Evidence map›Paper›PMID 30361890›Full record

ArticleMolecular neurobiology2019

Increased Active OMI/HTRA2 Serine Protease Displays a Positive Correlation with Cholinergic Alterations in the Alzheimer's Disease Brain.

Taher Darreh-Shori, Sareh Rezaeianyazdi, Erica Lana, Sumonto Mitra, Anna Gellerbring, Azadeh Karami, Nenad Bogdanovic, Christina Unger Lithner, Bengt Winblad, Homira Behbahani

Open access · hybridAbstract read
In one paragraph

Article in Molecular neurobiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

16 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Article
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  5. Review
  6. Protease-independent control of parthanatos by HtrA2/Omi.Cellular and molecular life sciences : CMLS · 2023
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  8. Apoptotic proteins with non-apoptotic activity: expression and function in cancer.Apoptosis : an international journal on programmed cell death · 2023
    Review
  9. Neuron-specific transcriptomic signatures indicate neuroinflammation and altered neuronal activity in ASD temporal cortex.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  10. The in vitro treatment of mesenchymal stem cells for colorectal cancer cells.Medical oncology (Northwood, London, England) · 2023
    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

10 authors at 2 institutions in 1 country.

Taher Darreh-ShoriDivision of Clinical Geriatrics, Center for Alzheimer Research, NVS Department, Karolinska Institutet, Neo7th floor, 141 83, Huddinge, Sweden. taher.darreh-shori@ki.se.
Sareh RezaeianyazdiDivision of Neurogeriatrics, Center for Alzheimer Research, NVS Department, Karolinska Institutet, 141 83, Huddinge, Sweden.
Erica LanaDivision of Clinical Geriatrics, Center for Alzheimer Research, NVS Department, Karolinska Institutet, Neo7th floor, 141 83, Huddinge, Sweden.
Sumonto MitraDivision of Clinical Geriatrics, Center for Alzheimer Research, NVS Department, Karolinska Institutet, Neo7th floor, 141 83, Huddinge, Sweden.
Anna GellerbringDivision of Clinical Geriatrics, Center for Alzheimer Research, NVS Department, Karolinska Institutet, Neo7th floor, 141 83, Huddinge, Sweden.
Azadeh KaramiDivision of Clinical Geriatrics, Center for Alzheimer Research, NVS Department, Karolinska Institutet, Neo7th floor, 141 83, Huddinge, Sweden.
Nenad BogdanovicDivision of Neurogeriatrics, Center for Alzheimer Research, NVS Department, Karolinska Institutet, 141 83, Huddinge, Sweden.
Christina Unger LithnerDivision of Clinical Geriatrics, Center for Alzheimer Research, NVS Department, Karolinska Institutet, Neo7th floor, 141 83, Huddinge, Sweden.
Bengt WinbladDivision of Neurogeriatrics, Center for Alzheimer Research, NVS Department, Karolinska Institutet, 141 83, Huddinge, Sweden.
Homira BehbahaniDivision of Neurogeriatrics, Center for Alzheimer Research, NVS Department, Karolinska Institutet, 141 83, Huddinge, Sweden. homira.behbahani@ki.se.ORCID http://orcid.org/0000-0002-2612-0858
Karolinska Institutet · SEKarolinska University Hospital · SE

Funding

The international Alzheimer Association 2016-NIRG-391599The Swedish Research Council 2016-01806
6 · The paper itself

Abstract

OMI/HTRA2 (high-temperature requirement serine protease A2) is a mitochondrial serine protease involved in several cellular processes, including autophagy, chaperone activity, and apoptosis. Few studies on the role of OMI/HTRA2 in Alzheimer's disease (AD) are available, but none on its relationship with the cholinergic system and neurotrophic factors as well as other AD-related proteins. In this study, immunohistochemical analyses revealed that AD patients had a higher cytosolic distribution of OMI/HTRA2 protein compared to controls. Quantitative analyses on brain extracts indicated a significant increase in the active form of OMI/HTRA2 in the AD brain. Activated OMI/HTRA2 protein positively correlated with stress-associated read-through acetylcholinesterase activity. In addition, α7 nicotinic acetylcholine receptor gene expression, a receptor also known to be localized on the outer membrane of mitochondria, showed a strong correlation with OMI/HTRA2 gene expression in three different brain regions. Interestingly, the activated OMI/HTRA2 levels also correlated with the activity of the acetylcholine-biosynthesizing enzyme, choline acetyltransferase (ChAT); with levels of the neurotrophic factors, NGF and BDNF; with levels of the soluble fragments of amyloid precursor protein (APP); and with gene expression of the microtubule-associated protein tau in the examined brain regions. Overall, the results demonstrate increased levels of the mitochondrial serine protease OMI/HTRA2, and a coherent pattern of association between the activated form of OMI/HTRA2 and several key proteins involved in AD pathology. In this paper, we propose a new hypothetical model to highlight the importance and needs of further investigation on the role of OMI/HTRA2 in the mitochondrial function and AD.

Indexed as

AcetylcholineAcetylcholinesteraseAgedAged, 80 and overalpha7 Nicotinic Acetylcholine ReceptorAlzheimer DiseaseAmyloid beta-Protein PrecursorBiomarkersBrainBrain-Derived Neurotrophic FactorButyrylcholinesteraseFemaleGene Expression RegulationHigh-Temperature Requirement A Serine Peptidase 2HumansMaleAcetylcholineAcetylcholinesterasealpha7 Nicotinic Acetylcholine ReceptorAmyloid beta-Protein PrecursorBiomarkersBrain-Derived Neurotrophic FactorButyrylcholinesteraseHigh-Temperature Requirement A Serine Peptidase 2Nerve Growth Factortau ProteinsAlzheimer’s diseaseAPPCholinergic markersNGFOMI/HTRA2α7 nicotinic acetylcholine receptor

Identifiers

PMID30361890
PMCPMC6657433
OpenAlexW2898246389

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.