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Live Imaging of Influenza Infection of the Trachea Reveals Dynamic Regulation of CD8+ T Cell Motility by Antigen
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نویسنده
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lambert emo k. ,hyun y.-m. ,reilly e. ,barilla c. ,gerber s. ,fowell d. ,kim m. ,topham d.j.
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منبع
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plos pathogens - 2016 - دوره : 12 - شماره : 9
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چکیده
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During a primary influenza infection,cytotoxic cd8+ t cells need to infiltrate the infected airways and engage virus-infected epithelial cells. the factors that regulate t cell motility in the infected airway tissue are not well known. to more precisely study t cell infiltration of the airways,we developed an experimental model system using the trachea as a site where live imaging can be performed. cd8+ t cell motility was dynamic with marked changes in motility on different days of the infection. in particular,significant changes in average cell velocity and confinement were evident on days 8–10 during which the t cells abruptly but transiently increase velocity on day 9. experiments to distinguish whether infection itself or antigen affect motility revealed that it is antigen,not active infection per se that likely affects these changes as blockade of peptide/mhc resulted in increased velocity. these observations demonstrate that influenza tracheitis provides a robust experimental foundation to study molecular regulation of t cell motility during acute virus infection. © 2016 lambert emo et al.
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آدرس
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david h. smith center for vaccine biology & immunology,university of rochester school of medicine and dentistry,rochester,ny,united states,department of microbiology & immunology,university of rochester school of medicine and dentistry,rochester,ny, United States, david h. smith center for vaccine biology & immunology,university of rochester school of medicine and dentistry,rochester,ny,united states,department of microbiology & immunology,university of rochester school of medicine and dentistry,rochester,ny,united states,department of anatomy,yonsei university college of medicine,seoul, South Korea, david h. smith center for vaccine biology & immunology,university of rochester school of medicine and dentistry,rochester,ny,united states,department of microbiology & immunology,university of rochester school of medicine and dentistry,rochester,ny, United States, david h. smith center for vaccine biology & immunology,university of rochester school of medicine and dentistry,rochester,ny,united states,department of microbiology & immunology,university of rochester school of medicine and dentistry,rochester,ny, United States, department of surgery,university of rochester school of medicine and dentistry,rochester,ny, United States, david h. smith center for vaccine biology & immunology,university of rochester school of medicine and dentistry,rochester,ny,united states,department of microbiology & immunology,university of rochester school of medicine and dentistry,rochester,ny, United States, david h. smith center for vaccine biology & immunology,university of rochester school of medicine and dentistry,rochester,ny,united states,department of microbiology & immunology,university of rochester school of medicine and dentistry,rochester,ny, United States, david h. smith center for vaccine biology & immunology,university of rochester school of medicine and dentistry,rochester,ny,united states,department of microbiology & immunology,university of rochester school of medicine and dentistry,rochester,ny, United States
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Authors
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