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Insights into H2O2-induced signaling in Jurkat cells from analysis of gene expression.

Authors :
Taylor, Megan F.
Black, Michael A.
Hampton, Mark B.
Ledgerwood, Elizabeth C.
Source :
Free Radical Research; Sep/Oct2022, Vol. 56 Issue 9/10, p666-676, 11p, 2 Charts, 4 Graphs
Publication Year :
2022

Abstract

Hydrogen peroxide (H<subscript>2</subscript>O<subscript>2</subscript>) is a ubiquitous oxidant produced in a regulated manner by various enzymes in mammalian cells. H<subscript>2</subscript>O<subscript>2</subscript> reversibly oxidizes thiol groups of cysteine residues to mediate intracellular signaling. While examples of H<subscript>2</subscript>O<subscript>2-</subscript>dependent signaling have been reported, the exact molecular mechanism(s) of signaling and the pathways affected are not well understood. Here, the transcriptomic response of Jurkat T cells to H<subscript>2</subscript>O<subscript>2</subscript> was investigated to determine global effects on gene expression. With a low H<subscript>2</subscript>O<subscript>2</subscript> concentration (10 µM) that did not induce an oxidative stress response or cell death, extensive changes in gene expression occurred after 4 h (6803 differentially expressed genes). Of the genes with a greater then 2-fold change in expression, 85% were upregulated suggesting that in a physiological setting H<subscript>2</subscript>O<subscript>2</subscript> predominantly activates gene expression. Pathway analysis identified gene expression signatures associated with FOXO and NTRK signaling. These signatures were associated with an overlapping set of transcriptional regulators. Overall, our results provide a snapshot of gene expression changes in response to H<subscript>2</subscript>O<subscript>2,</subscript> which, along with further studies, will lead to new insights into the specific pathways that are activated in response to endogenous production of H<subscript>2</subscript>O<subscript>2</subscript>, and the molecular mechanisms of H<subscript>2</subscript>O<subscript>2</subscript> signaling. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10715762
Volume :
56
Issue :
9/10
Database :
Complementary Index
Journal :
Free Radical Research
Publication Type :
Academic Journal
Accession number :
161688559
Full Text :
https://doi.org/10.1080/10715762.2023.2165073