2 μg/mL, CNIH-2; 1:50, pan-Type I TARP) in D-PBS plus 2% normal goat serum. Cultures were rinsed and incubated with fluorescence-conjugated secondary antibodies (Invitrogen, 1:500) in D-PBS for 1 hr at room temperature. After a final rinse, coverslips were mounted and imaged using Leica immunofluorescence

microscope systems (Wetzlar, Germany). Rat hippocampal slices (400 μm) were incubated in slicing buffer (in mM: 124 NaCl, 26 mM NaHCO3, 3 KCl, 10 Glucose, 0.5 CaCl2, and 4 MgCl2) for 1 hr. Slices were then placed into biotinylation solution (biotinylation solution = slicing solution except [CaCl2] and [MgCl2] were raised to 2.3 and 1.3 mM, respectively) ∼4°C biotinylation solution for 5 min. Surface proteins of the dissected

were labeled with sulfo NHS ATM/ATR cancer Sirolimus purchase SS biotin (1.5 mg/mL; Pierce) for 30 min on ice and the reaction quenched with glycine (50 mM). Hippocampi were homogenized with Tris buffer (TB: 50 mM Tris, pH 7.4, 2 mM EGTA) then sonicated. Homogenates were centrifuged at 100,000 × g for 20 min and the pellet was resuspended in TB containing NaCl (TN: TB + 100 mM NaCl). 50% ULTRA link Neutravidin (Roche) was added and incubated at 4°C for 2 hr. Nonbound internal protein solution was removed. Beads were washed with RIPA buffer and biotinylated surface proteins were eluted by boiling for 5 min in Laemmli buffer containing DTT (7.7 mg/mL). Eluted proteins and internal proteins were separated by SDS-PAGE and detected via western blotting. Data are represented as mean ± SEM and are the result of at least three independent experiments. Analyses involving three or more data sets were performed with a one-way ANOVA with a Tukey-Kramer post-hoc

analysis using GraphPad Prism software (Carlsbad, CA). Analyses involving two data sets were performed with an uncorrected Student’s t test or with a Student’s t test with a Welsh correction, only if the variances were statistically different. Significance was set as a p-value of less than 0.05. A.S.K., M.B.G., H.Y., Y.T., E.R.S., H.W., Y.-W.Q., E.S.N., and D.S.B. are full-time Idoxuridine employees of Eli Lilly and Company. This work was supported in part by grants to S.T. from the NIMH (R01MH077939) and the NINDS (RC1NS068966). “
“Neuronal somata and dendrites acidify when depolarized by trains of action potentials and voltage-clamp pulses (Ahmed and Connor, 1980, Trapp et al., 1996a, Trapp et al., 1996b and Willoughby and Schwiening, 2002), elevated extracellular [K+] (OuYang et al., 1995, Zhan et al., 1998 and Yu et al., 2003), or glutamate agonists (Vale-González et al., 2006 and Bolshakov et al., 2008). Most studies suggest that this depolarization-induced cytosolic acidification results from Ca2+ influx-mediated activation of the plasmalemmal Ca2+ ATPase, which imports H+ as it extrudes Ca2+ (Schwiening and Thomas, 1998 and Chesler, 2003).