A phenotypic screen for compounds that reverse cAMP-mediated suppression of T cell functions

SLAS Discovery

Adam Zweifach¹  Meghan Wyatt¹  David Barrett¹  Haim Bar²  Larry A. Sklar³  Mark K. Haynes³  Bruce S. Edwards³ 

[1] Department of Molecular and Cell Biology, University of Connecticut, Storrs, CT, United States;Department of Statistics, University of Connecticut, Storrs, CT, United States;University of New Mexico Center for Molecular Discovery and Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque, NM, United States;

关键词: Cancer;    Tumor microenvironment;    Immunity;    Cell signaling;   

DOI  :  

来源: DOAJ

【 摘 要 】

The solid tumor microenvironment (TME) suppresses immune responses. Three alterations in the TME converge on a pathway triggered by elevated cyclic AMP (cAMP) that suppresses T cell receptor (TCR) signaling. We developed a phenotypic assay to screen for small molecules that interfere with this pathway using TALL-104 human leukemic cytotoxic T lymphocytes pretreated with prostaglandin E2 to elevate cAMP. Beads coated with anti-CD3 antibodies stimulate lytic granule exocytosis, which is detected via binding of an antibody against lysosome associated membrane protein 1 (LAMP-1) measured with flow cytometry. Confirming that the assay can find compounds with desired activity, treating cells with a phorbol ester restores exocytosis. The assay behaves well in 96-well format and we screened a collection of compounds expected to have effects on epigenetic regulatory proteins. Compounds in this collection affected lytic granule exocytosis after 24-hour treatment, but none prevented cAMP from suppressing lytic granule exocytosis. We used a fully automated 384-well version of the assay to screen the Prestwick Compound Library but obtained no confirmed hits. Analyzing this assay's performance reveals two points of interest. First, cytometry offers multiple ways to quantify signals. Z’ was higher using percent positive cells than mean fluorescence because the relationship between the two measures saturates, but using percent positive could make it harder to find hits in some assays. Second, variance was higher in positive controls than in negative controls in this assay, which degrades assay performance less than if variance was higher in negative controls.

【 授权许可】

Unknown