Evidence map›Paper›PMID 26037803›Full record

ArticleNeuroscience2015

Astrocytes regulate α-secretase-cleaved soluble amyloid precursor protein secretion in neuronal cells: Involvement of group IIA secretory phospholipase A2.

X Yang, W Sheng, D M Ridgley, M A Haidekker, G Y Sun, J C Lee

Open access · greenAbstract read
In one paragraph

Article in Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Review
  3. Rat Group IIA Secreted Phospholipase AInternational journal of molecular sciences · 2022
    Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. APP as a Protective Factor in Acute Neuronal Insults.Frontiers in molecular neuroscience · 2017
    Review
  9. 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 at 3 institutions in 1 country.

X YangHope Center for Neurological Disorders and Department of Neurology, Washington University School of Medicine, St. Louis, MO 63110, United States.
W ShengDepartment of Biochemistry, University of Missouri, Columbia, MO 65211, United States.
D M RidgleyDepartment of Bioengineering, University of Missouri, Columbia, MO 65211, United States.
M A HaidekkerCollege of Engineering, Driftmier Engineering Center, University of Georgia, Athens, GA 30602, United States.
G Y SunDepartment of Biochemistry, University of Missouri, Columbia, MO 65211, United States.
J C LeeDepartment of Bioengineering, University of Missouri, Columbia, MO 65211, United States; Department of Bioengineering, University of Illinois at Chicago, Chicago, IL 60607, United States. Electronic address: leejam@missouri.edu.
University of Missouri · USHope Center for Neurological Disorders · USUniversity of Georgia · US

Funding

PATHOGENESIS OF PHOSPHOLIPASES A2 IN ADP01AG018357 · NIA · UNIVERSITY OF MISSOURI-COLUMBIA · PI SUN, GRACE Y · 2001 to 2012
$10.4M
Roles of Tau Oligomers in Alzheimer's VasculopathyR01AG044404 · NIA · UNIVERSITY OF MISSOURI-COLUMBIA · PI LEE, JAMES C · 2014 to 2024
$3.5M
Effects of oxidative stress on glial cell membranesR21NS052385 · NINDS · UNIVERSITY OF MISSOURI-COLUMBIA · PI LEE, JAMES C · 2007 to 2008
$344k
Amyloid-B peptide on endothelial adhesion and its related cellular pathwaysR21AG032579 · NIA · UNIVERSITY OF MISSOURI-COLUMBIA · PI LEE, JAMES C · 2009 to 2010
$340k
NIA NIH HHS 1 R01 AG044404NIA NIH HHS 5 R21 AG032579NIA NIH HHS P01 AG018357NIA NIH HHS R01 AG044404NIA NIH HHS R21 AG032579NINDS NIH HHS 1 R21 NS052385NINDS NIH HHS R21 NS052385
6 · The paper itself

Abstract

Astrocytes are major supportive cells in brains with important functions including providing nutrients and regulating neuronal activities. In this study, we demonstrated that astrocytes regulate amyloid precursor protein (APP) processing in neuronal cells through secretion of group IIA secretory phospholipase A2 (sPLA2-IIA). When astrocytic cells (DITNC) were mildly stimulated with the pro-inflammatory cytokines, such as TNF α and IL-1β, sPLA2-IIA was secreted into the medium. When conditioned medium containing sPLA2-IIA was applied to human neuroblastoma (SH-SY5Y) cells, there was an increase in both cell membrane fluidity and secretion of α-secretase-cleaved soluble amyloid precursor protein (sAPPα). These changes were abrogated by KH064, a selective inhibitor of sPLA2-IIA. In addition, exposing SH-SY5Y cells to recombinant human sPLA2-IIA also increased membrane fluidity, accumulation of APP at the cell surface, and secretion of sAPPα, but without altering total expressions of APP, α-secretases and β-site APP cleaving enzyme (BACE1). Taken together, our results provide novel information regarding a functional role of sPLA2-IIA in astrocytes for regulating APP processing in neuronal cells.

Indexed as

Amyloid beta-PeptidesAmyloid Precursor Protein SecretasesAstrocytesBlotting, WesternCell Line, TumorCell MembraneCell SurvivalCulture Media, ConditionedFluorescent Antibody TechniqueGroup II Phospholipases A2HumansMembrane FluidityMicroscopy, FluorescenceNeuronsPeptide FragmentsAmyloid beta-Peptidesamyloid beta-protein (1-42)Amyloid Precursor Protein SecretasesCulture Media, ConditionedGroup II Phospholipases A2Peptide Fragmentsastrocytescytokinemembrane fluiditysAPP(α)SH-SY5YsPLA(2)-IIA

Identifiers

PMID26037803
PMCPMC4485573
OpenAlexW897544685

What OpenQuestion holds

Textmetadata
LicenceTDM
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.