Evidence map›Paper›PMID 39080300›Full record

ArticleScientific reports2024

Comprehensive proteomic analysis of the differential expression of 62 proteins following intracortical microelectrode implantation.

Sydney S Song, Lindsey N Druschel, Niveda M Kasthuri, Jaime J Wang, Jacob H Conard, E Ricky Chan, Abhinav P Acharya, Jeffrey R Capadona

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–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

7 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Sydney S Song *Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, 44106, USA.
Lindsey N Druschel *Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, 44106, USA.
Niveda M KasthuriDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, 44106, USA.
Jaime J WangDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, 44106, USA.
Jacob H ConardDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, 44106, USA.
E Ricky ChanCleveland Institute for Computational Biology, Case Western Reserve University, Cleveland, OH, 44106, USA.
Abhinav P AcharyaDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, 44106, USA.
Jeffrey R CapadonaDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, 44106, USA. jrc35@case.edu.

Funding

Integrated Neural Engineering and Rehabilitation Training ProgramT32EB004314 · NIBIB · CASE WESTERN RESERVE UNIVERSITY · PI Jeffrey R Capadona, Robert F. Kirsch · 2004 to 2026
$6.1M
Deploying Intracortical Electrode Arrays to Record and Stimulate in a Tissue VolumeR01NS131502 · NINDS · TEXAS A&M UNIVERSITY · PI Taylor H Ware · 2023 to 2026
$1.9M
National Institute for Biomedical Imaging and Bioengineering T32EB004314NIBIB NIH HHS T32 EB004314NINDS NIH HHS GRANT12635723NINDS NIH HHS NS131502NINDS NIH HHS R01 NS131502Rehabilitation Research and Development Service GRANT12418820Rehabilitation Research and Development Service GRANT12635707
6 · The paper itself

Abstract

Intracortical microelectrodes (IMEs) are devices designed to be implanted into the cerebral cortex for various neuroscience and neuro-engineering applications. A critical feature of IMEs is their ability to detect neural activity from individual neurons. Currently, IMEs are limited by chronic failure, largely considered to be caused by the prolonged neuroinflammatory response to the implanted devices. Over the past few years, the characterization of the neuroinflammatory response has grown in sophistication, with the most recent advances focusing on mRNA expression following IME implantation. While gene expression studies increase our broad understanding of the relationship between IMEs and cortical tissue, advanced proteomic techniques have not been reported. Proteomic evaluation is necessary to describe the diverse changes in protein expression specific to neuroinflammation, neurodegeneration, or tissue and cellular viability, which could lead to the further development of targeted intervention strategies designed to improve IME functionality. In this study, we have characterized the expression of 62 proteins within 180 μm of the IME implant site at 4-, 8-, and 16-weeks post-implantation. We identified potential targets for immunotherapies, as well as key pathways that contribute to neuronal dieback around the IME implant.

Indexed as

Cerebral CortexElectrodes, ImplantedMicroelectrodesProteomicsAnimalsMaleNeuronsProteomeRatsProteome

Identifiers

PMID39080300
PMCPMC11289480

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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.