Multi-cellular natural killer (NK) cell clusters enhance NK cell activation through localizing IL-2 within the cluster

Miju Kim, Tae Jin Kim, Hye Mi Kim, Junsang Doh, Kyung-Mi Lee

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

Multi-cellular cluster formation of natural killer (NK) cells occurs during in vivo priming and potentiates their activation to IL-2. However, the precise mechanism underlying this synergy within NK cell clusters remains unclear. We employed lymphocyte-laden microwell technologies to modulate contact-mediated multi-cellular interactions among activating NK cells and to quantitatively assess the molecular events occurring in multi-cellular clusters of NK cells. NK cells in social microwells, which allow cell-to-cell contact, exhibited significantly higher levels of IL-2 receptor (IL-2R) signaling compared with those in lonesome microwells, which prevent intercellular contact. Further, CD25, an IL-2R α chain, and lytic granules of NK cells in social microwells were polarized toward MTOC. Live cell imaging of lytic granules revealed their dynamic and prolonged polarization toward neighboring NK cells without degranulation. These results suggest that IL-2 bound on CD25 of one NK cells triggered IL-2 signaling of neighboring NK cells. These results were further corroborated by findings that CD25-KO NK cells exhibited lower proliferation than WT NK cells, and when mixed with WT NK cells, underwent significantly higher level of proliferation. These data highlights the existence of IL-2 trans-presentation between NK cells in the local microenvironment where the availability of IL-2 is limited.

Original languageEnglish
Article number40623
JournalScientific Reports
Volume7
DOIs
Publication statusPublished - 2017 Jan 11

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Natural Killer Cells
Interleukin-2
Interleukin-2 Receptors
Microtubule-Organizing Center
Cell Degranulation
Lymphocytes
Technology

ASJC Scopus subject areas

  • General

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Multi-cellular natural killer (NK) cell clusters enhance NK cell activation through localizing IL-2 within the cluster. / Kim, Miju; Kim, Tae Jin; Kim, Hye Mi; Doh, Junsang; Lee, Kyung-Mi.

In: Scientific Reports, Vol. 7, 40623, 11.01.2017.

Research output: Contribution to journalArticle

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