TY - JOUR
T1 - α1E-Containing Ca2+ channels are involved in synaptic plasticity
AU - Breustedt, J.
AU - Vogt, K. E.
AU - Miller, R. J.
AU - Nicoll, R. A.
AU - Schmitz, D.
PY - 2003/10/14
Y1 - 2003/10/14
N2 - Long-term potentiation (LTP) is the most prominent model for the molecular and cellular mechanisms of learning and memory. Two main forms of LTP have been distinguished. The N-methyl-D-aspartate-receptor-dependent forms of LTP have been studied most extensively, whereas much less is known about N-methyl-D-aspartate-receptor-independent forms of LTP. This latter type of LTP was first described at the mossy fiber synapses in the hippocampus and subsequently at parallel fiber synapses in the cerebellum as well as at corticothalamic synapses. These presynaptic forms of LTP require a rise in the intraterminal calcium concentration, but the channel through which calcium passes has not been identified. By using pharmacological tools as well as genetic deletion, we demonstrate here that α1E-containing voltage-dependent calcium channels (VDCCs) shift the threshold for mossy fiber LTP. The channel is not involved in the expression mechanism, but it contributes to the calcium influx during the induction phase. Indeed, optical recordings directly show the presence and the function of α 1E-containing VDCCs at mossy fiber terminals. Hence, a previously undescribed role for α1E-containing VDCCs is suggested by these results.
AB - Long-term potentiation (LTP) is the most prominent model for the molecular and cellular mechanisms of learning and memory. Two main forms of LTP have been distinguished. The N-methyl-D-aspartate-receptor-dependent forms of LTP have been studied most extensively, whereas much less is known about N-methyl-D-aspartate-receptor-independent forms of LTP. This latter type of LTP was first described at the mossy fiber synapses in the hippocampus and subsequently at parallel fiber synapses in the cerebellum as well as at corticothalamic synapses. These presynaptic forms of LTP require a rise in the intraterminal calcium concentration, but the channel through which calcium passes has not been identified. By using pharmacological tools as well as genetic deletion, we demonstrate here that α1E-containing voltage-dependent calcium channels (VDCCs) shift the threshold for mossy fiber LTP. The channel is not involved in the expression mechanism, but it contributes to the calcium influx during the induction phase. Indeed, optical recordings directly show the presence and the function of α 1E-containing VDCCs at mossy fiber terminals. Hence, a previously undescribed role for α1E-containing VDCCs is suggested by these results.
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U2 - 10.1073/pnas.2035117100
DO - 10.1073/pnas.2035117100
M3 - Article
C2 - 14519849
AN - SCOPUS:0142027741
SN - 0027-8424
VL - 100
SP - 12450
EP - 12455
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 21
ER -