RGS10 differentially modulates NFκB subunit transcription and inflammatory cytokine profiles in peritoneal macrophages

Regulator of G-protein signaling 10 (RGS10) has been shown to regulate multiple inflammatory pathways relevant to disease pathogenesis. Of particular importance is the ability of RGS10 to negatively regulate the NFkB pathway, a prominent pro-inflammatory pathway implicated in multiple inflammatory disease phenotypes. However, the exact mechanism by which RGS10 regulates NFkB is unknown. Considering that RGS10 translocates into the nucleus upon stimulation, we hypothesize that RGS10 may regulate NFKB through transcription. To determine whether RGS10 mediates NFkB transcription, we stimulated RGS10 KO and B6 peritoneal macrophages and collected cell lysate over 24 hours to assess transcript levels of NFkB and related proinflammatory cytokines. Here we found that RGS10 differentially regulates the transcription of NκKB subunits and NFκB-dependent cytokines. Further studies are warranted to understand the potential role of RGS10 in transcriptional regulation of inflammatory states.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-02-11
DOI
https://doi.org/10.64898/2026.02.09.704897
Primary Topic
NF-κB Signaling Pathways
Type
article
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0.00
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article

RGS10 differentially modulates NFκB subunit transcription and inflammatory cytokine profiles in peritoneal macrophages

C Cole, Kelly B. Menees, Noelle K. Neighbarger, Kruthika Dheeravath et al.
bioRxiv (Cold Spring Harbor Laboratory)
NF-κB Signaling Pathways
article

RGS10 differentially modulates NFκB subunit transcription and inflammatory cytokine profiles in peritoneal macrophages

C Cole, Kelly B. Menees, Noelle K. Neighbarger, Kruthika Dheeravath, Malú Gámez Tansey, Janna E Jernigan Posey
article en

Abstract

Regulator of G-protein signaling 10 (RGS10) has been shown to regulate multiple inflammatory pathways relevant to disease pathogenesis. Of particular importance is the ability of RGS10 to negatively regulate the NFkB pathway, a prominent pro-inflammatory pathway implicated in multiple inflammatory disease phenotypes. However, the exact mechanism by which RGS10 regulates NFkB is unknown. Considering that RGS10 translocates into the nucleus upon stimulation, we hypothesize that RGS10 may regulate NFKB through transcription. To determine whether RGS10 mediates NFkB transcription, we stimulated RGS10 KO and B6 peritoneal macrophages and collected cell lysate over 24 hours to assess transcript levels of NFkB and related proinflammatory cytokines. Here we found that RGS10 differentially regulates the transcription of NκKB subunits and NFκB-dependent cytokines. Further studies are warranted to understand the potential role of RGS10 in transcriptional regulation of inflammatory states.

bioRxiv (Cold Spring Harbor Laboratory)
University of Florida (US), Indiana University – Purdue University Indianapolis (US)
Good health and well-being
Openalex Percentile: Top 61%
NF-κB Signaling Pathways
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