Evidence map›Paper›PMID 27080543›Full record

ArticleMolecular neurobiology2017

Phosphoinositides: Two-Path Signaling in Neuronal Response to Oligomeric Amyloid β Peptide.

Romina María Uranga, Natalia Paola Alza, Melisa Ailén Conde, Silvia Susana Antollini, Gabriela Alejandra Salvador

Abstract read
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In one paragraph

Article in Molecular neurobiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Oxidative medicine and cellular longevity · 2023
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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

5 authors at 4 institutions in 1 country.

Romina María UrangaInstituto de Investigaciones Bioquímicas de Bahía Blanca, La Carrindanga Km 7, 8000, Bahía Blanca, Buenos Aires, Argentina.
Natalia Paola AlzaInstituto de Investigaciones Bioquímicas de Bahía Blanca, La Carrindanga Km 7, 8000, Bahía Blanca, Buenos Aires, Argentina.
Melisa Ailén CondeInstituto de Investigaciones Bioquímicas de Bahía Blanca, La Carrindanga Km 7, 8000, Bahía Blanca, Buenos Aires, Argentina.
Silvia Susana AntolliniInstituto de Investigaciones Bioquímicas de Bahía Blanca, La Carrindanga Km 7, 8000, Bahía Blanca, Buenos Aires, Argentina.
Gabriela Alejandra SalvadorInstituto de Investigaciones Bioquímicas de Bahía Blanca, La Carrindanga Km 7, 8000, Bahía Blanca, Buenos Aires, Argentina. salvador@criba.edu.ar.
Instituto de Investigaciones Bioquímicas de Bahía Blanca, CONICET-UNSCentro Científico Tecnológico - Bahía Blanca · ARConsejo Nacional de Investigaciones Científicas y Técnicas · ARUniversidad Nacional del Sur · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have previously demonstrated that oligomeric amyloid β peptide (oAβ) together with iron overload generates synaptic injury and activation of several signaling cascades. In this work, we characterized hippocampal neuronal response to oAβ. HT22 neurons exposed to 500 nM oAβ showed neither increased lipid peroxidation nor altered mitochondrial function. In addition, biophysical studies showed that oAβ did not perturb the lipid order of the membrane. Interestingly, although no neuronal damage could be demonstrated, oAβ was found to trigger bifurcated phosphoinositide-dependent signaling in the neuron, on one hand, the phosphorylation of insulin receptor, the phosphatidylinositol 3-kinase (PI3K)-dependent activation of Akt, its translocation to the nucleus and the concomitant phosphorylation, inactivation, and nuclear exclusion of the transcription factor Forkhead Box O3a (FoxO3a), and on the other, phosphoinositide-phospholipase C (PI-PLC)-dependent extracellular signal-regulated kinase 1/2 (ERK1/2) activation. Pharmacological manipulation of the signaling cascades was used in order to better characterize the role of oAβ-activated signals, and mitochondrial function was determined as a measure of neuronal viability. The inhibition of PI3K, PI-PLC, and general phosphoinositide metabolism impaired neuronal mitochondrial function. Furthermore, increased oAβ-induced cell death was observed in the presence of phosphoinositide metabolism inhibition. Our results allow us to conclude that oAβ triggers the activation of phosphoinositide-dependent signaling, which results in the subsequent activation of neuroprotective mechanisms that could be involved in the determination of neuronal fate.

Indexed as

Protein MultimerizationSignal TransductionAmyloid beta-PeptidesAnimalsCell LineExtracellular Signal-Regulated MAP KinasesForkhead Box Protein O3HumansMiceNeuronsPhosphatidylinositol 3-KinasesPhosphatidylinositolsProtein AggregatesProto-Oncogene Proteins c-aktRatsReceptor, InsulinAmyloid beta-PeptidesExtracellular Signal-Regulated MAP KinasesForkhead Box Protein O3FoxO3 protein, mousePhosphatidylinositol 3-KinasesPhosphatidylinositolsProtein AggregatesProto-Oncogene Proteins c-aktReceptor, InsulinAmyloid β peptideERK1/2FoxOPhosphoinositidesPI3KPI-PLC

Identifiers

PMID27080543
OpenAlexW2338749379

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.