<HashMap><database>biostudies-other</database><scores/><additional><omics_type>Unknown</omics_type><volume>63</volume><submitter>Lucian Smith</submitter><journal>IEEE transactions on bio-medical engineering</journal><pagination>2047-2055</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/MODEL1603110003</full_dataset_link><repository>biostudies-other</repository><additional_accession>27076052</additional_accession><pubmed_authors>Mohammad Umer Sharif Shohan</pubmed_authors><pubmed_authors>Aalap Verma</pubmed_authors><pubmed_authors>Lucian Smith</pubmed_authors></additional><is_claimable>false</is_claimable><name>Verma2016 - Ca(2+) Signal Propagation Along Hepatocyte Cords</name><description>&lt;notes xmlns="http://www.sbml.org/sbml/level2/version4">      &lt;body xmlns="http://www.w3.org/1999/xhtml">        &lt;div class="dc:title">Verma2016 - Ca(2+) Signal Propagation Along Hepatocyte Cords&lt;/div>        &lt;div class="dc:bibliographicCitation">          &lt;p>This model is described in the article:&lt;/p>          &lt;div class="bibo:title">            &lt;a href="http://identifiers.org/pubmed/27076052" title="Access to this publication">Computational Modeling of    Spatiotemporal Ca(2+) Signal Propagation Along Hepatocyte    Cords.&lt;/a>          &lt;/div>          &lt;div class="bibo:authorList">Verma A, Makadia H, Hoek JB,  Ogunnaike BA, Vadigepalli R.&lt;/div>          &lt;div class="bibo:Journal">IEEE Trans Biomed Eng 2016 Oct; 63(10):  2047-2055&lt;/div>          &lt;p>Abstract:&lt;/p>          &lt;div class="bibo:abstract">            &lt;p>The purpose of this study is to model the dynamics of    lobular Ca(2+) wave propagation induced by an extracellular    stimulus, and to analyze the effect of spatially systematic    variations in cell-intrinsic signaling parameters on sinusoidal    Ca(2+) response.We developed a computational model of lobular    scale Ca(2+) signaling that accounts for receptor- mediated    initiation of cell-intrinsic Ca(2+) signal in hepatocytes and    its propagation to neighboring hepatocytes through gap    junction-mediated molecular exchange.Analysis of the    simulations showed that a pericentral-to-periportal spatial    gradient in hormone sensitivity and/or rates of IP3 synthesis    underlies the Ca(2+) wave propagation. We simulated specific    cases corresponding to localized disruptions in the graded    pattern of these parameters along a hepatic sinusoid.    Simulations incorporating locally altered parameters exhibited    Ca(2+) waves that do not propagate throughout the hepatic    plate. Increased gap junction coupling restored normal Ca(2+)    wave propagation when hepatocytes with low Ca(2+) signaling    ability were localized in the midlobular or the pericentral    region.Multiple spatial patterns in intracellular signaling    parameters can lead to Ca(2+) wave propagation that is    consistent with the experimentally observed spatial patterns of    Ca(2+) dynamics. Based on simulations and analysis, we predict    that increased gap junction-mediated intercellular coupling can    induce robust Ca(2+) signals in otherwise poorly responsive    hepatocytes, at least partly restoring the sinusoidally    oriented Ca (2+) waves.Our bottom-up model of agonist-evoked    spatial Ca(2+) patterns can be integrated with detailed    descriptions of liver histology to study Ca(2+) regulation at    the tissue level.&lt;/p>          &lt;/div>        &lt;/div>        &lt;div class="dc:publisher">          &lt;p>This model is hosted on   &lt;a href="http://www.ebi.ac.uk/biomodels/">BioModels Database&lt;/a>  and identified by:   &lt;a href="http://identifiers.org/biomodels.db/MODEL1603110003">MODEL1603110003&lt;/a>.&lt;/p>          &lt;p>To cite BioModels Database, please use:   &lt;a href="http://identifiers.org/pubmed/20587024" title="Latest BioModels Database publication">BioModels Database:  An enhanced, curated and annotated resource for published  quantitative kinetic models&lt;/a>.&lt;/p>        &lt;/div>        &lt;div class="dc:license">          &lt;p>To the extent possible under law, all copyright and related or  neighbouring rights to this encoded model have been dedicated to  the public domain worldwide. Please refer to   &lt;a href="http://creativecommons.org/publicdomain/zero/1.0/" title="Access to: CC0 1.0 Universal (CC0 1.0), Public Domain Dedication">CC0  Public Domain Dedication&lt;/a> for more information.&lt;/p>        &lt;/div>      &lt;/body>    &lt;/notes></description><dates><release>2016-03-11T00:00:00Z</release><modification>2025-07-15T09:50:07.109Z</modification><creation>2025-03-29T21:45:22.829Z</creation></dates><accession>MODEL1603110003</accession><cross_references><biomodels___db>BIOMD0000000834</biomodels___db><pubmed>27076052</pubmed><kegg___compound>C00076</kegg___compound><ensembl>NewID</ensembl><mamo>MAMO_0000046</mamo><go>GO:0019722</go><taxonomy>9606</taxonomy><bto>BTO:0000575</bto><uniprot>P29995</uniprot><uniprot>P30560</uniprot></cross_references></HashMap>