Identification of Primary Natural Killer Cell Modulators by Chemical Library Screening with a Luciferase-Based Functional Assay. (January 2019)
- Record Type:
- Journal Article
- Title:
- Identification of Primary Natural Killer Cell Modulators by Chemical Library Screening with a Luciferase-Based Functional Assay. (January 2019)
- Main Title:
- Identification of Primary Natural Killer Cell Modulators by Chemical Library Screening with a Luciferase-Based Functional Assay
- Authors:
- Hayek, Simon
Bekaddour, Nassima
Besson, Laurie
Alves de Sousa, Rodolphe
Pietrancosta, Nicolas
Viel, Sébastien
Smith, Nikaia
Jacob, Yves
Nisole, Sébastien
Mandal, Rupasri
Wishart, David S.
Walzer, Thierry
Herbeuval, Jean-Philippe
Vidalain, Pierre-Olivier - Abstract:
- Natural killer (NK) cells are essential players of the innate immune response that secrete cytolytic factors and cytokines such as IFN-γ when contacting virus-infected or tumor cells. They represent prime targets in immunotherapy as defects in NK cell functions are hallmarks of many pathological conditions, such as cancer and chronic infections. The functional screening of chemical libraries or biologics would greatly help identify new modulators of NK cell activity, but commonly used methods such as flow cytometry are not easily scalable to high-throughput settings. Here we describe an efficient assay to measure the natural cytotoxicity of primary NK cells where the bioluminescent enzyme NanoLuc is constitutively expressed in the cytoplasm of target cells and is released in co-culture supernatants when lysis occurs. We fully characterized this assay using either purified NK cells or total peripheral blood mononuclear cells (PBMCs), including some patient samples, as effector cells. A pilot screen was also performed on a library of 782 metabolites, xenobiotics, and common drugs, which identified dextrometorphan and diphenhydramine as novel NK cell inhibitors. Finally, this assay was further improved by developing a dual-reporter cell line to simultaneously measure NK cell cytotoxicity and IFN-γ secretion in a single well, extending the potential of this system.
- Is Part Of:
- SLAS discovery. Volume 24:Number 1(2019)
- Journal:
- SLAS discovery
- Issue:
- Volume 24:Number 1(2019)
- Issue Display:
- Volume 24, Issue 1 (2019)
- Year:
- 2019
- Volume:
- 24
- Issue:
- 1
- Issue Sort Value:
- 2019-0024-0001-0000
- Page Start:
- 25
- Page End:
- 37
- Publication Date:
- 2019-01
- Subjects:
- natural killer cells -- luciferase -- screening -- dextromethorphan -- diphenhydramine
Drugs -- Analysis -- Periodicals
Drugs -- Testing -- Periodicals
Biomolecules -- Analysis -- Periodicals
Biomolecules -- Analysis
Drugs -- Analysis
Drugs -- Testing
Drug Evaluation, Preclinical
Molecular Biology -- methods
Periodicals
Periodicals
615.1 - Journal URLs:
- http://journals.sagepub.com/home/jbx ↗
https://www.sciencedirect.com/journal/slas-discovery/ ↗
http://www.sagepublications.com/ ↗
https://www.journals.elsevier.com/slas-discovery ↗ - DOI:
- 10.1177/2472555218797078 ↗
- Languages:
- English
- ISSNs:
- 2472-5552
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 9446.xml