Opposite developmental regulation of P- and Q-type calcium currents during ontogenesis of large diameter mouse sensory neurons

被引:24
作者
Hilaire, C
Diochot, S
Desmadryl, G
BaldyMoulinier, M
Richard, S
Valmier, J
机构
[1] INSERM, U249, INST BIOL, LAB MED EXPT, CNRS UPR 9008, F-34060 MONTPELLIER, FRANCE
[2] INSERM, U249, CTR RECH BIOCHIM MACROMOL, CNRS UPR 9008, F-34033 MONTPELLIER, FRANCE
[3] UNIV MONTPELLIER 2, INSERM, U432, LAB NEUROPHYSIOL SENSORIELLE, F-34095 MONTPELLIER 5, FRANCE
关键词
ontogenesis; calcium channels; whole-cell patch-clamp; conotoxin; agatoxin;
D O I
10.1016/0306-4522(96)00347-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Analysis of neuronal development has emphasized the importance of voltage-activated Ca2+ currents during the initial period of differentiation. We investigated non-N, non-L Ba2+ currents through Ca2+ channels in freshly dissociated large diameter embryonic mouse dorsal root ganglion neurons using the whole-cell patch-clamp technique. Two types of omega-agatoxin IVA-sensitive currents were clearly distinguished at embryonic day 13: a sustained P-type current blocked selectively at 30 nM (IC50=3 nM) and an inactivating Q-type current blocked in the range 50-500 nM (IC50=120 nM). The P-type Ca2+ current disappeared at day 15 whereas the Q-type Ca2+ current increased two- to three-fold during the same embryonic period. In contrast, the contribution of the non-L, non-N, omega-agatoxin IVA-resistant current (R-type) was constant during this developmental span. In conclusion, our results clearly show that P- and Q-type Ca2+ currents are differentially expressed during ontogenesis in large diameter dorsal root ganglion neurons. The developmental change, which occurs during the period of target innervation, could be related to specific key events such as natural neuron death and onset of synapse formation.
引用
收藏
页码:1219 / 1229
页数:11
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