Location: semantic-annotation @ 848b6a8fb585 / semgen_annotated_models / bindschadler_2001.cellml

Author:
Dewan Sarwar <sarwarcse@gmail.com>
Date:
2019-01-31 16:34:20+13:00
Desc:
Testing with Max's suggested way of annotation for weinstein_1995_max model
Permanent Source URI:
https://models.physiomeproject.org/workspace/584/rawfile/848b6a8fb585337adc4f3805c0ed682a6a5fd379/semgen_annotated_models/bindschadler_2001.cellml

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  <documentation xmlns="http://cellml.org/tmp-documentation">
    <article>
      <articleinfo>
        <title>A Bifurcation Analysis of Two Coupled Calcium Oscillators</title>
        <author>
          <firstname>Catherine</firstname>
          <surname>Lloyd</surname>
          <affiliation>
            <shortaffil>Auckland Bioengineering Institute, The University of Auckland</shortaffil>
          </affiliation>
        </author>
      </articleinfo>
      <section id="sec_status">
        <title>Model Status</title>
        <para>This CellML model runs in both OpenCell and COR to produce an oscillating output similar to that from the original published model. The units have been checked and they are consistent.</para>
      </section>
      <sect1 id="sec_structure">
        <title>Model Structure</title>
        <para>ABSTRACT: In many cell types, asynchronous or synchronous oscillations in the concentration of intracellular free calcium occur in adjacent cells that are coupled by gap junctions. Such oscillations are believed to underlie oscillatory intercellular calcium waves in some cell types, and thus it is important to understand how they occur and are modified by intercellular coupling. Using a previous model of intracellular calcium oscillations in pancreatic acinar cells, this article explores the effects of coupling two cells with a simple linear diffusion term. Depending on the concentration of a signal molecule, inositol (1,4,5)-trisphosphate, coupling two identical cells by diffusion can give rise to synchronized in-phase oscillations, as well as different-amplitude in-phase oscillations and same-amplitude antiphase oscillations. Coupling two nonidentical cells leads to more complex behaviors such as cascades of period doubling and multiply periodic solutions. This study is a first step towards understanding the role and significance of the diffusion of calcium through gap junctions in the coordination of oscillatory calcium waves in a variety of cell types.</para>
        <para>The original paper reference is cited below:</para>
        <para>
          A bifurcation analysis of two coupled calcium oscillators, Michael Bindschadler and James Sneyd, 2001,
          <emphasis>CHAOS</emphasis>
          , 11, 237-246.
          <ulink url="http://www.ncbi.nlm.nih.gov/pubmed/12779457">PubMed ID: 12779457</ulink>
        </para>
        <informalfigure float="0" id="fig_cell_diagram">
          <mediaobject>
            <imageobject>
              <objectinfo>
                <title>cell diagram</title>
              </objectinfo>
              <imagedata fileref="bindschadler_2001.png" />
            </imageobject>
            <caption>Schematic diagram of the IP3 receptor model.  The receptor with its three possible states: X, Y, and Z; representing open, shut and inactive respectively, is embedded within a model of intracellular calcium dynamics.</caption>
          </mediaobject>
        </informalfigure>
      </sect1>
    </article>
  </documentation>
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      <dcterms:description>Intercellular coupling permeability rate constant.</dcterms:description>
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      <dcterms:description>Constant for rate equation represented by phi 3</dcterms:description>
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      <dcterms:description>Constant for rate equation represented by phi 2</dcterms:description>
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      <dcterms:description>Constant for calculation of Ca flow via ATPase pumps</dcterms:description>
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              <semsim:name>Ca out of cell 2 cytoplasm to extracellular matrix via ATPase pumps</semsim:name>
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      <dcterms:description>Constant for rate equation represented by phi 3</dcterms:description>
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      <dcterms:description>Rate of change in IP3 receptors from the inactive state to open state in cell 2</dcterms:description>
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    <rdf:Description rdf:about="#h2.phi3_c2">
      <dcterms:description>Rate of change in IP3 receptors from the inactive state to open state in cell 2</dcterms:description>
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      <dcterms:description>Constant for rate equation represented by phi 3</dcterms:description>
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      <dcterms:description>Constant for rate equation represented by phi 3</dcterms:description>
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      <dcterms:description>Constant for rate equation represented by phi 2</dcterms:description>
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      <dcterms:description>Cell 1 Ca concentration in the cytoplasm</dcterms:description>
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                          <semsim:hasPhysicalDefinition rdf:resource="http://identifiers.org/fma/FMA:63842" />
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                      </ro:part_of>
                      <semsim:name>IP3 Ca channel</semsim:name>
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              </semsim:hasMediatorParticipant>
              <semsim:hasSinkParticipant>
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              <semsim:name>Ca flow from endoplasmic reticulum to cytoplasm in cell 2</semsim:name>
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      </semsim:isComputationalComponentFor>
      <dcterms:description>Ca flow through the IP3 receptor in cell 2</dcterms:description>
    </rdf:Description>
    <rdf:Description rdf:about="#h1.phi1_c1">
      <dcterms:description>Rate of change in IP3 receptors from the closed state to open state in cell 1</dcterms:description>
    </rdf:Description>
    <rdf:Description rdf:about="#j_receptor.h2">
      <dcterms:description>Cell 2 active IP3 receptors on the endoplasmic reticulum in the open and shut states</dcterms:description>
    </rdf:Description>
    <rdf:Description rdf:about="http://www.cellml.org/cellml/1.0">
      <dc:publisher>The University of Auckland, Auckland Bioengineering Institute</dc:publisher>
      <cmeta:comment>
        <rdf:Description rdf:about="rdf:#f35cccde-ccfe-4150-8232-0c57ac47865f">
          <dc:creator>
            <rdf:Description rdf:about="rdf:#49c5a7c9-2c51-4e11-92ea-47cd30b4e70b">
              <vCard:FN>James Lawson</vCard:FN>
            </rdf:Description>
          </dc:creator>
          <rdf:value>This model has been curated and is known to run in PCEnv. The model is able to produce oscillating output similar to that shown in figures from the publication.</rdf:value>
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      </cmeta:comment>
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              <vCard:Orgname>The University of Auckland</vCard:Orgname>
              <vCard:Orgunit>Auckland Bioengineering Institute</vCard:Orgunit>
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          <rdf:value>Fixed duplicate connections

