Evidence map›Paper›PMID 32623553›Full record

ArticleMetabolic brain disease2020

Evidence for inflammasome activation in the brain of mucopolysaccharidosis type II mice.

A S Azambuja, L N Pimentel-Vera, E A Gonzalez, E Poletto, C V Pinheiro, U Matte, R Giugliani, Guilherme Baldo

Abstract read
PubMed Publisher
In one paragraph

Article in Metabolic brain disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Genome Editing Tools for Lysosomal Storage Disorders.Advances in experimental medicine and biology · 2023
    Article
  7. Article
  8. Article
  9. Innate Immunity in Mucopolysaccharide Diseases.International journal of molecular sciences · 2022
    Review
  10. Review
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

8 authors at 2 institutions in 1 country.

A S AzambujaPrograma de Pós-Graduação em Ciências Biológicas: Fisiologia, UFRGS, Porto Alegre, Brazil.
L N Pimentel-VeraCentro de Terapia Gênica-HCPA, Hospital de Clínicas de Porto Alegre, Ramiro Barcelos, 2350, Porto Alegre, RS, 90035-903, Brazil.
E A GonzalezCentro de Terapia Gênica-HCPA, Hospital de Clínicas de Porto Alegre, Ramiro Barcelos, 2350, Porto Alegre, RS, 90035-903, Brazil.
E PolettoCentro de Terapia Gênica-HCPA, Hospital de Clínicas de Porto Alegre, Ramiro Barcelos, 2350, Porto Alegre, RS, 90035-903, Brazil.
C V PinheiroCentro de Terapia Gênica-HCPA, Hospital de Clínicas de Porto Alegre, Ramiro Barcelos, 2350, Porto Alegre, RS, 90035-903, Brazil.
U MatteCentro de Terapia Gênica-HCPA, Hospital de Clínicas de Porto Alegre, Ramiro Barcelos, 2350, Porto Alegre, RS, 90035-903, Brazil.
R GiuglianiCentro de Terapia Gênica-HCPA, Hospital de Clínicas de Porto Alegre, Ramiro Barcelos, 2350, Porto Alegre, RS, 90035-903, Brazil.
Guilherme BaldoPrograma de Pós-Graduação em Ciências Biológicas: Fisiologia, UFRGS, Porto Alegre, Brazil. gbaldo@hcpa.edu.br.ORCID http://orcid.org/0000-0003-1598-5861
Universidade Federal do Rio Grande do Sul · BRHospital de Clínicas de Porto Alegre · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hunter syndrome or mucopolysaccharidosis type II (MPS II) is an X-linked recessive disease caused by the deficiency of iduronate 2-sulfatase (IDS), leading to storage of undegraded heparan and dermatan sulfate. Patients with the severe form present neurological abnormalities, but the mechanisms of such alterations are unknown. Here, we hypothesized that the undegraded substances found in this disease could be recognized as damage-associated molecular patterns (DAMPS), leading to activation of the inflammasome. Brains from 2 and 5 months normal and MPS II mice were studied. We observed an increase in cathepsin B activity in the brain tissue and leakage of this enzyme from the lysosome to the cytoplasm in a MPS II neuronal cell line, which is a known activator of the inflammasome. Furthermore, Caspase-1 activity and IL-1-beta levels were elevated at 5 months, confirming that this pathway is indeed altered. Our results suggest that undegraded GAG activate the inflammasome pathway in MPS II and future studies could focus on blocking such pathway to better understand the role of this process to the pathogenesis of MPS II.

Indexed as

AnimalsBrainCaspase 1Cathepsin BDisease Models, AnimalInflammasomesInterleukin-1betaMiceMucopolysaccharidosis IINLR Family, Pyrin Domain-Containing 3 ProteinCaspase 1Cathepsin BInflammasomesInterleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteinCaspase-1CRISPR-Cas9Hunter syndromeInflammasomeInterleukin-1-betaMucopolysaccharidosis type IINRLP3

Identifiers

PMID32623553
OpenAlexW3038603981

What OpenQuestion 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 OpenQuestion graph.