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Honeybee locomotion is impaired by Am-CaV3 low voltage-activated Ca2+ channel antagonist
Voltage‐gated Ca 2+ channels are key transducers of cellular excitability and participate in several crucial physiological responses. In vertebrates, 10 Ca 2+ channel genes, grouped in 3 families ( Ca V 1, Ca V 2 and Ca V 3 ), have been described and characterized. Insects possess only one member of...
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Published in: | Scientific reports 2017-02, Vol.7 (1), p.41782, Article 41782 |
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Main Authors: | , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Voltage‐gated Ca
2+
channels are key transducers of cellular excitability and participate in several crucial physiological responses. In vertebrates, 10 Ca
2+
channel genes, grouped in 3 families (
Ca
V
1, Ca
V
2
and
Ca
V
3
), have been described and characterized. Insects possess only one member of each family. These genes have been isolated in a limited number of species and very few have been characterized although, in addition to their crucial role, they may represent a collateral target for neurotoxic insecticides. We have isolated the 3 genes coding for the 3 Ca
2+
channels expressed in
Apis mellifera
. This work provides the first detailed characterization of the honeybee T-type Ca
V
3 Ca
2+
channel and demonstrates the low toxicity of inhibiting this channel. Comparing Ca
2+
currents recorded in bee neurons and myocytes with Ca
2+
currents recorded in Xenopus oocytes expressing the honeybee
Ca
V
3
gene suggests native expression in bee muscle cells only. High‐voltage activated Ca
2+
channels could be recorded in the somata of different cultured bee neurons. These functional data were confirmed by
in situ
hybridization, immunolocalization and
in vivo
analysis of the effects of a Ca
V
3 inhibitor. The biophysical and pharmacological characterization and the tissue distribution of Ca
V
3 suggest a role in honeybee muscle function. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/srep41782 |