Journal: Bio-protocol
Article Title: Capacitance Measurements of Exocytosis From AII Amacrine Cells in Retinal Slices
doi: 10.21769/BioProtoc.5147
Figure Lengend Snippet: A. Video micrograph of retinal slice visualized with IR-DGC microscopy. Note the cell body and thick apical dendrite of an AII amacrine cell (indicated by arrow), with the cell body in the inner nuclear layer (top) and the apical dendrite descending into the inner plexiform layer (bottom). Retinal layers are indicated by abbreviations (INL, inner nuclear layer; IPL, inner plexiform layer; GCL, ganglion cell layer). Scale bar (A, B): 10 μm. B. Same as in A, after establishing a whole-cell recording with a patch pipette positioned on the cell body of the AII (right). C. AII amacrine filled with Alexa 594 during whole-cell recording (different from A, B). Maximum intensity projection generated from widefield fluorescence image stack after deconvolution. Scale bar: 10 μm. D. Characteristic action currents (escape from voltage clamp) evoked in an AII amacrine during whole-cell recording in response to 5 ms depolarizing voltage pulses from V hold = -60 to -55 mV (voltage stimulus at top). Traces show responses recorded immediately after breaking into the cell (middle) and approximately 3 min later, after diffusion of QX314 from the intracellular pipette solution and block of voltage-gated Na + (Na v ) channels (bottom; n = 4 responses in each condition).
Article Snippet: N-(2,6-Dimethylphenylcarbamoylmethyl)triethylammonium chloride (QX314 chloride) (Tocris, catalog number: 2313, CAS number: 5369-03-9) 27.
Techniques: Microscopy, Transferring, Generated, Fluorescence, Diffusion-based Assay, Blocking Assay