Capacitance Measurements of Exocytosis From AII Amacrine Cells in Retinal Slices
During neuronal synaptic transmission, the exocytotic release of neurotransmitters from synaptic vesicles in the presynaptic neuron evokes a change in conductance for one or more types of ligand-gated ion channels in the postsynaptic neuron. The standard method of investigation uses electrophysiolog...
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Bio-protocol LLC
2025-01-01
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| author | Espen Hartveit Margaret Veruki |
| author_facet | Espen Hartveit Margaret Veruki |
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| description | During neuronal synaptic transmission, the exocytotic release of neurotransmitters from synaptic vesicles in the presynaptic neuron evokes a change in conductance for one or more types of ligand-gated ion channels in the postsynaptic neuron. The standard method of investigation uses electrophysiological recordings of the postsynaptic response. However, electrophysiological recordings can directly quantify the presynaptic release of neurotransmitters with high temporal resolution by measuring the membrane capacitance before and after exocytosis, as fusion of the membrane of presynaptic vesicles with the plasma membrane increases the total capacitance. While the standard technique for capacitance measurement assumes that the presynaptic cell is unbranched and can be represented as a simple resistance-capacitance (RC) circuit, neuronal exocytosis typically occurs at a distance from the soma. Even in such cases, however, it can be possible to detect a depolarization-evoked increase in capacitance. Here, we provide a detailed, step-by-step protocol that describes how "Sine + DC" (direct current) capacitance measurements can quantify the exocytotic release of neurotransmitters from AII amacrine cells in rat retinal slices. The AII is an important inhibitory interneuron of the mammalian retina that plays an important role in integrating rod and cone pathway signals. AII amacrines release glycine from their presynaptic dendrites, and capacitance measurements have been important for understanding the release properties of these dendrites. When the goal is to directly quantify the presynaptic release, there is currently no other competing method available. This protocol includes procedures for measuring depolarization-evoked exocytosis, using both standard square-wave pulses, arbitrary stimulus waveforms, and synaptic input. |
| format | Article |
| id | doaj-art-033358e546e14d0fa3bb41380a55fe27 |
| institution | Kabale University |
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| language | English |
| publishDate | 2025-01-01 |
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| spelling | doaj-art-033358e546e14d0fa3bb41380a55fe272025-02-07T08:16:31ZengBio-protocol LLCBio-Protocol2331-83252025-01-0115110.21769/BioProtoc.5147Capacitance Measurements of Exocytosis From AII Amacrine Cells in Retinal SlicesEspen Hartveit0Margaret Veruki1Department of Biomedicine, University of Bergen, Bergen, NorwayMohn Research Center for the Brain, Bergen, NorwayDepartment of Biomedicine, University of Bergen, Bergen, NorwayMohn Research Center for the Brain, Bergen, NorwayDuring neuronal synaptic transmission, the exocytotic release of neurotransmitters from synaptic vesicles in the presynaptic neuron evokes a change in conductance for one or more types of ligand-gated ion channels in the postsynaptic neuron. The standard method of investigation uses electrophysiological recordings of the postsynaptic response. However, electrophysiological recordings can directly quantify the presynaptic release of neurotransmitters with high temporal resolution by measuring the membrane capacitance before and after exocytosis, as fusion of the membrane of presynaptic vesicles with the plasma membrane increases the total capacitance. While the standard technique for capacitance measurement assumes that the presynaptic cell is unbranched and can be represented as a simple resistance-capacitance (RC) circuit, neuronal exocytosis typically occurs at a distance from the soma. Even in such cases, however, it can be possible to detect a depolarization-evoked increase in capacitance. Here, we provide a detailed, step-by-step protocol that describes how "Sine + DC" (direct current) capacitance measurements can quantify the exocytotic release of neurotransmitters from AII amacrine cells in rat retinal slices. The AII is an important inhibitory interneuron of the mammalian retina that plays an important role in integrating rod and cone pathway signals. AII amacrines release glycine from their presynaptic dendrites, and capacitance measurements have been important for understanding the release properties of these dendrites. When the goal is to directly quantify the presynaptic release, there is currently no other competing method available. This protocol includes procedures for measuring depolarization-evoked exocytosis, using both standard square-wave pulses, arbitrary stimulus waveforms, and synaptic input.https://bio-protocol.org/en/bpdetail?id=5147&type=0 |
| spellingShingle | Espen Hartveit Margaret Veruki Capacitance Measurements of Exocytosis From AII Amacrine Cells in Retinal Slices Bio-Protocol |
| title | Capacitance Measurements of Exocytosis From AII Amacrine Cells in Retinal Slices |
| title_full | Capacitance Measurements of Exocytosis From AII Amacrine Cells in Retinal Slices |
| title_fullStr | Capacitance Measurements of Exocytosis From AII Amacrine Cells in Retinal Slices |
| title_full_unstemmed | Capacitance Measurements of Exocytosis From AII Amacrine Cells in Retinal Slices |
| title_short | Capacitance Measurements of Exocytosis From AII Amacrine Cells in Retinal Slices |
| title_sort | capacitance measurements of exocytosis from aii amacrine cells in retinal slices |
| url | https://bio-protocol.org/en/bpdetail?id=5147&type=0 |
| work_keys_str_mv | AT espenhartveit capacitancemeasurementsofexocytosisfromaiiamacrinecellsinretinalslices AT margaretveruki capacitancemeasurementsofexocytosisfromaiiamacrinecellsinretinalslices |