Evidence map›Paper›PMID 30830528›Full record

ArticleMolecular and cellular biochemistry2019

Proteomics analysis of Schwann cell-derived exosomes: a novel therapeutic strategy for central nervous system injury.

Zhijian Wei, Baoyou Fan, Han Ding, Yang Liu, Haoshuai Tang, Dayu Pan, Jiaxiao Shi, Pengyuan Zheng, Hongyu Shi, Heng Wu and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular and cellular biochemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

45 citing papers in PubMed, 81 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

12 authors at 2 institutions in 1 country.

Zhijian WeiDepartment of Orthopedics, Tianjin Medical University General Hospital, Tianjin, 300052, China.
Baoyou FanDepartment of Orthopedics, Tianjin Medical University General Hospital, Tianjin, 300052, China.
Han DingDepartment of Orthopedics, Tianjin Medical University General Hospital, Tianjin, 300052, China.
Yang LiuDepartment of Orthopedics, Tianjin Medical University General Hospital, Tianjin, 300052, China.
Haoshuai TangDepartment of Orthopedics, Tianjin Medical University General Hospital, Tianjin, 300052, China.
Dayu PanDepartment of Orthopedics, Tianjin Medical University General Hospital, Tianjin, 300052, China.
Jiaxiao ShiDepartment of Orthopedics, Tianjin Medical University General Hospital, Tianjin, 300052, China.
Pengyuan ZhengDepartment of Orthopedics, Tianjin Medical University General Hospital, Tianjin, 300052, China.
Hongyu ShiDepartment of Orthopedics, Tianjin Medical University General Hospital, Tianjin, 300052, China.
Heng WuTianjin Key Laboratory of Lung Cancer Metastasis and Tumor Microenvironment, Tianjin Lung Cancer Institute, Tianjin Medical University General Hospital, Tianjin, 300052, China.
Ang LiDepartment of Orthopedics, Henan Provincial People's Hospital, Zhengzhou, 450000, China.
Shiqing FengDepartment of Orthopedics, Tianjin Medical University General Hospital, Tianjin, 300052, China. sqfeng@tmu.edu.cn.
Tianjin Medical University General Hospital · CNHenan Provincial People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exosomes are nanometer-sized vesicles involved in intercellular communication, and they are released by various cell types. To learn about exosomes produced by Schwann cells (SCs) and to explore their potential function in repairing the central nervous system (CNS), we isolated exosomes from supernatants of SCs by ultracentrifugation, characterized them by electron microscopy and immunoblotting and determined their protein profile using proteomic analysis. The results demonstrated that Schwann cell-derived exosomes (SCDEs) were, on average, 106.5 nm in diameter, round, and had cup-like concavity and expressed exosome markers CD9 and Alix but not tumor susceptibility gene (TSG) 101. We identified a total of 433 proteins, among which 398 proteins overlapped with the ExoCarta database. According to their specific functions, we identified 12 proteins that are closely related to CNS repair and classified them by different potential mechanisms, such as axon regeneration and inflammation inhibition. Gene Oncology analysis indicated that SCDEs are mainly involved in signal transduction and cell communication. Biological pathway analysis showed that pathways are mostly involved in exosome biogenesis, formation, uptake and axon regeneration. Among the pathways, the neurotrophin, PI3K-Akt and cAMP signaling pathways played important roles in CNS repair. Our study isolated SCDEs, unveiled their contents, presented potential neurorestorative proteins and pathways and provided a rich proteomics data resource that will be valuable for future studies of the functions of individual proteins in neurodegenerative diseases.

Indexed as

ProteomicsAnimalsBiomarkersExosomesMaleNerve Tissue ProteinsRatsRats, WistarSchwann CellsSciatic NerveBiomarkersNerve Tissue ProteinsCentral nervous systemExosomesProteomicsSchwann cell

Identifiers

PMID30830528
PMCPMC6548868
OpenAlexW2920106313

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.