TY - JOUR
T1 - Signaling role of the voltage-gated calcium channel as the molecular on/off-switch of secretion
AU - Atlas, Daphne
PY - 2010/11
Y1 - 2010/11
N2 - Voltage-gated calcium channels (VGCC) are involved in a large variety of cellular Ca2+ signaling processes, including exocytosis, a Ca2+ dependent release of neurotransmitters and hormones.Great progress has been made in understanding the mode of action of VGCC in exocytosis, a process distinguished by two sequential yet independent Ca2+ binding reactions. First, Ca2+ binds at the selectivity filter, the EEEE motif of the VGCC, and second, subsequent to a brief and intense Ca2+ inflow to synaptotagmin, a vesicular protein. Inquiry into the functional and physical interactions of the channels with synaptic proteins has demonstrated that exocytosis is triggered during the initial Ca2+ binding at the channel pore, prior to Ca2+ entry. Accordingly, a cycle of secretion begins by an incoming stimulus that releases vesicles from a releasable pool upon Ca2+ binding at the pore, and at the same time, the transient increase in [Ca2+]i primes a fresh set of non-releasable vesicles, to be fused by the next incoming stimulus.We propose a model, in which the Ca2+ binding at the EEEE motif and the consequent conformational changes in the channel are the primary event in triggering secretion, while synaptotagmin acts as a vesicle docking protein. Thus, the channel serves as the molecular On/Off signaling switch, where the predominance of a conformational change in Ca2+-bound channel provides for the fast secretory process.
AB - Voltage-gated calcium channels (VGCC) are involved in a large variety of cellular Ca2+ signaling processes, including exocytosis, a Ca2+ dependent release of neurotransmitters and hormones.Great progress has been made in understanding the mode of action of VGCC in exocytosis, a process distinguished by two sequential yet independent Ca2+ binding reactions. First, Ca2+ binds at the selectivity filter, the EEEE motif of the VGCC, and second, subsequent to a brief and intense Ca2+ inflow to synaptotagmin, a vesicular protein. Inquiry into the functional and physical interactions of the channels with synaptic proteins has demonstrated that exocytosis is triggered during the initial Ca2+ binding at the channel pore, prior to Ca2+ entry. Accordingly, a cycle of secretion begins by an incoming stimulus that releases vesicles from a releasable pool upon Ca2+ binding at the pore, and at the same time, the transient increase in [Ca2+]i primes a fresh set of non-releasable vesicles, to be fused by the next incoming stimulus.We propose a model, in which the Ca2+ binding at the EEEE motif and the consequent conformational changes in the channel are the primary event in triggering secretion, while synaptotagmin acts as a vesicle docking protein. Thus, the channel serves as the molecular On/Off signaling switch, where the predominance of a conformational change in Ca2+-bound channel provides for the fast secretory process.
KW - Ca channel
KW - Ca sensor
KW - Depolarization-evoked secretion
KW - Exocytosis
KW - L-type channel
KW - Synaptic transmission
UR - http://www.scopus.com/inward/record.url?scp=77955657644&partnerID=8YFLogxK
U2 - 10.1016/j.cellsig.2010.04.003
DO - 10.1016/j.cellsig.2010.04.003
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C2 - 20388539
AN - SCOPUS:77955657644
SN - 0898-6568
VL - 22
SP - 1597
EP - 1603
JO - Cellular Signalling
JF - Cellular Signalling
IS - 11
ER -