دورية أكاديمية

Control of immune ligands by members of a cytomegalovirus gene expansion suppresses natural killer cell activation

التفاصيل البيبلوغرافية
العنوان: Control of immune ligands by members of a cytomegalovirus gene expansion suppresses natural killer cell activation
المؤلفون: Fielding, Ceri A, Weekes, Michael P, Nobre, Luis V, Ruckova, Eva, Wilkie, Gavin S, Paulo, Joao A, Chang, Chiwen, Suárez, Nicolás M, Davies, James A, Antrobus, Robin, Stanton, Richard J, Aicheler, Rebecca J, Nichols, Hester, Vojtesek, Borek, Trowsdale, John, Davison, Andrew J, Gygi, Steven P, Tomasec, Peter, Lehner, Paul J, Wilkinson, Gavin W G
المصدر: Fielding, C. A., M. P. Weekes, L. V. Nobre, E. Ruckova, G. S. Wilkie, J. A. Paulo, C. Chang, et al. 2017. “Control of immune ligands by members of a cytomegalovirus gene expansion suppresses natural killer cell activation.” eLife 6 (1): e22206. doi:10.7554/eLife.22206. http://dx.doi.org/10.7554/eLife.22206.
بيانات النشر: eLife Sciences Publications, Ltd, 2017.
سنة النشر: 2017
المجموعة: HMS Scholarly Articles
مصطلحات موضوعية: cytomegalovirus, human, immune evasion, natural killer cell, Virus
الوصف: The human cytomegalovirus (HCMV) US12 family consists of ten sequentially arranged genes (US12-21) with poorly characterized function. We now identify novel natural killer (NK) cell evasion functions for four members: US12, US14, US18 and US20. Using a systematic multiplexed proteomics approach to quantify ~1300 cell surface and ~7200 whole cell proteins, we demonstrate that the US12 family selectively targets plasma membrane proteins and plays key roles in regulating NK ligands, adhesion molecules and cytokine receptors. US18 and US20 work in concert to suppress cell surface expression of the critical NKp30 ligand B7-H6 thus inhibiting NK cell activation. The US12 family is therefore identified as a major new hub of immune regulation. DOI: http://dx.doi.org/10.7554/eLife.22206.001
نوع الوثيقة: Journal Article
اللغة: English
Relation: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5367895/pdf/; eLife
DOI: 10.7554/eLife.22206
URL الوصول: http://nrs.harvard.edu/urn-3:HUL.InstRepos:32071983
حقوق: open
URL: http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
رقم الأكسشن: edshld.1.32071983
قاعدة البيانات: Digital Access to Scholarship at Harvard (DASH)