Polyunsaturated fatty acids activate the Drosophila light-sensitive channels TRP and TRPL.
Nature
; 397(6716): 255-9, 1999 Jan 21.
Article
in En
| MEDLINE
| ID: mdl-9930700
Phototransduction in invertebrate microvillar photoreceptors is thought to be mediated by the activation of phospholipase C (PLC), but how this leads to gating of the light-sensitive channels is unknown. Most attention has focused on inositol-1,4,5-trisphosphate, a second messenger produced by PLC from phosphatidylinositol-4,5-bisphosphate; however, PLC also generates diacylglycerol, a potential precursor for several polyunsaturated fatty acids, such as arachidonic acid and linolenic acid. Here we show that both of these fatty acids reversibly activate native light-sensitive channels (transient receptor potential (TRP) and TRP-like (TRPL)) in Drosophila photoreceptors as well as recombinant TRPL channels expressed in Drosophila S2 cells. Recombinant channels are activated rapidly in both whole-cell recordings and inside-out patches, with a half-maximal effector concentration for linolenic acid of approximately 10 microM. Four different lipoxygenase inhibitors, which might be expected to lead to build-up of endogenous fatty acids, also activate native TRP and TRPL channels in intact photoreceptors. As arachidonic acid may not be found in Drosophila, we suggest that another polyunsaturated fatty acid, such as linolenic acid, may be a messenger of excitation in Drosophila photoreceptors.
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Calmodulin-Binding Proteins
/
Calcium Channels
/
Photoreceptor Cells, Invertebrate
/
Insect Proteins
/
Drosophila Proteins
/
Fatty Acids, Unsaturated
/
Membrane Proteins
Type of study:
Diagnostic_studies
Limits:
Animals
Language:
En
Journal:
Nature
Year:
1999
Document type:
Article
Country of publication:
United kingdom