Evidence map›Paper›PMID 31522382›Full record

ArticleMolecular neurobiology2020

Predicting Reactive Astrogliosis Propagation by Bayesian Computational Modeling: the Repeater Stations Model.

Jerónimo Auzmendi, Luciano Moffatt, Alberto Javier Ramos

Abstract read
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In one paragraph

Article in Molecular neurobiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Intrathecal Administration of an Anti-nociceptive Non-CpG Oligodeoxynucleotide Reduces Glial Activation and Central Sensitization.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2021
    Article
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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

3 authors at 1 institution in 1 country.

Jerónimo AuzmendiLaboratorio de Neuropatología Molecular, Instituto de Biología Celular y Neurociencia "Prof. E. De Robertis" UBA-CONICET, Facultad de Medicina, Universidad de Buenos Aires, Paraguay 2155 3er piso (1121), Buenos Aires, Argentina.
Luciano MoffattInstituto de Química Física de los Materiales, Medio Ambiente y Energía, Facultad de Ciencias Exactas y Naturales, UBA-CONICET, Universidad de Buenos Aires, Ricardo Guiraldes 2160 (1428), Buenos Aires, Argentina. lmoffatt@qi.fcen.uba.ar.
Alberto Javier RamosLaboratorio de Neuropatología Molecular, Instituto de Biología Celular y Neurociencia "Prof. E. De Robertis" UBA-CONICET, Facultad de Medicina, Universidad de Buenos Aires, Paraguay 2155 3er piso (1121), Buenos Aires, Argentina. jramos@fmed.uba.ar.ORCID http://orcid.org/0000-0003-4009-6337
Consejo Nacional de Investigaciones Científicas y Técnicas · AR

Funding

Consejo Nacional de Investigaciones Científicas y Técnicas PIP 0479Fondo para la Investigación Científica y Tecnológica PICT 2015-1451Fondo para la Investigación Científica y Tecnológica PICT 2017-2203Secretaria de Ciencia y Tecnica, Universidad de Buenos Aires 20020110100141
6 · The paper itself

Abstract

Reactive astrogliosis occurs upon focal brain injury and in neurodegenerative diseases. The mechanisms that propagate reactive astrogliosis to distal parts of the brain, in a rapid wave that activates astrocytes and other cell types along the way, are not completely understood. It is proposed that damage-associated molecular patterns (DAMP) released by necrotic cells from the injury core have a major role in the reactive astrogliosis initiation but whether they also participate in reactive astrogliosis propagation remains to be determined. We here developed a Bayesian computational model to define the most probable model for reactive astrogliosis propagation. Starting with experimental data from GFAP-immunostained reactive astrocytes, we defined five types of astrocytes based on morphometrical cues and registered the position of each reactive astrocyte cell type in the hemisphere ipsilateral to the injured site after 3 and 7 days post-ischemia. We developed equations for the changes in DAMP concentration (due to diffusion, binding to receptors or degradation), soluble mediators secretion, and for the evolution reactive astrogliosis. We tested four predefined models based on abovementioned previous hypothesis and modifications to it. Our results showed that DAMP diffusion alone has not justified the reactive astrogliosis propagation as previously assumed. Only two models succeeded in accurately reproducing the experimentally measured data and they highlighted the role of microglia and the glial secretion of soluble mediators to sustain the reactive signal and activating neighboring astrocytes. Thus, our in silico analysis proposes that glial cells behave as repeater stations of the injury signal in order to propagate reactive astrogliosis.

Indexed as

AnimalsAstrocytesBayes TheoremBrainBrain InjuriesCells, CulturedGlial Fibrillary Acidic ProteinGliosisInflammationMaleMicrogliaRats, WistarGlial Fibrillary Acidic ProteinAstrocyteBayesComputational modelingNeuroinflammationReactive gliosis

Identifiers

PMID31522382
OpenAlexW2972663745

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.