Presynaptic target of Ca2+ action on neuropeptide and acetylcholine release in Aplysia californica
When buccal neuron B2 of Aplysia californica is co-cultured with sensory neurons (SNs), slow peptidergic synapses are formed. When B2 is co-cultured with neurons B3 or B6, fast cholinergic synapses are formed. Patch pipettes were used to voltage clamp pre- and postsynaptic neurons and to load the ca...
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description | When buccal neuron B2 of Aplysia californica is co-cultured with sensory neurons (SNs), slow peptidergic synapses are formed. When B2 is co-cultured with neurons B3 or
B6, fast cholinergic synapses are formed.
Patch pipettes were used to voltage clamp pre- and postsynaptic neurons and to load the caged Ca 2+ chelator o -nitrophenyl EGTA (NPE) and the Ca 2+ indicator BTC into presynaptic neurons. The relationships between presynaptic [Ca 2+ ] i and postsynaptic responses were compared between peptidergic and cholinergic synapses formed by cell B2.
Using variable intensity flashes, Ca 2+ stoichiometries of peptide and acetylcholine (ACh) release were approximately 2 and 3, respectively. The difference did not
reach statistical significance.
ACh quanta summate linearly postsynaptically. We also found a linear dose-response curve for peptide action, indicating a
linear relationship between submaximal peptide concentration and response of the SN.
The minimum intracellular calcium concentrations ([Ca 2+ ] i ) for triggering peptidergic and cholinergic transmission were estimated to be about 5 and 10 μ m , respectively.
By comparing normal postsynaptic responses to those evoked by photolysis of NPE, we estimate [Ca 2+ ] i at the release trigger site elicited by a single action potential (AP) to be at least 10 μ m for peptidergic synapses and probably higher for cholinergic synapses.
Cholinergic release is brief (half-width â200 ms), even in response to a prolonged rise in [Ca 2+ ] i , while some peptidergic release appears to persist for as long as [Ca 2+ ] i remains elevated (for up to 10 s). This may reflect differences in sizes of reserve pools, or in replenishment rates of immediately
releasable pools of vesicles.
Electron microscopy revealed that most synaptic contacts had at least one morphologically docked dense core vesicle that presumably
contained peptide; these were often located within conventional active zones.
Both cholinergic and peptidergic vesicles are docked within active zones, but cholinergic vesicles may be located closer to
Ca 2+ channels than are peptidergic vesicles. |
doi_str_mv | 10.1111/j.1469-7793.2001.00647.x |
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B6, fast cholinergic synapses are formed.
Patch pipettes were used to voltage clamp pre- and postsynaptic neurons and to load the caged Ca 2+ chelator o -nitrophenyl EGTA (NPE) and the Ca 2+ indicator BTC into presynaptic neurons. The relationships between presynaptic [Ca 2+ ] i and postsynaptic responses were compared between peptidergic and cholinergic synapses formed by cell B2.
Using variable intensity flashes, Ca 2+ stoichiometries of peptide and acetylcholine (ACh) release were approximately 2 and 3, respectively. The difference did not
reach statistical significance.
ACh quanta summate linearly postsynaptically. We also found a linear dose-response curve for peptide action, indicating a
linear relationship between submaximal peptide concentration and response of the SN.
The minimum intracellular calcium concentrations ([Ca 2+ ] i ) for triggering peptidergic and cholinergic transmission were estimated to be about 5 and 10 μ m , respectively.
By comparing normal postsynaptic responses to those evoked by photolysis of NPE, we estimate [Ca 2+ ] i at the release trigger site elicited by a single action potential (AP) to be at least 10 μ m for peptidergic synapses and probably higher for cholinergic synapses.
Cholinergic release is brief (half-width â200 ms), even in response to a prolonged rise in [Ca 2+ ] i , while some peptidergic release appears to persist for as long as [Ca 2+ ] i remains elevated (for up to 10 s). This may reflect differences in sizes of reserve pools, or in replenishment rates of immediately
releasable pools of vesicles.
