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    <responseDate>2026-10-13T14:17:21Z</responseDate>
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                <identifier>oai:data.mendeley.com/ptschm67th.1</identifier>
                <datestamp>2025-09-01T15:41:18Z</datestamp>
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    <dc:creator>Ren, Huixia</dc:creator>
    <dc:title>Pancreatic Islet Oscillation Rhythmicity Arises from δ and α Cell Interactions</dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>This is source data for figures in &lt;&lt;Pancreatic Islet Oscillation Rhythmicity Arises from δ and α Cell Interactions&gt;&gt; study. 
1.	We developed a microfluidic chip enabling high-throughput observation of islets Ca2+ activities and their 3D composition. Our findings demonstrated that δ-α cell-to-cell interactions are the primary source of variability in glucose-induced Ca2+ oscillation patterns.
2.	Through experimental investigations, we identified a phase diagram in the oscillation modes, covering the transition from fast-to-mixed and mixed-to-slow oscillations, with increasing somatostatin or decreasing α cell mass.
3.	We proposed a mathematical model focusing on the paracrine interactions between α and δ cells. Our model depicts that fast-mixed-slow oscillation transitions as a Hopf bifurcation.
4.	Finally, we found that in vivo hypoglycemia/euglycemia induces fast Ca2+ oscillations, while hyperglycemia induces slow Ca2+ oscillations.
</dc:description>
    <dc:subject>Pancreatic Islet</dc:subject>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/ptschm67th.1</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/ptschm67th.1</dc:identifier>
    <dc:rights>Creative Commons Attribution 4.0 International</dc:rights>
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    <dc:relation>https://data.mendeley.com/datasets/ptschm67th</dc:relation>
    <dc:date>2025-09-01T15:41:18Z</dc:date>
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