Evidence map›Paper›PMID 40066444›Full record

ArticleFrontiers in immunology2025

The changes of NLRs family members in the brain of AD mouse model and AD patients.

Zehan Li, Yanling He, Jingdan Zhang, Jing Yang, Jinbo Cheng, Xuewu Zhang

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

6 authors.

Zehan LiCollege of Medicine, Yanbian University, Yanji, China.
Yanling HeSchool of Basic Medical Sciences, Anhui Medical University, Hefei, China.
Jingdan ZhangThe Brain Science Center, Beijing Institute of Basic Medical Sciences, Beijing, China.
Jing YangKey Laboratory of Neurology (Hebei Medical University), Ministry of Education, Shijiazhuang, China.
Jinbo ChengSchool of Basic Medical Sciences, Anhui Medical University, Hefei, China.
Xuewu ZhangCollege of Medicine, Yanbian University, Yanji, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Alzheimer's disease (AD), a prevalent neurodegenerative disease, is primarily characterized by progressive neuron loss and memory impairment. NOD-like receptors (NLRs) are crucial for immune regulation and maintaining cellular homeostasis. Recently, NLRs have been identified as important contributors to neuroinflammation, thus presenting a potential approach for reducing inflammation and slowing AD progression. Methods: We use quantitative RT-PCR to detect levels of NLR family members in AD mouse model. Additionally, we use immunofluorescence to detect NLRP3 expressions in microglia surrounding Aβ plaques in AD mouse model and human AD patients. Results: In this study, we examined the expression of NLR family members in the human AD database, and found increased levels of CIITA, NOD1, NLRC5, NLRP1, NLRP3, NLRP7, NLRP10, NLRP12, and NLRP13 in hippocampus tissue in patients with AD, along with increased levels of NOD1, NLRC5, NLRX1, NLRP3, and NLRP7 levels in frontal cortex tissue. Furthermore, through detecting their levels in AD mouse model, we found that NLRP3 levels were significantly increased. Additionally, we found that NLRP3 expressions were mainly elevated in microglia surrounding Aβ plaques in AD mouse model and human AD patients. Discussion: These findings highlight the potential important role of NLRP3 in AD pathology, offering new therapeutic targets and interventions.

Indexed as

Alzheimer DiseaseBrainNLR ProteinsAgedAnimalsDisease Models, AnimalFemaleHumansMaleMiceMice, Inbred C57BLMice, TransgenicMicrogliaNLR Family, Pyrin Domain-Containing 3 ProteinNLR Family, Pyrin Domain-Containing 3 ProteinNLR ProteinsAlzheimer’s diseaseAβ plaquesmicrogliaNLRP3NLRs

Identifiers

PMID40066444
PMCPMC11891040

What OpenQuestion holds

Textmetadata
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.