Evidence map›Paper›PMID 39252446›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Dynamic Brain Lipid Profiles Modulate Microglial Lipid Droplet Accumulation and Inflammation Under Ischemic Conditions in Mice.

Wei Wei, Seyed Siyawasch Justus Lattau, Wenqiang Xin, Yongli Pan, Lars Tatenhorst, Lin Zhang, Irina Graf, Yaoyun Kuang, Xuan Zheng, Zhongnan Hao and 12 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing 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

43 citing papers in PubMed.

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  4. Cholesterol Drives IFITM3CNS neuroscience & therapeutics · 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

22 authors.

Wei WeiDepartment of Neurology, University Medicine Göttingen (UMG), University of Göttingen, 37075, Göttingen, Germany.
Seyed Siyawasch Justus LattauDepartment of Neurology, University Medicine Göttingen (UMG), University of Göttingen, 37075, Göttingen, Germany.ORCID 0000-0002-1595-3408
Wenqiang XinDepartment of Neurology, University Medicine Göttingen (UMG), University of Göttingen, 37075, Göttingen, Germany.
Yongli PanDepartment of Neurology, University Medicine Göttingen (UMG), University of Göttingen, 37075, Göttingen, Germany.
Lars TatenhorstDepartment of Neurology, University Medicine Göttingen (UMG), University of Göttingen, 37075, Göttingen, Germany.
Lin ZhangDepartment of Neurology, University Medicine Göttingen (UMG), University of Göttingen, 37075, Göttingen, Germany.
Irina GrafDepartment of Neurology, University Medicine Göttingen (UMG), University of Göttingen, 37075, Göttingen, Germany.
Yaoyun KuangDepartment of Neurology, University Medicine Göttingen (UMG), University of Göttingen, 37075, Göttingen, Germany.
Xuan ZhengDepartment of Neurology, University Medicine Göttingen (UMG), University of Göttingen, 37075, Göttingen, Germany.
Zhongnan HaoDepartment of Neurology, University Medicine Göttingen (UMG), University of Göttingen, 37075, Göttingen, Germany.
Aurel Popa-WagnerDepartment of Neurology, University Hospital Essen, University of Duisburg-Essen, 45147, Essen, Germany.
Stefan T GernerDepartment of Neurology, University of Giessen Medical School, 35392, Giessen, Germany.
Sabine HuberDepartment of Neurology, University of Giessen Medical School, 35392, Giessen, Germany.
Manuel NietertDepartment of Medical Bioinformatics, UMG, University of Göttingen, 37075, Göttingen, Germany.
Christian KloseLipotype GmbH, 01307, Dresden, Germany.
Ertugrul KilicDepartment of Physiology, Faculty of Medicine, Istanbul Medeniyet University, Istanbul, 34720, Turkey.
Dirk M HermannDepartment of Neurology, University Hospital Essen, University of Duisburg-Essen, 45147, Essen, Germany.
Mathias BährDepartment of Neurology, University Medicine Göttingen (UMG), University of Göttingen, 37075, Göttingen, Germany.
Hagen B HuttnerDepartment of Neurology, University of Giessen Medical School, 35392, Giessen, Germany.
Hua LiuDepartment of Neurology, The Affiliated Hospital of Southwest Jiaotong University & The Third People's Hospital of Chengdu, Chengdu, Sichuan, 610031, China.
Dirk FitznerDepartment of Neurology, University Medicine Göttingen (UMG), University of Göttingen, 37075, Göttingen, Germany.
Thorsten R DoeppnerDepartment of Neurology, University Medicine Göttingen (UMG), University of Göttingen, 37075, Göttingen, Germany.ORCID 0000-0002-1222-9211

Funding

China Scholarship Council 202008080082Deutsche Forschungsgemeinschaft TRR/SFB 274European Stroke Research Foundation
6 · The paper itself

Abstract

Microglia are critically involved in post-stroke inflammation affecting neurological outcomes. Lipid droplet (LD) accumulation in microglia results in a dysfunctional and pro-inflammatory state in the aged brain and worsens the outcome of neuroinflammatory and neurodegenerative diseases. However, the role of LD-rich microglia (LDRM) under stroke conditions is unknown. Using in vitro and in vivo stroke models, herein accumulation patterns of microglial LD and their corresponding microglial inflammatory signaling cascades are studied. Interactions between temporal and spatial dynamics of lipid profiles and microglial phenotypes in different post-stroke brain regions are found. Hence, microglia display enhanced levels of LD accumulation and elevated perilipin 2 (PLIN2) expression patterns when exposed to hypoxia or stroke. Such LDRM exhibit high levels of TNF-α, IL-6, and IL-1β as well as a pro-inflammatory phenotype and differentially expressed lipid metabolism-related genes. These post-ischemic alterations result in distinct lipid profiles with spatial and temporal dynamics, especially with regard to cholesteryl ester and triacylglycerol levels, further exacerbating post-ischemic inflammation. The present study sheds new light on the dynamic changes of brain lipid profiles and aggregation patterns of LD in microglia exposed to ischemia, demonstrating a mutual mechanism between microglial phenotype and function, which contributes to progression of brain injury.

Indexed as

BrainDisease Models, AnimalInflammationLipid DropletsMicrogliaAnimalsBrain IschemiaLipid MetabolismMaleMiceMice, Inbred C57BLStrokecholesterol metabolismischemic strokelipid dropletslipid metabolismlipidomicsmicroglianeuroinflammation

Identifiers

PMID39252446
PMCPMC11538718

What OpenQuestion holds

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Registered trials

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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.