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  <title><![CDATA[PhD Defense by Allison Ramey-Ward]]></title>
  <body><![CDATA[<p><strong>Allison Ramey-Ward</strong></p>

<p><strong>PhD Thesis Defense Presentation</strong></p>

<p>&nbsp;</p>

<p><strong>Date:</strong> Tuesday, August 17<sup>th</sup>, 2021</p>

<p><strong>Time:</strong> 10:00 am to 12:00 pm</p>

<p><strong>Location:</strong> Atwood Chemistry Room 360 (Emory)</p>

<p><strong>Remote Location:</strong> <a href="https://emory.zoom.us/j/96016166045">https://emory.zoom.us/j/96016166045</a></p>

<p>&nbsp;</p>

<p><strong>Committee Members: </strong></p>

<p>Khalid Salaita, PhD (advisor)</p>

<p>Andres Garcia, PhD</p>

<p>Johnna Temenoff, PhD</p>

<p>Young Jang, PhD</p>

<p>Jarrod Call, PhD (UGA Dept. Kinesiology)</p>

<p>&nbsp;</p>

<p><strong>Title:</strong> Development of a mechanically active hydrogel biomaterial for muscle tissue engineering</p>

<p>&nbsp;</p>

<p><strong>Abstract: </strong></p>

<p>&nbsp;</p>

<p>Skeletal muscle cells exist in the body in highly mechanically dynamic environments, applying forces to the extracellular matrix (ECM) and experiencing&nbsp; extracellular forces transmitted back to them via cell adhesion receptors such as integrins. These forces have been demonstrated <em>in vivo </em>and clinically to be critical to normal muscle growth and function, yet the incorporation of mechanics into the study of muscle cell biology has been limited, due at least in part to the need for complex instrumentation to apply such forces to cell culture systems. To this end, we develop novel methods for mechanically dynamic cell culture in 2D and 2.5D using a near infrared (NIR) light-actuated mechanism: the optomechanical actuator (OMA). OMAs are photothermally responsive nanoparticles that shrink in size when illuminated with NIR light.</p>

<p>&nbsp;</p>

<p>In Aim 1, we create a cell culture surface of OMAs modified with cell adhesion ligands, and use these responsive 2D surfaces to show unprecedented spatiotemporal resolution of myoblast mechanical stimulation, demonstrating enhancement of myogenic markers after shorter stimulation time and length scales than previously reported in by other methods. In Aim 2, we further develop this technique, developing a composite, mechanically active hydrogel biomaterial by conferring NIR responsivity to a biopolymer matrix of gelatin and laminin through the incorporation of OMAs. We demonstrate this ability of this material to enhance myogenesis in myoblast cell culture, as well as to&nbsp; mimic the beneficial effects of exercise <em>in vitro </em>in a chronic inflammation model. This thesis has resulted in novel methods and materials for the application of dynamic forces <em>in vitro</em>, which have broad future applications in cell biology and tissue engineering.</p>

<p>&nbsp;</p>
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