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  <title><![CDATA[Young Innovators in Biomedical Engineering]]></title>
  <body><![CDATA[<p><strong>"Single-cell Secretion Analysis Reveals Paracrine Strategies for Coordinating Innate Immune Responses in Cell Populations"</strong><br /> <br /> <strong>Kathryn Miller-Jensen, PhD</strong><strong><br /> </strong><strong>Assistant Professor, Department of Biomedical Engineering</strong><strong><br /> </strong><strong>Yale University</strong><br /> &nbsp; <br /> Seminar will be made available via videoconference in the Health Sciences Research Building, room E182 and Technology Enterprise Park, room 104.<br /> <br /> Cell responses are mediated by intermediate signals that are secreted and sensed by the same cells and are subject to significant cell-to-cell heterogeneity. The propagation of these intermediate signals by extracellular signaling impacts the collective cell-population response, but the contribution of autocrine versus paracrine signaling is difficult to analyze. To address this, we have combined multiplexed, microwell single-cell secretion measurements with cell-population data to uncover the role of paracrine signaling in shaping the inflammatory response in human macrophages following toll-like receptor 4 (TLR4) stimulation with lipopolysaccharide (LPS). We demonstrate that loss of paracrine signaling upon single-cell isolation in microwells significantly alters secretion of some LPS-stimulated cytokines. Gaussian graphical models of these single-cell “perturbation” data sets specifically uncover regulatory connections between cytokines in the LPS-stimulated network. Tumor necrosis factor-α (TNF), the most highly connected cytokine in the network, exhibits highly heterogeneous secretion, such that a small fraction of cells appears to drive total TNF output in the cell population. Using a mechanistic ODE model fit to our single-cell data, we demonstrate that this small fraction of high TNF secretors combined with positive feedback amplifies the pro-inflammatory IL-6 response in cell populations. Overall, our results reveal a novel role for paracrine cell-to-cell communication in coordinating a rapid and reliable innate immune response in spite of underlying cell-to-cell heterogeneity.&nbsp; <br /> <br /> <a href="https://www.bme.gatech.edu/bme/faculty/Melissa-Kemp" target="_blank">Melissa Kemp, PhD</a> - faculty host</p><p>&nbsp;</p>]]></body>
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      <value><![CDATA["Single-cell Secretion Analysis Reveals Paracrine Strategies for Coordinating Innate Immune Responses in Cell Populations" - Kathryn Miller-Jensen, PhD - Yale University]]></value>
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      <value><![CDATA[<p>Young Innovators in Biomedical Engineering - "Single-cell Secretion Analysis Reveals Paracrine Strategies for Coordinating Innate Immune Responses in Cell Populations" - Kathryn Miller-Jensen, PhD - Yale University</p>]]></value>
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      <value><![CDATA[2014-11-25T10:00:00-05:00]]></value>
      <value2><![CDATA[2014-11-25T11:00:00-05:00]]></value2>
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      <timezone><![CDATA[America/New_York]]></timezone>
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        <value><![CDATA[Undergraduate students]]></value>
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        <value><![CDATA[Faculty/Staff]]></value>
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        <value><![CDATA[Public]]></value>
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        <value><![CDATA[Graduate students]]></value>
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      <value><![CDATA[<p><a href="mailto:melissa.kemp@bme.gatech.edu">Melissa Kemp, PhD</a> - faculty host</p>]]></value>
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      <value><![CDATA[(404) 385-0124]]></value>
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      <url><![CDATA[http://www.bme.gatech.edu]]></url>
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        <url>http://seas.yale.edu/faculty-research/faculty-directory/kathryn-miller-jensen</url>
        <link_title><![CDATA[Miller-Jensen profile]]></link_title>
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          <item><![CDATA[Wallace H. Coulter Dept. of Biomedical Engineering]]></item>
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        <value><![CDATA[Biomedical Engieering]]></value>
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        <value><![CDATA[Young Innovators]]></value>
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