{"id":{"repo_id":"uiuc","oai_identifier":"oai:www.ideals.illinois.edu:2142/70706"},"canonical_url":"https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/70706","repository":{"repo_id":"uiuc","name":"University of Illinois - Urbana-Champaign","base_url":"https://www.ideals.illinois.edu/oai-pmh"},"display":{"title":"Modeling and Ion Mapping of Intracellular Calcium Distribution in Molluscan Neural Somata","abstract":"To understand the mechanism of rapid (time constants of 1-3 sec) buffering of intracellular calcium in molluscan cell bodies, a diffusion-reaction model was developed. The model took into account the binding reactions of Ca('2+) with a calcium-indicating dye (arsenazo III) and an endogenous Ca('2+) buffer. The results from this model show that intracellular calcium can be buffered rapidly and dominantly by an endogenous buffer independent of mitochondrial Ca('2+) uptake and calcium pumps. During stimulation of the model cell, the submembrane calcium ion concentration can reach more than 1,000 times the steady-state value. Futhermore, Ca('2+) is restricted to within a few microns from the cell plasma membrane as it diffuses intracellularly. The accumulation of high concentration of Ca('2+) at the submembrane region can explain a number of properties of membrane calcium current I(,Ca) in molluscan neurons: (i) Decay kinetics of I(,Ca) during a voltage clamp depolarization period; (ii) I(,Ca)-Voltage relation; (iii) I(,Ca) as a function of intracellular calcium ion concentration; (iv) I(,Ca) as a function of extracellular calcium ion concentration. To understand the morphological bases of this model, I used electron microscopy and ion microscopy to probe the structure of the neurons in the mollusc Archidoris montereyensis. Electron microscopy showed that calcium-containing granules (lipochondria) exist in large numbers at the plasmalemma of these neurons. Ion images of the neurons processed by freeze-substitution showed that the nucleus consistently contains less calcium than the cytoplasm. These results suggest that in these neurons, the calcium buffering capacity of the cytoplasm is greater than that of the nucleus.","abstract_html":"To understand the mechanism of rapid (time constants of 1-3 sec) buffering of intracellular calcium in molluscan cell bodies, a diffusion-reaction model was developed. The model took into account the binding reactions of Ca('2+) with a calcium-indicating dye (arsenazo III) and an endogenous Ca('2+) buffer. The results from this model show that intracellular calcium can be buffered rapidly and dominantly by an endogenous buffer independent of mitochondrial Ca('2+) uptake and calcium pumps. During stimulation of the model cell, the submembrane calcium ion concentration can reach more than 1,000 times the steady-state value. Futhermore, Ca('2+) is restricted to within a few microns from the cell plasma membrane as it diffuses intracellularly. The accumulation of high concentration of Ca('2+) at the submembrane region can explain a number of properties of membrane calcium current I(,Ca) in molluscan neurons: (i) Decay kinetics of I(,Ca) during a voltage clamp depolarization period; (ii) I(,Ca)-Voltage relation; (iii) I(,Ca) as a function of intracellular calcium ion concentration; (iv) I(,Ca) as a function of extracellular calcium ion concentration. To understand the morphological bases of this model, I used electron microscopy and ion microscopy to probe the structure of the neurons in the mollusc Archidoris montereyensis. Electron microscopy showed that calcium-containing granules (lipochondria) exist in large numbers at the plasmalemma of these neurons. Ion images of the neurons processed by freeze-substitution showed that the nucleus consistently contains less calcium than the cytoplasm. These results suggest that in these neurons, the calcium buffering capacity of the cytoplasm is greater than that of the nucleus.","abstract_has_math":false,"creators":["Jung, Frank"],"institution":"University of Illinois at Urbana-Champaign","degree_name":"Ph.D.","degree_level":"Dissertation","degree_discipline":"Biophysics","degree_department":null,"school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2014,"date_issued":"2014-12-16T03:57:54Z","date_published":"2014-12-16T03:57:54Z","updated_at":"2026-07-22T22:26:03Z","subjects":["Biophysics, General"],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[{"key":"dc:identifier","label":"Identifier","values":["(UMI)AAI8309965"],"render_values":[{"text":"(UMI)AAI8309965","href":null,"code":true}]}]},"links":{"outbound_url":"http://hdl.handle.net/2142/70706","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:creator","label":"Author","values":["Jung, Frank"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2014-12-16T03:57:54Z","10000-01-01","1983"]},{"key":"dc:type","label":"Dc Type","values":["text"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Biophysics"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Dissertation"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Ph.D."]