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          <dc:contributor>Wang, Fei</dc:contributor>
          <dc:contributor>Belmont, Andrew S.</dc:contributor>
          <dc:contributor>Wang, Fei</dc:contributor>
          <dc:contributor>Chen, Jie</dc:contributor>
          <dc:contributor>Newmark, Phillip A.</dc:contributor>
          <dc:contributor>Xiang, Yang</dc:contributor>
          <dc:creator>Shin, Myung Eun</dc:creator>
          <dc:date>2012-02-01T00:49:57Z</dc:date>
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          <dc:date>2012-02-01T00:49:57Z</dc:date>
          <dc:date>2011-12</dc:date>
          <dc:description>Despite recent advances in our understanding of biochemical regulation of neutrophil
chemotaxis, little is known about how mechanical factors control neutrophils’ persistent polarity and rapid motility. Here, by using a human neutrophil-like cell line and human primary neutrophils, we describe a dynamic spatiotemporal pattern of tractions in neutrophils during chemotaxis. Tractions are located at both the leading and the trailing edge of neutrophils, where they oscillate with a defined periodicity. Interestingly, traction oscillations at the leading and the trailing edge are out of phase with the tractions at the front leading those at the back, suggesting a temporal mechanism that coordinates leading
edge and trailing edge activities. The magnitude and periodicity of tractions depend upon the activity of non-muscle myosin IIA. Specifically, traction development at the leading edge requires myosin light chain kinase (MLCK)-mediated myosin II contractility and is
necessary for α5β1-integrin activation and leading edge adhesion. Localized myosin II
activation induced by spatially activated small GTPase Rho and its downstream kinase p160-ROCK, as previously reported, leads to contraction of actin-myosin II complexes at the trailing edge, causing it to de-adhere. Our data identify a key biomechanical
mechanism for persistent cell polarity and motility.</dc:description>
          <dc:description>Item withdrawn by Mark Zulauf (zulauf@illinois.edu) on 2011-08-19T15:24:07Z
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Item is restricted until 2014-02-01T00:50:07Z</dc:description>
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          <dc:identifier>http://hdl.handle.net/2142/29509</dc:identifier>
          <dc:language>en</dc:language>
          <dc:rights>Copyright 2011 Myung Eun Shin</dc:rights>
          <dc:subject>Neutrophil Chemotaxis</dc:subject>
          <dc:subject>Traction</dc:subject>
          <dc:subject>Myosin-Light-Chain Kinase</dc:subject>
          <dc:subject>Myosin Type II</dc:subject>
          <dc:subject>Cell Adhesion</dc:subject>
          <dc:subject>Cell Motility</dc:subject>
          <dc:subject>Mechanotransduction</dc:subject>
          <dc:title>Spatiotemporal organization, regulation and function of traction during neutrophil chemotaxis</dc:title>
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            <departmentCode>1584</departmentCode>
            <discipline>Cell and Developmental Biology</discipline>
            <disciplineCode>4094</disciplineCode>
            <grantor>University of Illinois at Urbana-Champaign</grantor>
            <level>Dissertation</level>
            <name>Ph.D.</name>
            <program>PHD:Cell&amp;Develpmntl Biol -UIUC</program>
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