Electron microscopy revealed that most synaptic contacts had at least one morphologically docked dense core vesicle that presumably
contained peptide; these were often located within conventional active zones.
Both cholinergic and peptidergic vesicles are docked within active zones, but cholinergic vesicles may be located closer to
Ca 2+ channels than are peptidergic vesicles.</description><identifier>ISSN: 0022-3751</identifier><identifier>EISSN: 1469-7793</identifier><identifier>DOI: 10.1111/j.1469-7793.2001.00647.x</identifier><identifier>PMID: 11559764</identifier><language>eng</language><publisher>Oxford, UK: The Physiological Society</publisher><subject>Acetylcholine - metabolism ; Action Potentials - drug effects ; Algorithms ; Animals ; Aplysia ; Calcium - physiology ; Calibration ; Cells, Cultured ; Chelating Agents - pharmacology ; Dose-Response Relationship, Drug ; In Vitro Techniques ; Microscopy, Electron ; Neurons - metabolism ; Neurons - ultrastructure ; Neuropeptides - metabolism ; Original ; Patch-Clamp Techniques ; Receptors, Presynaptic - metabolism ; Receptors, Presynaptic - ultrastructure ; Synaptic Transmission ; Ultraviolet Rays</subject><ispartof>The Journal of physiology, 2001-09, Vol.535 (3), p.647-662</ispartof><rights>2001 The Journal of Physiology © 2001 The Physiological Society</rights><rights>The Physiological Society 2001 2001</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2278817/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2278817/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,1411,1427,27901,27902,45550,45551,46384,46808,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11559764$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ohnuma, Kiyoshi</creatorcontrib><creatorcontrib>Whim, Matthew D.</creatorcontrib><creatorcontrib>Fetter, Richard D.</creatorcontrib><creatorcontrib>Kaczmarek, Leonard K.</creatorcontrib><creatorcontrib>Zucker, Robert S.</creatorcontrib><title>Presynaptic target of Ca2+ action on neuropeptide and acetylcholine release in Aplysia californica</title><title>The Journal of physiology</title><addtitle>J Physiol</addtitle><description>When buccal neuron B2 of Aplysia californica is co-cultured with sensory neurons (SNs), slow peptidergic synapses are formed. When B2 is co-cultured with neurons B3 or
B6, fast cholinergic synapses are formed.
Patch pipettes were used to voltage clamp pre- and postsynaptic neurons and to load the caged Ca 2+ chelator o -nitrophenyl EGTA (NPE) and the Ca 2+ indicator BTC into presynaptic neurons. The relationships between presynaptic [Ca 2+ ] i and postsynaptic responses were compared between peptidergic and cholinergic synapses formed by cell B2.
Using variable intensity flashes, Ca 2+ stoichiometries of peptide and acetylcholine (ACh) release were approximately 2 and 3, respectively. The difference did not
reach statistical significance.
ACh quanta summate linearly postsynaptically. We also found a linear dose-response curve for peptide action, indicating a
linear relationship between submaximal peptide concentration and response of the SN.
The minimum intracellular calcium concentrations ([Ca 2+ ] i ) for triggering peptidergic and cholinergic transmission were estimated to be about 5 and 10 μ m , respectively.
By comparing normal postsynaptic responses to those evoked by photolysis of NPE, we estimate [Ca 2+ ] i at the release trigger site elicited by a single action potential (AP) to be at least 10 μ m for peptidergic synapses and probably higher for cholinergic synapses.
Cholinergic release is brief (half-width â200 ms), even in response to a prolonged rise in [Ca 2+ ] i , while some peptidergic release appears to persist for as long as [Ca 2+ ] i remains elevated (for up to 10 s). This may reflect differences in sizes of reserve pools, or in replenishment rates of immediately
releasable pools of vesicles.
