The capsaicin receptor TRPV1, a member of the transient receptor potential family of non-selective cation channels is a polymodal nociceptor. Noxious thermal stimuli, protons, and the alkaloid irritant capsaicin open the channel. The mechanisms of heat and capsaicin activation have been linked to voltage-dependent gating in TRPV1. However, until now it was unclear whether proton activation or potentiation or both are linked to a similar voltagedependent mechanism and which molecular determinants underlie the proton gating. Using the whole-cell patchclamp technique, we show that protons activate and potentiate TRPV1 by shifting the voltage dependence of the activation curves towards more physiological membrane potentials. We further identified a key residue within the pore region of TRPV1, F660, to be critical for voltage-dependent proton activation and potentiation. We conclude that proton activation and potentiation of TRPV1 are both voltage dependent and that amino acid 660 is essential for proton-mediated gating of TRPV1.
Mast cells rely on Ca2+ signaling to initiate activation programs leading to release of proinflammatory mediators. The interplay between Ca2+ release from internal stores and Ca2+ entry through store-operated Ca2+ channels has been extensively studied. Using rat basophilic leukemia (RBL) mast cells and murine bone marrow-derived mast cells, we examine the role of Na+/Ca2+ exchangers. Calcium imaging experiments and patch clamp current recordings revealed both K+-independent and K+-dependent components of Na+/Ca2+ exchange. Northern blot analysis indicated the predominant expression of the K+-dependent sodium-calcium exchanger NCKX3. Transcripts of the exchangers NCX3 and NCKX1 were additionally detected in RBL cells with RT-PCR. The Ca2+ clearance via Na+/Ca2+ exchange represented ∼50% of the total clearance when Ca2+ signals reached levels ≥200 nM. Ca2+ signaling and store-operated Ca2+ entry were strongly reduced by inverting the direction of Na+/Ca2+ exchange, indicating that Na+/Ca2+ exchangers normally extrude Ca2+ ions from cytosol and prevent the Ca2+-dependent inactivation of store-operated Ca2+ channels. Working in the Ca2+ efflux mode, Na+/Ca2+ exchangers such as NCKX3 and NCX3 might, therefore, play a role in the Ag-induced mast cell activation by controlling the sustained phase of Ca2+ mobilization.
The precise temperature control of the ABI Prism 7900HT Sequence Detection System designed for detection of fluorescence of a biological sample in real-time PCR assays (TaqMan assays) was used to activate Thermo-TRP ion channels, enabling a novel 384-/96-well plate-based assay. Functional pharmacology was verified against the temperature activation using intracellular calcium fluorescence as a measure of ion channel activity. The assay is applicable to both heterologous expression systems and dorsal root ganglia primary cells. This will benefit several analgesic drug discovery programs searching for new Thermo-TRP modulators. (Journal of Biomolecular Screening 2009:662-667)
Using Rho GTPases-inhibiting clostridial cytotoxins, we showed recently in RBL cells that the GTPase Rac is involved in Fc⑀RI (high-affinity receptor for IgE) signaling and receptormediated calcium mobilization, including influx via calcium release-activated calcium channels. Here, we studied the role of Rho GTPases in muscarinic M1 receptor signaling in RBL 2H3-hm1 cells. Clostridium difficile toxin B, which inactivates Rho, Rac, and Cdc42, and Clostridium sordellii lethal toxin, which inhibits Rac but not Rho, blocked M1-mediated exocytosis, indicating that Rac but not Rho is involved in the regulation of receptor-mediated exocytosis. Although antigen-induced Fc⑀RI stimulation caused tyrosine phosphorylation of the Rac guanine nucleotide exchange factor Vav, M1 stimulation by carbachol activated Rac independently of Vav. The Rac-inactivating toxins blocked M1 receptor-induced membrane translocation of the pleckstrin homology domain of protein kinase B, which is a phosphoinositide 3-kinase effector. The M1-induced calcium release from internal stores was not affected by toxin B; however, the subsequent calcium influx from the extracellular space was inhibited. The data suggest that besides capacitative calcium entry, the M1 signaling pathway activates further calcium entry channels with mechanisms that are not affected by the inhibition of Rac.The low molecular mass GTPases of the Rho family (e.g., Rho, Rac, and Cdc42) are molecular switches in many cellular signaling cascades (Van Aelst and D'Souza-Schorey, 1997;Bishop and Hall, 2000). They are critically involved in the regulations of the actin cytoskeleton by extracellular signals (Kaibuchi et al., 1999) but function as switches also in various other signal processes (Nobes and Hall, 1995;Kjoller and Hall, 1999;Bokoch, 2000). Clostridial cytotoxins are established as pharmacological tools to study the function and the role of Rho GTPase proteins in signal transduction pathways. C3 transferases selectively ADP-ribosylate RhoA, RhoB, and RhoC, thereby inhibiting their biological functions (Aktories et al., 1989;Chardin et al., 1989;Paterson et al., 1990). The family of large clostridial cytotoxins inactivates small GTPases by glucosylation (Aktories and Just, 1995). Whereas Clostridium difficile toxins A and B inactivate all Rho GTPases, including Rho, Rac, and Cdc42 , the lethal toxin from Clostridium sordellii inactivates Rac, possibly Cdc42, but not Rho . In addition, Ras subfamily proteins (e.g., Ras, Ral, and Rap) are targets of the lethal toxin.Using the clostridial toxins as pharmacological tools, it was shown that exocytosis of RBL 2H3-hm1 cells induced by stimulation of the high-affinity antigen receptor Fc⑀RI involves Rho GTPases (Prepens et al., 1996). In Fc⑀RI signaling in RBL cells, Rac but not RhoA seems to be involved on various levels of the signal pathway, ultimately resulting in exocytosis. Rac is essential for Fc⑀RI-mediated calcium mobilization (Djouder et al., 2000). Rac participates in phospholipase C␥ activation (Hong-Geller et a...
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