Evidence map›Paper›PMID 32302149›Full record

ArticleJournal of proteome research2020

Quantitative Proteomics Reveals Docosahexaenoic Acid-Mediated Neuroprotective Effects in Lipopolysaccharide-Stimulated Microglial Cells.

Bo Yang, Runting Li, Pei N Liu, Xue Geng, Brian P Mooney, Chen Chen, Jianlin Cheng, Kevin L Fritsche, David Q Beversdorf, James C Lee and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of proteome research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. 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

12 authors at 2 institutions in 1 country.

Bo YangDepartment of Chemistry, University of Missouri, Columbia 65211, Missouri, United States.
Runting LiBiochemistry Department, University of Missouri, Columbia 65211, Missouri, United States.
Pei N LiuCharles W. Gehrke Proteomics Center, University of Missouri, Columbia 65211, Missouri, United States.
Xue GengDepartment of Bioengineering, University of Illinois at Chicago, Chicago 60612, Illinois, United States.
Brian P MooneyBiochemistry Department, University of Missouri, Columbia 65211, Missouri, United States.
Chen ChenDepartment of Electrical Engineering and Computer Science, University of Missouri, Columbia 65211, Missouri, United States.
Jianlin ChengDepartment of Electrical Engineering and Computer Science, University of Missouri, Columbia 65211, Missouri, United States.
Kevin L FritscheDepartment of Nutrition and Exercise Physiology, University of Missouri, Columbia 65211, Missouri, United States.
David Q BeversdorfDepartments of Radiology, Neurology and Psychological Sciences, and the Thompson Center, University of Missouri, Columbia 65211, Missouri, United States.
James C LeeDepartment of Bioengineering, University of Illinois at Chicago, Chicago 60612, Illinois, United States.ORCID 0000-0002-7173-4875
Grace Y SunBiochemistry Department, University of Missouri, Columbia 65211, Missouri, United States.
C Michael GreenliefDepartment of Chemistry, University of Missouri, Columbia 65211, Missouri, United States.ORCID 0000-0001-6420-7375
University of Missouri · USUniversity of Illinois Chicago · US

Funding

Roles of Tau Oligomers in Alzheimer's VasculopathyR01AG044404 · NIA · UNIVERSITY OF MISSOURI-COLUMBIA · PI LEE, JAMES C · 2014 to 2024
$3.5M
NIA NIH HHS R01 AG044404
6 · The paper itself

Abstract

The high levels of docosahexaenoic acid (DHA) in cell membranes within the brain have led to a number of studies exploring its function. These studies have shown that DHA can reduce inflammatory responses in microglial cells. However, the method of action is poorly understood. Here, we report the effects of DHA on microglial cells stimulated with lipopolysaccharides (LPSs). Data were acquired using the parallel accumulation serial fragmentation method in a hybrid trapped ion mobility-quadrupole time-of-flight mass spectrometer. Over 2800 proteins are identified using label-free quantitative proteomics. Cells exposed to LPSs and/or DHA resulted in changes in cell morphology and expression of 49 proteins with differential abundance (greater than 1.5-fold change). The data provide details about pathways that are influenced in this system including the nuclear factor κ-light-chain-enhancer of the activated B cells (NF-κB) pathway. Western blots and enzyme-linked immunosorbent assay studies are used to help confirm the proteomic results. The MS data are available at ProteomeXchange.

Indexed as

LipopolysaccharidesNeuroprotective AgentsCytokinesDocosahexaenoic AcidsMicrogliaNF-kappa BProteomicsCytokinesDocosahexaenoic AcidsLipopolysaccharidesNeuroprotective AgentsNF-kappa Bdocosahexaenoic acidion mobilitylabel-free quantificationlipopolysaccharidemicrogliatime-of-flightTIMS

Identifiers

PMID32302149
PMCPMC7282485
OpenAlexW3016673405

What Socratic 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 Socratic graph.