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Image Search Results
Journal: Proceedings of the National Academy of Sciences of the United States of America
Article Title: Synaptic crosstalk conferred by a zone of differentially regulated Ca 2+ signaling in the dendritic shaft adjoining a potentiated spine
doi: 10.1073/pnas.1902461116
Figure Lengend Snippet: LTCC activity level governs the spread along the dendritic shaft of STIM1 feedback inhibition of dendritic LTCCs. (A) Mean total cytosolic Ca2+ (RGECO1) changes by uncaging on 79wt neurons at 0 μm. Mean (black) ± SEM (dark gray). Uncaging occurred from 0 to 60 s, at 1 Hz. (B) Mean LTCC-independent Ca2+ changes (IF) in the cytosol by uncaging at 0 μm in the same neurons as A and pretreated with nimodipine (5 μM) for 15 min. Mean (black) ± SEM (red). (C) Mean LTCC-dependent Ca2+ changes (DF) at 0 μm, calculated by subtracting the non-LTCC Ca2+ time course from the total Ca2+ time course of the same neuron. Mean (black) ± SEM (blue). (D) Mean integrated increase in total cytosolic Ca2+ (shaded gray region in A) along a dendrite of 79wt (circles; n = 5), 79ΔPIX (squares; n = 5), and 79ΔPKA (diamonds; n = 6) neurons. Mean ± SEM. (E) Mean integrated increase in the LTCC-independent component of cytosolic Ca2+ (IF; shaded pink region in B) along a dendrite of 79wt (circles; n = 5), 79ΔPIX (squares; n = 5), and 79ΔPKA (diamonds; n = 6) neurons. Mean ± SEM. (F) Mean integrated increase in LTCC-dependent component of cytosolic Ca2+ (DF; shaded light blue region in C) along a dendrite of 79wt (circles; n = 5), 79ΔPIX (squares; n = 5), and 79ΔPKA (diamonds; n = 6) neurons. Mean ± SEM.
Article Snippet: D1ER (Addgene no. 36325),
Techniques: Activity Assay, Inhibition
Journal: Proceedings of the National Academy of Sciences of the United States of America
Article Title: Synaptic crosstalk conferred by a zone of differentially regulated Ca 2+ signaling in the dendritic shaft adjoining a potentiated spine
doi: 10.1073/pnas.1902461116
Figure Lengend Snippet: β-adrenergic receptors modulate a zone of Ca2+ signaling in the dendritic shaft adjoining a potentiated spine. (A) In neurons treated with Iso, time course of change in total cytosolic Ca2+ (IF + DF, imaged with RGECO1) (n = 5) measured at 0 μm from the uncaging-stimulated spine. Mean (black) ± SEM (dark gray). (B) After 15 min nimodipine treatment, time course of change in LTCC-independent cytosolic Ca2+ (IF) of the neurons in A, measured at 0 μm. Mean (black) ± SEM (red). (C) Time course of increase in LTCC-dependent cytosolic Ca2+ (DF) (DF = total – IF) at 0 μm. Mean (black) ± SEM (blue). (D) Spatial profile for integrated increase in total cytosolic Ca2+ (IF + DF) shaded gray region in A along the dendrite of Iso-treated (1 μM; open circles; n = 5) versus untreated (control) neurons (shaded circles; n = 5) and for Iso-treated + STIM1 knockdown (squares; n = 5). Mean ± SEM. (E) Spatial profile for integrated increase in the LTCC-independent Ca2+ (IF; shaded pink region in B) along the dendrite of Iso-treated (open circles; n = 5) versus untreated (control) neurons (red circles; n = 5) and for Iso-treated + STIM1 knockdown (squares; n = 5). Mean ± SEM. (F) Spatial profile for average integrated increase in LTCC-dependent Ca2+ (DF; shaded light blue region in C) along the dendrite of Iso-treated (open circles; n = 5) versus untreated (control) neurons (blue circles; n = 5) and for Iso-treated + STIM1 knockdown (squares; n = 5). Mean ± SEM.
Article Snippet: D1ER (Addgene no. 36325),
Techniques: Control, Knockdown