Evidence map›Paper›PMID 36594555›Full record

ArticleJournal of cell science2023

Regulation of macrophage IFNγ-stimulated gene expression by the transcriptional coregulator CITED1.

Aarthi Subramani, Maria E L Hite, Sarah Garcia, Jack Maxwell, Hursha Kondee, Grace E Millican, Erin E McClelland, Rebecca L Seipelt-Thiemann, David E Nelson

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cell science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Cited2 is a key regulator of placental development and plasticity.BioEssays : news and reviews in molecular, cellular and developmental biology · 2024
    Review
  10. Article
  11. Review
  12. Roles and signaling pathways of CITED1 in tumors: overview and novel insights.The Journal of international medical research · 2024
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Aarthi SubramaniDepartment of Biology, Middle Tennessee State University, Murfreesboro, TN 37132, USA.ORCID 0000-0003-1094-9554
Maria E L HiteDepartment of Biology, Middle Tennessee State University, Murfreesboro, TN 37132, USA.
Sarah GarciaDepartment of Biology, Middle Tennessee State University, Murfreesboro, TN 37132, USA.
Jack MaxwellDepartment of Biology, Middle Tennessee State University, Murfreesboro, TN 37132, USA.
Hursha KondeeDepartment of Biology, Middle Tennessee State University, Murfreesboro, TN 37132, USA.
Grace E MillicanDepartment of Biology, Middle Tennessee State University, Murfreesboro, TN 37132, USA.
Erin E McClellandCollege of Osteopathic Medicine, Marian University, Indianapolis, IN 46222, USA.
Rebecca L Seipelt-ThiemannDepartment of Biology, Middle Tennessee State University, Murfreesboro, TN 37132, USA.ORCID 0000-0001-5265-7897
David E NelsonDepartment of Biology, Middle Tennessee State University, Murfreesboro, TN 37132, USA.ORCID 0000-0002-5034-0885
Middle Tennessee State University · USMarian University - Indiana · US

Funding

Modulation of Macrophage Polarization by a Facultative Intracellular PathogenR15AI135826 · NIAID · MIDDLE TENNESSEE STATE UNIVERSITY · PI NELSON, DAVID EDWARD · 2018 to 2018
$392k
NIAID NIH HHS R15 AI135826NIH HHS 1R15AI135826-01
6 · The paper itself

Abstract

Macrophages serve as a first line of defense against microbial pathogens. Exposure to interferon-γ (IFNγ) increases interferon-stimulated gene (ISG) expression in these cells, resulting in enhanced antimicrobial and proinflammatory activity. Although this response must be sufficiently vigorous to ensure the successful clearance of pathogens, it must also be carefully regulated to prevent tissue damage. This is controlled in part by CBP/p300-interacting transactivator with glutamic acid/aspartic acid-rich carboxyl-terminal domain 2 (CITED2), a transcriptional coregulator that limits ISG expression by inhibiting STAT1 and IRF1. Here, we show that the closely related Cited1 is an ISG, which is expressed in a STAT1-dependent manner, and that IFNγ stimulates the nuclear accumulation of CITED1 protein. In contrast to CITED2, ectopic CITED1 enhanced the expression of a subset of ISGs, including Ccl2, Ifit3b, Isg15 and Oas2. This effect was reversed in a Cited1-null cell line produced by CRISPR-based genomic editing. Collectively, these data show that CITED1 maintains proinflammatory gene expression during periods of prolonged IFNγ exposure and suggest that there is an antagonistic relationship between CITED proteins in the regulation of macrophage inflammatory function. This article has an associated First Person interview with the first author of the paper.

Indexed as

Interferon-gammaNuclear ProteinsGene ExpressionGene Expression RegulationHumansMacrophagesRepressor ProteinsSTAT1 Transcription FactorTrans-ActivatorsCITED2 protein, humanInterferon-gammaNuclear ProteinsRepressor ProteinsSTAT1 Transcription FactorTrans-ActivatorsCITED1Interferon-γMacrophageMacrophage polarizationSTAT1

Identifiers

PMID36594555
PMCPMC10112972
OpenAlexW4313462831

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.