Evidence map›Paper›PMID 39218796›Full record

ArticleCNS neuroscience & therapeutics2024

Sortilin is associated with progranulin deficiency and autism-like behaviors in valproic acid-induced autism rats.

Ailing Liao, Wenxia Zheng, Shali Wang, Nashi Wang, Yingbo Li, Di Chen, Yan Wang

Abstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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, 1 synthesis or guideline pooled it.

  1. Pooled it
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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

7 authors.

Ailing LiaoNHC Key Laboratory of Birth Defects and Reproductive Health, Chongqing Population and Family Planning Science and Technology Research Institute, Chongqing, China.ORCID 0009-0006-8573-6958
Wenxia ZhengInstitute of Neuroscience, School of Basic Medical Science, Chongqing Medical University, Chongqing, China.
Shali Wang
Nashi WangLibrary/Archive, Chongqing Medical University, Chongqing, China.
Yingbo Li
Di ChenInstitute of Neuroscience, School of Basic Medical Science, Chongqing Medical University, Chongqing, China.
Yan WangInstitute of Neuroscience, School of Basic Medical Science, Chongqing Medical University, Chongqing, China.

Funding

Natural Science Foundation of Chongqing, China cstc2021jcyj-msxmX0065Science and technology research program of Chongqing Education Commission of China. KJQN202300437the Chongqing Children's Aid Foundation (Life and Social Interaction Enhancement Program for Children with Autism
6 · The paper itself

Abstract

introductionNeuroinflammation and microglial activation-related dendritic injury contribute to the pathogenesis of Autism Spectrum Disorder (ASD). Previous studies show that Progranulin (PGRN) is a growth factor associated with inflammation and synaptic development, but the role of PGRN in autism and the mechanisms underlying changes in PGRN expression remain unclear.

aimsTo investigate the impact of PGRN in autism, we stereotactically injected recombinant PGRN into the hippocampus of ASD model rats. Additionally, we explored the possibility that sortilin may be the factor behind the alterations in PGRN by utilizing SORT1 knockdown. Ultimately, we aimed to identify potential targets for the treatment of autism.

resultsPGRN could alleviate inflammatory responses, protect neuronal dendritic spines, and ameliorate autism-like behaviors. Meanwhile, elevated expression of sortilin and decreased levels of PGRN were observed in both ASD patients and rats. Enhanced sortilin levels facilitated PGRN internalization into lysosomes. Notably, suppressing SORT1 expression amplified PGRN levels, lessened microglial activation, and mitigated inflammation, thereby alleviating autism-like behaviors.

conclusionCollectively, our findings highlight elevated sortilin levels in ASD rat brains, exacerbating dendrite impairment by affecting PGRN expression. PGRN supplementation and SORT1 knockdown hold potential as therapeutic strategies for ASD.

Indexed as

Adaptor Proteins, Vesicular TransportAutistic DisorderProgranulinsValproic AcidAnimalsDendritic SpinesFemaleHippocampusHumansMaleMicrogliaRatsRats, Sprague-DawleySortilinAdaptor Proteins, Vesicular TransportGRN protein, humanGrn protein, ratProgranulinsSortilinValproic Acidautism spectrum disorderdendritesinflammationNF‐κB pathwayPGRNSORT1

Identifiers

PMID39218796
PMCPMC11366450

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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.