Microchip screening platform for single cell assessment of NK cell cytotoxicity

Here we report a screening platform for assessment of the cytotoxic potential of individual natural killer (NK) cells within larger populations. Human primary NK cells were distributed across a silicon-glass microchip containing 32 400 individual microwells loaded with target cells. Through fluoresc...

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Main Authors: Karolin eGuldevall, Ludwig eBrandt, Elin eForslund, Karl eOlofsson, Thomas Wilhelm Frisk, Per Erik Olofsson, Karin eGustafsson, Bruno eVanherberghen, Otto eManneberg, Hjalmar eBrismar, Klas eKärre, Michael eUhlin, Björn eÖnfelt
Format: Article
Language:English
Published: Frontiers Media S.A. 2016-04-01
Series:Frontiers in Immunology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fimmu.2016.00119/full
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spelling doaj-45acf1b43916466890eb937445129a752020-11-24T23:41:24ZengFrontiers Media S.A.Frontiers in Immunology1664-32242016-04-01710.3389/fimmu.2016.00119182848Microchip screening platform for single cell assessment of NK cell cytotoxicityKarolin eGuldevall0Ludwig eBrandt1Elin eForslund2Elin eForslund3Karl eOlofsson4Thomas Wilhelm Frisk5Per Erik Olofsson6Karin eGustafsson7Bruno eVanherberghen8Otto eManneberg9Hjalmar eBrismar10Klas eKärre11Michael eUhlin12Michael eUhlin13Björn eÖnfelt14Björn eÖnfelt15Science for Life LaboratoryScience for Life LaboratoryScience for Life LaboratoryKarolinska InstitutetScience for Life LaboratoryScience for Life LaboratoryScience for Life LaboratoryScience for Life LaboratoryScience for Life LaboratoryScience for Life LaboratoryScience for Life LaboratoryKarolinska InstitutetCenter for Allogeneic Stem Cell Transplantation, Huddinge University Hospital at the Karolinska InstituteKarolinska InstitutetScience for Life LaboratoryKarolinska InstitutetHere we report a screening platform for assessment of the cytotoxic potential of individual natural killer (NK) cells within larger populations. Human primary NK cells were distributed across a silicon-glass microchip containing 32 400 individual microwells loaded with target cells. Through fluorescence screening and automated image analysis the numbers of NK and live or dead target cells in each well could be assessed at different time points after initial mixing. Cytotoxicity was also studied by time-lapse live-cell imaging in microwells quantifying the killing potential of individual NK cells. Although most resting NK cells (≈75%) were non-cytotoxic against the leukemia cell line K562, some NK cells were able to kill several (≥3) target cells within the 12 hours long experiment. In addition, the screening approach was adapted to increase the chance to find and evaluate serial killing NK cells. Even if the cytotoxic potential varied between donors it was evident that a small fraction of highly cytotoxic NK cells were responsible for a substantial portion of the killing. We demonstrate multiple assays where our platform can be used to enumerate and characterize cytotoxic cells, such as NK or T cells. This approach could find use in clinical applications, e.g. in the selection of donors for stem cell transplantation or generation of highly specific and cytotoxic cells for adoptive immunotherapy.http://journal.frontiersin.org/Journal/10.3389/fimmu.2016.00119/fullMicroscopy, FluorescenceNK cellsscreeningCytotoxicityimmune synapsesingle cell analysis
collection DOAJ
language English
format Article
sources DOAJ
author Karolin eGuldevall
Ludwig eBrandt
Elin eForslund
Elin eForslund
Karl eOlofsson
Thomas Wilhelm Frisk
Per Erik Olofsson
Karin eGustafsson
Bruno eVanherberghen
Otto eManneberg
Hjalmar eBrismar
Klas eKärre
Michael eUhlin
Michael eUhlin
Björn eÖnfelt
Björn eÖnfelt
spellingShingle Karolin eGuldevall
Ludwig eBrandt
Elin eForslund
Elin eForslund
Karl eOlofsson
Thomas Wilhelm Frisk
Per Erik Olofsson
Karin eGustafsson
Bruno eVanherberghen
Otto eManneberg
Hjalmar eBrismar
Klas eKärre
Michael eUhlin
Michael eUhlin
Björn eÖnfelt
Björn eÖnfelt
Microchip screening platform for single cell assessment of NK cell cytotoxicity
Frontiers in Immunology
Microscopy, Fluorescence
NK cells
screening
Cytotoxicity
immune synapse
single cell analysis
author_facet Karolin eGuldevall
Ludwig eBrandt
Elin eForslund
Elin eForslund
Karl eOlofsson
Thomas Wilhelm Frisk
Per Erik Olofsson
Karin eGustafsson
Bruno eVanherberghen
Otto eManneberg
Hjalmar eBrismar
Klas eKärre
Michael eUhlin
Michael eUhlin
Björn eÖnfelt
Björn eÖnfelt
author_sort Karolin eGuldevall
title Microchip screening platform for single cell assessment of NK cell cytotoxicity
title_short Microchip screening platform for single cell assessment of NK cell cytotoxicity
title_full Microchip screening platform for single cell assessment of NK cell cytotoxicity
title_fullStr Microchip screening platform for single cell assessment of NK cell cytotoxicity
title_full_unstemmed Microchip screening platform for single cell assessment of NK cell cytotoxicity
title_sort microchip screening platform for single cell assessment of nk cell cytotoxicity
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2016-04-01
description Here we report a screening platform for assessment of the cytotoxic potential of individual natural killer (NK) cells within larger populations. Human primary NK cells were distributed across a silicon-glass microchip containing 32 400 individual microwells loaded with target cells. Through fluorescence screening and automated image analysis the numbers of NK and live or dead target cells in each well could be assessed at different time points after initial mixing. Cytotoxicity was also studied by time-lapse live-cell imaging in microwells quantifying the killing potential of individual NK cells. Although most resting NK cells (≈75%) were non-cytotoxic against the leukemia cell line K562, some NK cells were able to kill several (≥3) target cells within the 12 hours long experiment. In addition, the screening approach was adapted to increase the chance to find and evaluate serial killing NK cells. Even if the cytotoxic potential varied between donors it was evident that a small fraction of highly cytotoxic NK cells were responsible for a substantial portion of the killing. We demonstrate multiple assays where our platform can be used to enumerate and characterize cytotoxic cells, such as NK or T cells. This approach could find use in clinical applications, e.g. in the selection of donors for stem cell transplantation or generation of highly specific and cytotoxic cells for adoptive immunotherapy.
topic Microscopy, Fluorescence
NK cells
screening
Cytotoxicity
immune synapse
single cell analysis
url http://journal.frontiersin.org/Journal/10.3389/fimmu.2016.00119/full
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