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Identification of mediators of T-cell receptor signaling via the screening of chemical inhibitor libraries

*Corresponding author for this work
  • National University of Singapore
    ,
  • Agency for Science, Technology and Research, Singapore
    ,
  • Curiox Biosystems
    ,
  • KU Leuven
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

The T-cell receptor (TCR) signaling pathway comprises a multitude of mediators that transmit signals upon the activation of the TCR. Different strategies have been proposed and implemented for the identification of new mediators of TCR signaling, which would improve the understanding of T-cell processes, including activation and thymic selection. We describe a screening assay that enables the identification of molecules that influence TCR signaling based on the activation of developing thymocytes. Strong TCR signals cause developing thymocytes to activate apoptotic machinery in a process known as negative selection. Through the application of kinase inhibitors, those with targets that affect TCR signaling are able to override the process of negative selection. The method detailed in this paper can be used to identify inhibitors of canonical kinases with established roles in the TCR signaling pathways and also inhibitors of new kinases yet to be established in the TCR signaling pathways. The screening strategy here can be applied to screens of higher throughput for the identification of novel druggable targets in TCR signaling.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Article number

e58946

Journal (Volume, Issue Number)

Journal of Visualized Experiments (Volume 2019, Issue 143)

Publication milestones

  • Published - 01/2019

Publication status

Published - 01/2019

ISSN

1940-087X

Publication IDs

  • Scopus: 85061227863
  • PubMed: 30735195

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Funding Details

This work was supported by grants from the Singapore Ministry of Health's National Medical Research Council, NMRC CBRG15may017, and the Singapore Ministry of Education, 2014-T2-1-136 (to N.R.J.G.).
FundersFunding numbers
NMRC
CBRG15may017, 2014-T2-1-136
MOH
-
MOE
-