Fixed CellML 1.0/1.1 namespace mixing

Updated documentation, curation status</rdf:value>
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      <cmeta:modification>
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          <rdf:value>Recoded model using parameters used by Biomodels Database as a guide</rdf:value>
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      <dcterms:description>Rate of change in IP3 receptors from the closed state to inactive state in cell 1</dcterms:description>
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    <rdf:Description rdf:about="#bindschadler_2001" semsim:modelId="bindschadler_sneyd_2001" semsim:AnnotatorContactInfo="thompsct@umich.edu" semsim:modelName="bindschadler_sneyd_2001">
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      <dcterms:description>Cell 2 Ca concentration in the cytoplasm</dcterms:description>
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    <rdf:Description rdf:about="#c2.j_diffusion">
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      <dcterms:description>Constant for rate equation represented by phi 2</dcterms:description>
    </rdf:Description>
    <rdf:Description rdf:about="#j_receptor.phi1_c1">
      <dcterms:description>Rate of change in IP3 receptors from the closed state to open state in cell 1</dcterms:description>
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    <rdf:Description rdf:about="#phi.c2">
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      <dcterms:description>Cell 2 Ca concentration in the cytoplasm</dcterms:description>
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    <rdf:Description rdf:about="#model_parameters.Vp">
      <dcterms:description>Constant for calculation of Ca flow via ATPase pumps</dcterms:description>
    </rdf:Description>
    <rdf:Description rdf:about="#j_receptor.h1">
      <dcterms:description>Cell 1 active IP3 receptors on the endoplasmic reticulum in the open and shut states</dcterms:description>
    </rdf:Description>
    <rdf:Description rdf:about="#j_receptor.phi_1_c1">
      <dcterms:description>Rate of change in IP3 receptors from the open state to closed state in cell 1</dcterms:description>
    </rdf:Description>
    <rdf:Description rdf:about="#h1.phi3_c1">
      <dcterms:description>Rate of change in IP3 receptors from the inactive state to open state in cell 1</dcterms:description>
    </rdf:Description>
    <rdf:Description rdf:about="#h2.h2">
      <dcterms:description>Cell 2 active IP3 receptors on the endoplasmic reticulum in the open and shut states</dcterms:description>
    </rdf:Description>
  </rdf:RDF>
</model>