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Inhibitory receptors alter natural killer cell interactions with target cells yet allow simultaneous killing of susceptible targets
Umeå University, Faculty of Science and Technology, Umeå Centre for Molecular Pathogenesis (UCMP).
Umeå University, Faculty of Science and Technology, Department of Physics.
Umeå University, Faculty of Science and Technology, Department of Physics.
Umeå University, Faculty of Science and Technology, Department of Physics.ORCID iD: 0000-0002-8580-9700
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1999 (English)In: Journal of Experimental Medicine, ISSN 0022-1007, E-ISSN 1540-9538, Vol. 190, no 7, p. 1005-1012Article in journal (Refereed) Published
Abstract [en]

Inhibitory receptors expressed on natural killer (NK) cells abrogate positive signals upon binding corresponding major histocompatibility complex (MHC) class I molecules on various target cells. By directly micromanipulating the effector-target cell encounter using an optical tweezers system which allowed temporal and spatial control, we demonstrate that Ly49-MHC class I interactions prevent characteristic cellular responses in NK cells upon binding to target cells. Furthermore, using this system, we directly demonstrate that an NK cell already bound to a resistant target cell may simultaneously bind and kill a susceptible target cell. Thus, although Ly49-mediated inhibitory signals can prevent many types of effector responses, they do not globally inhibit cellular function, but rather the inhibitory signal is spatially restricted towards resistant targets.

Place, publisher, year, edition, pages
Rockefeller University Press, 1999. Vol. 190, no 7, p. 1005-1012
Keywords [en]
natural killer cell, major histocompatibility complex class I, optical tweezers, Ly49, video microscopy
National Category
Immunology in the medical area
Identifiers
URN: urn:nbn:se:umu:diva-224891DOI: 10.1084/jem.190.7.1005ISI: 000083021700013PubMedID: 10510090Scopus ID: 2-s2.0-0033523620OAI: oai:DiVA.org:umu-224891DiVA, id: diva2:1860485
Available from: 2024-05-24 Created: 2024-05-24 Last updated: 2024-05-24Bibliographically approved

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Fällman, ErikAxner, Ove

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CiteExportLink to record
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