Evidence map›Paper›PMID 37508512›Full record

ArticleCells2023

Co-Aggregation and Parallel Aggregation of Specific Proteins in Major Mental Illness.

Bobana Samardžija, Maja Juković, Beti Zaharija, Éva Renner, Miklós Palkovits, Nicholas J Bradshaw

Open access · goldAbstract read
In one paragraph

Article in Cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

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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

6 authors at 2 institutions in 2 countries.

Bobana SamardžijaDepartment of Biotechnology, University of Rijeka, 51000 Rijeka, Croatia.ORCID 0000-0001-7745-2337
Maja JukovićDepartment of Biotechnology, University of Rijeka, 51000 Rijeka, Croatia.ORCID 0000-0002-2777-2698
Beti ZaharijaDepartment of Biotechnology, University of Rijeka, 51000 Rijeka, Croatia.ORCID 0000-0003-2183-7507
Éva RennerHuman Brain Tissue Bank & Laboratory, Semmelweis University, 1094 Budapest, Hungary.
Miklós PalkovitsHuman Brain Tissue Bank & Laboratory, Semmelweis University, 1094 Budapest, Hungary.ORCID 0000-0003-0578-0387
Nicholas J BradshawDepartment of Biotechnology, University of Rijeka, 51000 Rijeka, Croatia.ORCID 0000-0001-5581-8828
University of Rijeka · HRSemmelweis University · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDisrupted proteostasis is an emerging area of research into major depressive disorder. Several proteins have been implicated as forming aggregates specifically in the brains of subsets of patients with psychiatric illnesses. These proteins include CRMP1, DISC1, NPAS3 and TRIOBP-1. It is unclear, however, whether these proteins normally aggregate together in the same individuals and, if so, whether each protein aggregates independently of each other ("parallel aggregation") or if the proteins physically interact and aggregate together ("co-aggregation"). MATERIALS AND

methodsPost mortem insular cortex samples from major depressive disorder and Alzheimer's disease patients, suicide victims and control individuals had their insoluble fractions isolated and tested by Western blotting to determine which of these proteins are insoluble and, therefore, likely to be aggregating. The ability of the proteins to co-aggregate (directly interact and form common aggregate structures) was tested by systematic pairwise expression of the proteins in SH-SY5Y neuroblastoma cells, which were then examined by immunofluorescent microscopy.

resultsMany individuals displayed multiple insoluble proteins in the brain, although not enough to imply interaction between the proteins. Cell culture analysis revealed that only a few of the proteins analyzed can consistently co-aggregate with each other: DISC1 with each of CRMP1 and TRIOBP-1. DISC1 was able to induce aggregation of full length TRIOBP-1, but not individual domains of TRIOBP-1 when they were expressed individually.

conclusionsWhile specific proteins are capable of co-aggregating, and appear to do so in the brains of individuals with mental illness and potentially also with suicidal tendency, it is more common for such proteins to aggregate in a parallel manner, through independent mechanisms. This information aids in understanding the distribution of protein aggregates among mental illness patients and is therefore important for any future diagnostic or therapeutic approaches based on this aspect of mental illness pathology.

Indexed as

Major Depressive DisorderMental DisordersNeuroblastomaBasic Helix-Loop-Helix ProteinsBrainHumansProtein AggregatesBasic Helix-Loop-Helix ProteinsNPAS3 protein, humanProtein Aggregatesinsular cortexmental illnesspost mortem brain tissueprotein aggregationproteinopathysuicide

Identifiers

PMID37508512
PMCPMC10378145
OpenAlexW4384340960

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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.