
FWCI
0.42
SciVal
Author count
6
SciVal
Paper percentile
72
Fractional count
1
Fractional count
0.17
Fractional count
5
Fractional count
0.83
Fractional count
1
Fractional count
1

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Citation count
17
Captures
26

Funding Details

This work was supported by a Korea Research Foundation Grant funded by the Korean government (MOEHRD, Basic Research Promotion Fund) (KRF-2006-331-E00349) to S.Y.L. and by NIH RO1 HL 68725 to J.E.S.
FundersFunding numbers
National Research Foundation of Korea
-
NIH
-
NHLBI
R01HL068725
MOEHRD
KRF-2006-331-E00349