Evidence map›Paper›PMID 39218899›Full record

ArticleJournal of neuroinflammation2024

Suppression of the JAK/STAT pathway inhibits neuroinflammation in the line 61-PFF mouse model of Parkinson's disease.

Huixian Hong, Yong Wang, Marissa Menard, Jessica A Buckley, Lianna Zhou, Laura Volpicelli-Daley, David G Standaert, Hongwei Qin, Etty N Benveniste

Abstract read
In one paragraph

Article in Journal of neuroinflammation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
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

21 citing papers in PubMed.

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  20. Energy metabolism in health and diseases.Signal transduction and targeted therapy · 2025
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Huixian Hong *Department of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, 1918 University Boulevard, MCLM 907, Birmingham, AL, 35294, USA.
Yong Wang *Department of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, 1918 University Boulevard, MCLM 907, Birmingham, AL, 35294, USA.
Marissa Menard *Department of Neurology, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
Jessica A BuckleyDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, 1918 University Boulevard, MCLM 907, Birmingham, AL, 35294, USA.
Lianna ZhouDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, 1918 University Boulevard, MCLM 907, Birmingham, AL, 35294, USA.
Laura Volpicelli-DaleyDepartment of Neurology, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
David G StandaertDepartment of Neurology, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
Hongwei QinDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, 1918 University Boulevard, MCLM 907, Birmingham, AL, 35294, USA. hqin@uab.edu.
Etty N BenvenisteDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, 1918 University Boulevard, MCLM 907, Birmingham, AL, 35294, USA. tika@uab.edu.

Funding

XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Omer Jamy · 1985 to 2026
$165.9M
Virology CoreP30AI027767 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Paul A. Goepfert · 1988 to 2026
$84.1M
Project 3: LRRK2 mediated macrophage responses in PDP50NS108675 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI STANDAERT, DAVID G. · 2018 to 2022
$9.9M
Astrocytic OSMR/JAK/STAT signaling in ADR01AG075057 · NIA · AUGUSTA UNIVERSITY · PI Hongwei Qin, Qin Wang · 2023 to 2026
$2.5M
National Institutes of Health (NIH) P50NS108675, AG075057, NIH AI027767, NIH CA013148NCI NIH HHS P30 CA013148NIAID NIH HHS P30 AI027767NIA NIH HHS R01 AG075057NINDS NIH HHS P50 NS108675
6 · The paper itself

Abstract

Parkinson's disease (PD) is characterized by neuroinflammation, progressive loss of dopaminergic neurons, and accumulation of α-synuclein (α-Syn) into insoluble aggregates called Lewy pathology. The Line 61 α-Syn mouse is an established preclinical model of PD; Thy-1 is used to promote human α-Syn expression, and features of sporadic PD develop at 9-18 months of age. To accelerate the PD phenotypes, we injected sonicated human α-Syn preformed fibrils (PFFs) into the striatum, which produced phospho-Syn (p-α-Syn) inclusions in the substantia nigra pars compacta and significantly increased MHC Class II-positive immune cells. Additionally, there was enhanced infiltration and activation of innate and adaptive immune cells in the midbrain. We then used this new model, Line 61-PFF, to investigate the effect of inhibiting the JAK/STAT signaling pathway, which is critical for regulation of innate and adaptive immune responses. After administration of the JAK1/2 inhibitor AZD1480, immunofluorescence staining showed a significant decrease in p-α-Syn inclusions and MHC Class II expression. Flow cytometry showed reduced infiltration of CD4

Indexed as

alpha-SynucleinDisease Models, AnimalNeuroinflammatory DiseasesParkinson DiseaseSignal TransductionSTAT Transcription FactorsAnimalsHumansJanus KinasesMiceMice, Inbred C57BLMice, TransgenicParkinsonian DisordersPyrimidinesalpha-SynucleinJanus KinasesPyrimidinesSTAT Transcription FactorsAZD1480JAK/STATNeuroinflammationParkinson’s diseasescRNA-Seqα-Synuclein

Identifiers

PMID39218899
PMCPMC11368013

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.