Electron microscopy revealed that most synaptic contacts had at least one morphologically docked dense core vesicle that presumably
contained peptide; these were often located within conventional active zones.
Both cholinergic and peptidergic vesicles are docked within active zones, but cholinergic vesicles may be located closer to
Ca 2+ channels than are peptidergic vesicles.</description><subject>Acetylcholine - metabolism</subject><subject>Action Potentials - drug effects</subject><subject>Algorithms</subject><subject>Animals</subject><subject>Aplysia</subject><subject>Calcium - physiology</subject><subject>Calibration</subject><subject>Cells, Cultured</subject><subject>Chelating Agents - pharmacology</subject><subject>Dose-Response Relationship, Drug</subject><subject>In Vitro Techniques</subject><subject>Microscopy, Electron</subject><subject>Neurons - metabolism</subject><subject>Neurons - ultrastructure</subject><subject>Neuropeptides - metabolism</subject><subject>Original</subject><subject>Patch-Clamp Techniques</subject><subject>Receptors, Presynaptic - metabolism</subject><subject>Receptors, Presynaptic - ultrastructure</subject><subject>Synaptic Transmission</subject><subject>Ultraviolet Rays</subject><issn>0022-3751</issn><issn>1469-7793</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkV2L1DAUhoMo7uzqX5Bc6YW05qNpWhBhGVw_WHAv1uuQpqfTDJmkJh13--9NnXXVEMiB9znvIedFCFNS0nze7Uta1W0hZctLRggtCakrWd4_QZtH4SnaEMJYwaWgZ-g8pX0GOWnb5-iMUiFaWVcb1N1ESIvX02wNnnXcwYzDgLeavcXazDZ4nK-HYwwTZKgHrH2fJZgXZ8bgrAccwYFOgK3Hl5NbktXYaGeHEL01-gV6NmiX4OXDe4G-X3283X4urr99-rK9vC5GzlpZNK1pKsI4JRXjPW-ZINpw2ddCDK2mhpgBWKPzd_pB1My0mnVV19GqIQDaGH6BPpx8p2N3gN6An6N2aor2oOOigrbqf8XbUe3CT8WYbBoqs8HrB4MYfhwhzepgkwHntIdwTEpSKgWpSAZf_TvpccSftWbg_Qm4sw6WvzpRa3xqr9aU1JqSWuNTv-NT9-r2600ucvubU_tod-OdjaCmMW81pGBs3rsSXCiuVvIXWF6dqA</recordid><startdate>20010915</startdate><enddate>20010915</enddate><creator>Ohnuma, Kiyoshi</creator><creator>Whim, Matthew D.</creator><creator>Fetter, Richard D.</creator><creator>Kaczmarek, Leonard K.</creator><creator>Zucker, Robert S.</creator><general>The Physiological Society</general><general>Blackwell Science Ltd</general><general>Blackwell Science Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20010915</creationdate><title>Presynaptic target of Ca2+ action on neuropeptide and acetylcholine release in Aplysia californica</title><author>Ohnuma, Kiyoshi ; Whim, Matthew D. ; Fetter, Richard D. ; Kaczmarek, Leonard K. ; Zucker, Robert S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h3297-89c8402310423d39250ac37d655f9a1c0cfe28a375df562c9a2b4bb1480eeacc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Acetylcholine - metabolism</topic><topic>Action Potentials - drug effects</topic><topic>Algorithms</topic><topic>Animals</topic><topic>Aplysia</topic><topic>Calcium - physiology</topic><topic>Calibration</topic><topic>Cells, Cultured</topic><topic>Chelating Agents - pharmacology</topic><topic>Dose-Response Relationship, Drug</topic><topic>In Vitro Techniques</topic><topic>Microscopy, Electron</topic><topic>Neurons - metabolism</topic><topic>Neurons - ultrastructure</topic><topic>Neuropeptides - metabolism</topic><topic>Original</topic><topic>Patch-Clamp Techniques</topic><topic>Receptors, Presynaptic - metabolism</topic><topic>Receptors, Presynaptic - ultrastructure</topic><topic>Synaptic Transmission</topic><topic>Ultraviolet Rays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ohnuma, Kiyoshi</creatorcontrib><creatorcontrib>Whim, Matthew D.</creatorcontrib><creatorcontrib>Fetter, Richard D.</creatorcontrib><creatorcontrib>Kaczmarek, Leonard K.