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["University of Illinois at Urbana-Champaign"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Biophysics, General"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["http://hdl.handle.net/2142/70706","(UMI)AAI8309965"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["To understand the mechanism of rapid (time constants of 1-3 sec) buffering of intracellular calcium in molluscan cell bodies, a diffusion-reaction model was developed. The model took into account the binding reactions of Ca('2+) with a calcium-indicating dye (arsenazo III) and an endogenous Ca('2+) buffer. The results from this model show that intracellular calcium can be buffered rapidly and dominantly by an endogenous buffer independent of mitochondrial Ca('2+) uptake and calcium pumps. During stimulation of the model cell, the submembrane calcium ion concentration can reach more than 1,000 times the steady-state value. Futhermore, Ca('2+) is restricted to within a few microns from the cell plasma membrane as it diffuses intracellularly. The accumulation of high concentration of Ca('2+) at the submembrane region can explain a number of properties of membrane calcium current I(,Ca) in molluscan neurons: (i) Decay kinetics of I(,Ca) during a voltage clamp depolarization period; (ii) I(,Ca)-Voltage relation; (iii) I(,Ca) as a function of intracellular calcium ion concentration; (iv) I(,Ca) as a function of extracellular calcium ion concentration. To understand the morphological bases of this model, I used electron microscopy and ion microscopy to probe the structure of the neurons in the mollusc Archidoris montereyensis. Electron microscopy showed that calcium-containing granules (lipochondria) exist in large numbers at the plasmalemma of these neurons. Ion images of the neurons processed by freeze-substitution showed that the nucleus consistently contains less calcium than the cytoplasm. These results suggest that in these neurons, the calcium buffering capacity of the cytoplasm is greater than that of the nucleus.","Made available in DSpace on 2014-12-16T03:57:54Z (GMT). No. of bitstreams: 1 8309965.pdf: 8186756 bytes, checksum: 605770d1515c9aedd96d9da9d0d43bf3 (MD5) Previous issue date: 1983","Embargo set by: Seth Robbins for item 70872 Lift date: Forever Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs","Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs","U of I Only","275 p.","Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1983."]},{"key":"dc:title","label":"Title","values":["Modeling and Ion Mapping of Intracellular Calcium Distribution in Molluscan Neural Somata"]}]}],"canonical_facts":{"dc:creator":["Jung, Frank"],"dc:date":["2014-12-16T03:57:54Z","10000-01-01","1983"],"dc:description":["To understand the mechanism of rapid (time constants of 1-3 sec) buffering of intracellular calcium in molluscan cell bodies, a diffusion-reaction model was developed. The model took into account the binding reactions of Ca('2+) with a calcium-indicating dye (arsenazo III) and an endogenous Ca('2+) buffer. The results from this model show that intracellular calcium can be buffered rapidly and dominantly by an endogenous buffer independent of mitochondrial Ca('2+) uptake and calcium pumps. During stimulation of the model cell, the submembrane calcium ion concentration can reach more than 1,000 times the steady-state value. Futhermore, Ca('2+) is restricted to within a few microns from the cell plasma membrane as it diffuses intracellularly. The accumulation of high concentration of Ca('2+) at the submembrane region can explain a number of properties of membrane calcium current I(,Ca) in molluscan neurons: (i) Decay kinetics of I(,Ca) during a voltage clamp depolarization period; (ii) I(,Ca)-Voltage relation; (iii) I(,Ca) as a function of intracellular calcium ion concentration; (iv) I(,Ca) as a function of extracellular calcium ion concentration. To understand the morphological bases of this model, I used electron microscopy and ion microscopy to probe the structure of the neurons in the mollusc Archidoris montereyensis. Electron microscopy showed that calcium-containing granules (lipochondria) exist in large numbers at the plasmalemma of these neurons. Ion images of the neurons processed by freeze-substitution showed that the nucleus consistently contains less calcium than the cytoplasm. These results suggest that in these neurons, the calcium buffering capacity of the cytoplasm is greater than that of the nucleus.","Made available in DSpace on 2014-12-16T03:57:54Z (GMT). No. of bitstreams: 1 8309965.pdf: 8186756 bytes, checksum: 605770d1515c9aedd96d9da9d0d43bf3 (MD5) Previous issue date: 1983","Embargo set by: Seth Robbins for item 70872 Lift date: Forever Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs","Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs","U of I Only","275 p.","Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1983."],"dc:identifier":["http://hdl.handle.net/2142/70706","(UMI)AAI8309965"],"dc:subject":["Biophysics, General"],"dc:title":["Modeling and Ion Mapping of Intracellular Calcium Distribution in Molluscan Neural Somata"],"dc:type":["text"],"thesis:degree_discipline":["Biophysics"],"thesis:degree_level":["Dissertation"],"thesis:degree_name":["Ph.D."],"thesis:institution_name":["University of Illinois at Urbana-Champaign"]},"updated_at":"2026-07-22T22:26:03Z"}