Optopharmacological control of TRPC channels by coumarin-caged lipids is associated with a phototoxic membrane effect
Autor: | Gema Guedes de la Cruz, Klaus Groschner, Oleksandra Tiapko, Bernadett Bacsa, Toma N. Glasnov |
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Rok vydání: | 2016 |
Předmět: |
0301 basic medicine
Cell signaling Patch-Clamp Techniques Ultraviolet Rays General Biochemistry Genetics and Molecular Biology Membrane Potentials Diglycerides 03 medical and health sciences Environmental Science(all) Coumarins Humans Calcium Signaling Ion channel TRPC TRPC Cation Channels General Environmental Science Calcium signaling Membrane potential Photolysis Agricultural and Biological Sciences(all) Biochemistry Genetics and Molecular Biology(all) Chemistry Imidazoles Lipid signaling Calcium Channel Blockers Lipids Luminescent Proteins HEK293 Cells 030104 developmental biology Microscopy Fluorescence Second messenger system Biophysics Calcium General Agricultural and Biological Sciences Signal Transduction |
Zdroj: | Science China Life Sciences. 59:802-810 |
ISSN: | 1869-1889 1674-7305 |
DOI: | 10.1007/s11427-016-5095-5 |
Popis: | Photouncaging of second messengers has been successfully employed to gain mechanistic insight of cellular signaling pathways. One of the most enigmatic processes of ion channel regulation is lipid recognition and lipid-gating of TRPC channels, which represents pivotal mechanisms of cellular Ca(2+) homeostasis. Recently, optopharmacological tools including caged lipid mediators became available, enabling an unprecedented level of temporal and spatial control of the activating lipid species within a cellular environment. Here we tested a commonly used caged ligand approach for suitability to investigate TRPC signaling at the level of membrane conductance and cellular Ca(2+) handling. We report a specific photouncaging artifact that is triggered by the cage structure coumarin at UV illumination. Electrophysiological characterization identified a light-dependent membrane effect of coumarin. UV light (340 nm) as used for photouncaging, initiated a membrane conductance specifically in the presence of coumarin as low as 30 μmol L(-1) concentrations. This conductance masked the TRPC3 conductance evoked by photouncaging, while TRPC-mediated cellular Ca(2+) responses were largely preserved. The observed light-induced membrane effects of the released caging moiety may well interfere with certain cellular functions, and prompt caution in using coumarin-caged second messengers in cellular studies. |
Databáze: | OpenAIRE |
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