Antigen discrimination by T cells relies on size-constrained microvillar contact

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作者
Edward Jenkins
Markus Körbel
Caitlin O’Brien-Ball
James McColl
Kevin Y. Chen
Mateusz Kotowski
Jane Humphrey
Anna H. Lippert
Heather Brouwer
Ana Mafalda Santos
Steven F. Lee
Simon J. Davis
David Klenerman
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[1] University of Oxford,Radcliffe Department of Medicine, John Radcliffe Hospital
[2] University of Oxford,Medical Research Council Human Immunology Unit, John Radcliffe Hospital
[3] University of Cambridge,Yusuf Hamied Department of Chemistry
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T cells use finger-like protrusions called ‘microvilli’ to interrogate their targets, but why they do so is unknown. To form contacts, T cells must overcome the highly charged, barrier-like layer of large molecules forming a target cell’s glycocalyx. Here, T cells are observed to use microvilli to breach a model glycocalyx barrier, forming numerous small (<0.5 μm diameter) contacts each of which is stabilized by the small adhesive protein CD2 expressed by the T cell, and excludes large proteins including CD45, allowing sensitive, antigen dependent TCR signaling. In the absence of the glycocalyx or when microvillar contact-size is increased by enhancing CD2 expression, strong signaling occurs that is no longer antigen dependent. Our observations suggest that, modulated by the opposing effects of the target cell glycocalyx and small adhesive proteins, the use of microvilli equips T cells with the ability to effect discriminatory receptor signaling.
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