Referenced in: none

Automatically associated channels: TRP

Title: TRP-ML1 functions as a lysosomal NAADP-sensitive Ca2+ release channel in coronary arterial myocytes.

Authors: Fan Zhang, Si Jin, Fan Yi, Pin-Lan Li

Journal, date & volume: J. Cell. Mol. Med., 2009 Sep , 13, 3174-85

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/18754814

Abstract
Nicotinic acid adenine dinucleotide phosphate (NAADP) is a potent intracellular Ca(2+) signalling second messenger, but the mechanism of NAADP-induced Ca(2+) release is still poorly understood. The present study tested the hypothesis that NAADP induces Ca(2+) release from the lysosomal store via a TRP-ML1 (transient receptor potential-mucolipin 1)-mediated Ca(2+) release channel in coronary arterial myocytes (CAMs). RT-PCR and Western blot analyses demonstrated that TRP-ML1 was present in CAMs, and fluorescence resonance energy transfer (FRET) detection revealed that the TRP-ML1 was closely associated with some lysosomal proteins in these CAMs. ET-1, a well-known NAADP stimulator, was found to induce a local Ca(2+) burst from lysosomes followed by a global Ca(2+) release. This lysosome-associated Ca(2+) release was significantly inhibited in the TRP-ML1 siRNA pre-treated CAMs by 46.8 +/- 12.6% in the local Ca(2+) burst and 73.3 +/- 14.9% in the global Ca(2+) wave. In the reconstituted lysosomal channels from CAMs, NAADP activated Ca(2+) release channels at concentrations of 1-1000 nM, but neither activators (1 microM IP(3), 5 microM Rya) nor blockers (100 microM 2-APB, 50 microM Rya) of sarcoplasmic reticulum (SR) Ca(2+) release channels had effect on the channel activity. Moreover, TRP-ML1 gene silencing reduced this NAADP-sensitive Ca(2+) release channel activity in lysosomes by 71.5 +/- 18.5%. Immunoprecipitation or blockade of TRP-ML1 by anti-TRP-ML1 antibodies almost abolished NAADP-induced activation of lysosomal Ca(2+) channels (to 14.0 +/- 4.4% of control). These results for the first time provide direct evidence that an NAADP-sensitive Ca(2+) release channel is characteristic of TRP-ML1 channels.