Kinetics of in vitro natural killer activity against K562 cells as detected by flow cytometry

Loris Zamai, Adriana R. Mariani, Giorgio Zauli, Luigi Rodella, Rita Rezzani, Francesco A. Manzoli, Marco Vitale

Research output: Contribution to journalArticle

24 Citations (Scopus)

Abstract

Natural killer (NK) cells bind to K562 tumor target cells in vitro and kill them. The binding and cytotoxic activities of NK cells are tightly related to each other: degranulation of the cytotoxic effector is the basis for target cell damage and a consequence of effector-target recognition and binding. However, the two phases of NK activity, binding and killing, have always been measured separately by various methodologies and under different experimental conditions, because of the lack of a comprehensive methodology able to measure both of them at one time. Here we describe the simultaneous measurement of the binding and killing activities against K562 of resting and cytokine (IL-2 or IL-12)-stimulated NK cells by flow cytometry. NK, K562 and conjugates can be identified and measured by flow cytometry on the basis of NK mAb staining and target cells autofluorescence (Binding Plot). Within each population of the binding plot, killed targets can be identified and measured by their scatter characteristics (Cytotoxicity Plot). We show that i) the conjugate formation is enhanced in cytokine-stimulated cells, even at relatively short co-incubation times; ii) the conjugate release is also accelerated by cytokines; iii) the conjugate release is always quicker than the induction of the morphological changes in the target cell that generate its modified scattering properties.

Original languageEnglish
Pages (from-to)280-285
Number of pages6
JournalCytometry
Volume32
Issue number4
DOIs
Publication statusPublished - Aug 1 1998

Fingerprint

K562 Cells
Flow Cytometry
Natural Killer Cells
Cytokines
Interleukin-12
Interleukin-2
In Vitro Techniques
Staining and Labeling
Population
Neoplasms

Keywords

  • Binding
  • Cytotoxicity
  • Flow cytometry
  • IL-12
  • IL-2
  • NK cells

ASJC Scopus subject areas

  • Biophysics
  • Cell Biology
  • Endocrinology
  • Hematology
  • Pathology and Forensic Medicine

Cite this

Zamai, L., Mariani, A. R., Zauli, G., Rodella, L., Rezzani, R., Manzoli, F. A., & Vitale, M. (1998). Kinetics of in vitro natural killer activity against K562 cells as detected by flow cytometry. Cytometry, 32(4), 280-285. https://doi.org/10.1002/(SICI)1097-0320(19980801)32:4<280::AID-CYTO4>3.0.CO;2-M

Kinetics of in vitro natural killer activity against K562 cells as detected by flow cytometry. / Zamai, Loris; Mariani, Adriana R.; Zauli, Giorgio; Rodella, Luigi; Rezzani, Rita; Manzoli, Francesco A.; Vitale, Marco.

In: Cytometry, Vol. 32, No. 4, 01.08.1998, p. 280-285.

Research output: Contribution to journalArticle

Zamai, L, Mariani, AR, Zauli, G, Rodella, L, Rezzani, R, Manzoli, FA & Vitale, M 1998, 'Kinetics of in vitro natural killer activity against K562 cells as detected by flow cytometry', Cytometry, vol. 32, no. 4, pp. 280-285. https://doi.org/10.1002/(SICI)1097-0320(19980801)32:4<280::AID-CYTO4>3.0.CO;2-M
Zamai, Loris ; Mariani, Adriana R. ; Zauli, Giorgio ; Rodella, Luigi ; Rezzani, Rita ; Manzoli, Francesco A. ; Vitale, Marco. / Kinetics of in vitro natural killer activity against K562 cells as detected by flow cytometry. In: Cytometry. 1998 ; Vol. 32, No. 4. pp. 280-285.
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