5) (Kaether et al., 2000; MacAskill & Kittler, 2010). For time-lapse

imaging with electrical field stimulation, neurons in Tyrode’s solution (119 mm NaCl, 2.5 mm KCl, 2 mm CaCl2, 2 mm MgCl2, CP-868596 price 25 mm HEPES and 30 mm glucose, pH 7.4) with 10 μm 6-cyano-7-nitroquinoxaline-2,3-dione (Tocris, Ellisville, MO, USA) and 50 μm D(-)-2-amino-5-phosphonovaleric acid (Tocris) or in low-Ca2+ Tyrode’s solution (119 mm NaCl, 2.5 mm KCl, 0.1 mm CaCl2, 4 mm MgCl2, 25 mm HEPES and 30 mm glucose, pH 7.4) with 10 μm 6-cyano-7-nitroquinoxaline-2,3-dione and 50 μm D(-)-2-amino-5-phosphonovaleric acid were placed on a heated stage (set at 37 °C) with a home-prepared acrylic box to prevent temperature fluctuation. Electrical field stimulation (1 ms duration, 400 stimuli,

40 Hz) was applied by two parallel platinum wires (between wires approximately 6 mm and approximately 1 mm distance from cells; Sigma-Aldrich, Tokyo, Japan) that were mounted in a plastic lid (Gärtner & Staiger, 2002). The mCherry-OMP dynamics were imaged at intervals of 3 s for 50 min with 3 min interval electrical stimulation of 40 Hz for 10 s. After time-lapse imaging, changes of G-CaMP6 fluorescence intensity elucidated by the same electrical stimulation were measured at approximately 3 Hz at the same axonal region. For time-lapse imaging in low-Ca2+ Tyrode’s solution, the G-CaMP6 measurements were performed both before and after replacing the Tyrode’s solution with normal Ca2+ concentration. We set the excitation laser power Ganetespib to be minimal but sufficient to obtain images with enough dynamic range. During imaging periods, reduction of mitochondrial mobility and impairment of mitochondrial morphology or distribution were not observed (De Vos & Sheetz, 2007).

We classified the axonal mitochondria into two dynamic states, stationary and mobile (Fig. 1A). We defined mitochondria that remained for ≧ 30 min at the same axonal region as stationary states (SS), and others as mobile states. Mobile mitochondria showed saltatory movement, science including moving periods (M) and short pauses (SP) (temporary stops). The definition of a short pause is given in the following section. Image analysis and quantification were performed by using ImageJ (NIH, Bethesda, MD, USA) and custom-written software (Visual Studio; Microsoft, Seattle, WA, USA). For all images, the average background pixel intensity of the individual image was subtracted before image processing. In mCherry-OMP, EGFP-VAMP2, FM1-43(Δ) and APP-mCherry images, puncta were identified as local fluorescence increases, which were > 0.15 μm2 and three times higher fluorescence intensities than the background fluorescence of nearby axonal regions without obvious fluorescence clusters.