Evidence map›Paper›PMID 36379959›Full record

ArticleNature communications2022

Interruption of post-Golgi STING trafficking activates tonic interferon signaling.

Xintao Tu, Ting-Ting Chu, Devon Jeltema, Kennady Abbott, Kun Yang, Cong Xing, Jie Han, Nicole Dobbs, Nan Yan

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.3field-weighted citation impact, top 4% 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

44 citing papers in PubMed, 55 citations in OpenAlex.

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  8. PARP7 protects the lung epithelial barrier from diverse environmental threats.Proceedings of the National Academy of Sciences of the United States of America · 2026
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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 1 institution in 1 country.

Xintao TuDepartment of Immunology, UT Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0001-8789-5297
Ting-Ting ChuDepartment of Immunology, UT Southwestern Medical Center, Dallas, TX, USA.
Devon JeltemaDepartment of Immunology, UT Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0002-5338-3477
Kennady AbbottDepartment of Immunology, UT Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0003-3874-1691
Kun YangDepartment of Immunology, UT Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0002-2011-7084
Cong XingDepartment of Immunology, UT Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0001-9641-335X
Jie HanDepartment of Immunology, UT Southwestern Medical Center, Dallas, TX, USA.
Nicole DobbsDepartment of Immunology, UT Southwestern Medical Center, Dallas, TX, USA.
Nan YanDepartment of Immunology, UT Southwestern Medical Center, Dallas, TX, USA. nan.yan@utsouthwestern.edu.ORCID 0000-0002-0637-3989
Southwestern Medical Center · US

Funding

UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MELANIE H. COBB · 2010 to 2026
$53.7M
INTEGRATIVE IMMUNOLOGY TRAINING PROGRAMT32AI005284 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI Nan Yan · 2003 to 2026
$7.4M
Mechanism of STING-mediated Neuropathology in Niemann-Pick DiseaseR01NS122825 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI YAN, NAN · 2021 to 2025
$2.4M
The Mitochondrion-STING Axis in An Early Childhood Onset Neurodegenerative DiseaseR01NS117424 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI YAN, NAN · 2021 to 2025
$2.3M
Sting Trafficking and Signaling Beyond InterferonR01AI151708 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI YAN, NAN · 2020 to 2023
$2.1M
Spinning Disk Confocal for UT SouthwesternS10OD028630 · OD · UT SOUTHWESTERN MEDICAL CENTER · PI LUBY-PHELPS, KATHERINE J · 2020 to 2020
$600k
STING Signaling in Health and DiseaseR56AI151708 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI YAN, NAN · 2024 to 2024
$339k
NCI NIH HHS P30 CA142543NIAID NIH HHS R01 AI151708NIAID NIH HHS R56 AI151708NIAID NIH HHS T32 AI005284NIH HHS S10 OD028630NINDS NIH HHS R01 NS117424NINDS NIH HHS R01 NS122825
6 · The paper itself

Abstract

Activation of the cGAS-STING pathway is traditionally considered a "trigger-release" mechanism where detection of microbial DNA or cyclic di-nucleotides sets off the type I interferon response. Whether this pathway can be activated without pathogenic ligand exposure is less well understood. Here we show that loss of Golgi-to-lysosome STING cofactors, but not ER-to-Golgi cofactors, selectively activates tonic interferon signalling. Impairment of post-Golgi trafficking extends STING Golgi-dwell time, resulting in elevated immune signalling and protection against infection. Mechanistically, trans-Golgi coiled coil protein GCC2 and several RAB GTPases act as key regulators of STING post-Golgi trafficking. Genomic deletion of these factors potently activates cGAS-STING signalling without instigating any pathogenic trigger for cGAS. Gcc2

Indexed as

Interferon Type IMembrane ProteinsAnimalsGolgi ApparatusImmunity, InnateMiceNucleotides, CyclicNucleotidyltransferasesInterferon Type IMembrane ProteinsNucleotides, CyclicNucleotidyltransferases

Identifiers

PMID36379959
PMCPMC9666523
OpenAlexW4309190979

What OpenQuestion holds

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LicenceCC BY
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.