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  <title><![CDATA[PhD Defense by Shereka Banton]]></title>
  <body><![CDATA[<p><strong>Shereka Banton<br />
BME PhD&nbsp;Defense&nbsp;Presentation</strong><br />
March 7th, 2017 at 9 am<br />
Manufacturing&nbsp;Related Disciplines Complex (MRDC), Rm 3403<br />
&nbsp;<br />
Thesis Committee Members:<br />
Gilda Barabino, PhD (Advisor)<br />
Michael Davis, PhD (Co-advisor)<br />
Wilbur Lam, MD-PhD<br />
Philip Santangelo, PhD<br />
Betty Pace, MD</p>

<p>Abdullah Kutlar, MD</p>

<p>Lakeshia Taite, PhD<br />
&nbsp;<br />
<strong>Human Peripheral Reticulocyte Isolation and Exosome Release&nbsp;<em>in vitro</em></strong><br />
<br />
The exosomes released by peripheral reticulocytes were originally thought to function as vehicles for protein clearance for the maturing cells.&nbsp; With the emergence of exosomes as mediators of intercellular communication, a new paradigm exists for the role of reticulocyte-derived exosomes in both healthy and disease states, particularly conditions whose pathology is driven by the red blood and its precursors.&nbsp; However, no standard or detailed method for the isolation of human peripheral CD71<sup>+</sup>&nbsp;reticulocytes exists.&nbsp; A combination of density-dependent and immunomagnetic approaches was&nbsp;used to demonstrate a procedure to isolate human CD71<sup>+</sup>&nbsp;reticulocytes from peripheral blood. Nearly 90% of the CD71<sup>+</sup>&nbsp;cells were distinct from the CD71<sup>-</sup>&nbsp;population when measured with flow cytometry detection of RNA.&nbsp; CD71<sup>+</sup>&nbsp;reticulocyte-derived exosomes were then isolated and&nbsp;analyzed after incubation&nbsp;<em>in vitro</em>,&nbsp;the first such demonstration of these phenomena using these cells.&nbsp; These findings form the basis for more targeted and mechanistic studies into the role of reticulocyte-derived exosomes in pathologies like sickle cell disease.</p>
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