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- Title
Myosin light chain kinase-independent inhibition by ML-9 of murine TRPC6 channels expressed in HEK293 cells.
- Authors
Shi, J.; Takahashi, S.; Jin, X.-H.; Li, Y.-Q.; Ito, Y.; Mori, Y.; Inoue, R.
- Abstract
Background and purpose:Myosin light chain kinase (MLCK) plays a pivotal role in regulation of cellular functions, the evidence often relying on the effects of extracelluarly administered drugs such as ML-9. Here we report that this compound exerts non-specific inhibitory actions on the TRPC6 channel, a transient receptor potential (TRP) protein.Experimental approach:Macroscopic and single channel currents were recorded from transfected HEK293 cells by patch-clamp techniques.Key results:Cationic currents elicited by carbachol (CCh; 100 μM) in HEK293 cells overexpressing murine TRPC6 (ITRPC6) were dose-dependently inhibited by externally applied ML-9 (IC50=7.8 μM). This inhibition was voltage-dependent and occurred as fast as external Na+ removal. Another MLCK inhibitor, wortmannin (3 μM), and MLCK inhibitory peptides MLCK-IP11-19 (10 μM) and -IP480-501 (1 μM) showed little effects on ITRPC6 density and the inhibitory efficacy of ML-9. The extent of the inhibition also unchanged with co-expression of wild-type or a dominant negative mutant of MLCK. Inhibitory effects of ML-9 on ITRPC6 remained unaffected whether TRPC6 was activated constitutively or by a diacylglycerol analogue OAG (100 μM). Similar rapid inhibition was also observed with a ML-9 relative, ML-7. Intracellular perfusion of ML-9 via patch pipette, dose-dependently suppressed ITRPC6. In inside-out patch configuration, bath application of ML-9 (and ML-7) rapidly diminished ∼35pS single TRPC6 channel activities. Contrarily, currents due to TRPC7 expression were rapidly enhanced by externally applied ML-9 and ML-7, which was not prevented by MLCK inhibitory peptides.Conclusion and implications:These results strongly suggest that ML compounds inhibit TRPC6 channels via a mechanism independent of inhibition of MLCK activity.British Journal of Pharmacology (2007) 152, 122–131; doi:10.1038/sj.bjp.0707368; published online 2 July 2007
- Subjects
MYOSIN; CELLULAR control mechanisms; TRP channels; NAPHTHALENE; CATION metabolism; CALMODULIN
- Publication
British Journal of Pharmacology, 2007, Vol 152, Issue 1, p122
- ISSN
0007-1188
- Publication type
Article
- DOI
10.1038/sj.bjp.0707368