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Research Articles

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

ORCID Icon, ORCID Icon, ORCID Icon & ORCID Icon
Pages 666-676 | Received 23 Oct 2022, Accepted 01 Jan 2023, Published online: 11 Jan 2023
 

Abstract

Hydrogen peroxide (H2O2) is a ubiquitous oxidant produced in a regulated manner by various enzymes in mammalian cells. H2O2 reversibly oxidizes thiol groups of cysteine residues to mediate intracellular signaling. While examples of H2O2-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 H2O2 was investigated to determine global effects on gene expression. With a low H2O2 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 H2O2 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 H2O2, which, along with further studies, will lead to new insights into the specific pathways that are activated in response to endogenous production of H2O2, and the molecular mechanisms of H2O2 signaling.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Data availability statement

The RNA-Seq data have been deposited in NCBI’s Gene Expression Omnibus [1] and are accessible through GEO Series accession number GSE206509 (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE206509).

Additional information

Funding

This work was supported by an University of Otago Doctoral scholarship and a Freemasons NZ postgraduate scholarship to MFT, and a Royal Society of New Zealand Marsden Fund Grant [17-UOO-086] to MBH.