</creatorcontrib><creatorcontrib>Zucker, Robert S.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ohnuma, Kiyoshi</au><au>Whim, Matthew D.</au><au>Fetter, Richard D.</au><au>Kaczmarek, Leonard K.</au><au>Zucker, Robert S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Presynaptic target of Ca2+ action on neuropeptide and acetylcholine release in Aplysia californica</atitle><jtitle>The Journal of physiology</jtitle><addtitle>J Physiol</addtitle><date>2001-09-15</date><risdate>2001</risdate><volume>535</volume><issue>3</issue><spage>647</spage><epage>662</epage><pages>647-662</pages><issn>0022-3751</issn><eissn>1469-7793</eissn><abstract>When buccal neuron B2 of Aplysia californica is co-cultured with sensory neurons (SNs), slow peptidergic synapses are formed. When B2 is co-cultured with neurons B3 or
B6, fast cholinergic synapses are formed.
Patch pipettes were used to voltage clamp pre- and postsynaptic neurons and to load the caged Ca 2+ chelator o -nitrophenyl EGTA (NPE) and the Ca 2+ indicator BTC into presynaptic neurons. The relationships between presynaptic [Ca 2+ ] i and postsynaptic responses were compared between peptidergic and cholinergic synapses formed by cell B2.
Using variable intensity flashes, Ca 2+ stoichiometries of peptide and acetylcholine (ACh) release were approximately 2 and 3, respectively. The difference did not
reach statistical significance.
ACh quanta summate linearly postsynaptically. We also found a linear dose-response curve for peptide action, indicating a
linear relationship between submaximal peptide concentration and response of the SN.
The minimum intracellular calcium concentrations ([Ca 2+ ] i ) for triggering peptidergic and cholinergic transmission were estimated to be about 5 and 10 μ m , respectively.
By comparing normal postsynaptic responses to those evoked by photolysis of NPE, we estimate [Ca 2+ ] i at the release trigger site elicited by a single action potential (AP) to be at least 10 μ m for peptidergic synapses and probably higher for cholinergic synapses.
Cholinergic release is brief (half-width â200 ms), even in response to a prolonged rise in [Ca 2+ ] i , while some peptidergic release appears to persist for as long as [Ca 2+ ] i remains elevated (for up to 10 s). This may reflect differences in sizes of reserve pools, or in replenishment rates of immediately
releasable pools of vesicles.
Electron microscopy revealed that most synaptic contacts had at least one morphologically docked dense core vesicle that presumably
contained peptide; these were often located within conventional active zones.
Both cholinergic and peptidergic vesicles are docked within active zones, but cholinergic vesicles may be located closer to
Ca 2+ channels than are peptidergic vesicles.</abstract><cop>Oxford, UK</cop><pub>The Physiological Society</pub><pmid>11559764</pmid><doi>10.1111/j.1469-7793.2001.00647.x</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acetylcholine - metabolism Action Potentials - drug effects Algorithms Animals Aplysia Calcium - physiology Calibration Cells, Cultured Chelating Agents - pharmacology Dose-Response Relationship, Drug In Vitro Techniques Microscopy, Electron Neurons - metabolism Neurons - ultrastructure Neuropeptides - metabolism Original Patch-Clamp Techniques Receptors, Presynaptic - metabolism Receptors, Presynaptic - ultrastructure Synaptic Transmission Ultraviolet Rays |
title | Presynaptic target of Ca2+ action on neuropeptide and acetylcholine release in Aplysia californica |
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