Evidence map›Paper›PMID 35053007›Full record

ArticleBiology2021

Proteomic Analysis of Exosomes Secreted from Human Alpha-1 Antitrypsin Overexpressing Mesenchymal Stromal Cells.

Hua Wei, Erica Green, Lauren Ball, Hongkuan Fan, Jennifer Lee, Charlie Strange, Hongjun Wang

Open access · goldAbstract read
In one paragraph

Article in Biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

9 citing papers in PubMed, 11 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

7 authors at 2 institutions in 1 country.

Hua WeiDepartments of Surgery, Medical University of South Carolina, CRI 410, 173 Ashley Avenue, Charleston, SC 29425, USA.ORCID 0000-0002-0369-5130
Erica GreenDepartments of Surgery, Medical University of South Carolina, CRI 410, 173 Ashley Avenue, Charleston, SC 29425, USA.ORCID 0000-0003-2832-5301
Lauren BallCell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina, CRI 311, 173 Ashley Avenue, Charleston, SC 29425, USA.
Hongkuan FanPathology and Laboratory Medicine, Medical University of South Carolina, CRI 610, 173 Ashley Avenue, Charleston, SC 29425, USA.
Jennifer LeeWellesley College, Wellesley, MA 02481, USA.
Charlie StrangeDepartment of Medicine, Medical University of South Carolina, CSB 816, 96 Jonathan Lucas St., Charleston, SC 29425, USA.ORCID 0000-0002-8109-8067
Hongjun WangDepartments of Surgery, Medical University of South Carolina, CRI 410, 173 Ashley Avenue, Charleston, SC 29425, USA.ORCID 0000-0001-7421-1917
Medical University of South Carolina · USWellesley College · US

Funding

Proteomics CoreP30DK123704 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI DON C. ROCKEY · 2020 to 2026
$8.8M
Cellular Therapy for Type 1 Diabetes using Mesenchymal Stem CellsR01DK118529 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI WANG, HONGJUN · 2019 to 2025
$3.8M
Autologous BM-MSCs and Islet Co-transplantation to Enhance Islet Survival and Function in TP-IAT PatientsR01DK126454 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI WANG, HONGJUN · 2021 to 2025
$3.2M
Novel Gene and Stem Cell Therapy for Type 1 DiabetesR01DK120394 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI WANG, HONGJUN · 2018 to 2021
$2.2M
Alpha1 Anti-trypsin Enhances Islet Autograft SurvivalR01DK105183 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI WANG, HONGJUN · 2016 to 2020
$2.0M
Orbitrap Fusion Lumos ETD Mass SpectrometerS10OD025126 · OD · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BALL, LAUREN ELIZABETH · 2018 to 2018
$991k
hAAT-engineered Mesenchymal Stem Cells for the Treatment of Chronic PainI01BX004536 · VA · RALPH H JOHNSON VA MEDICAL CENTER · PI Hongjun Wang · 2020 to 2026
–
BLRD VA I01 BX004536department of Veteran Affairs VA-ORD BLR&D Merit I01BX004536NIDDK NIH HHS 1R01DK105183, 1R01 DK118529, 1R01DK1264 and 1R01DK120394 andNIDDK NIH HHS P30 DK123704NIDDK NIH HHS R01 DK105183NIDDK NIH HHS R01 DK118529NIDDK NIH HHS R01 DK120394NIDDK NIH HHS R01 DK126454NIH HHS S10 OD025126
6 · The paper itself

Abstract

Extracellular vesicles (EVs) mediate many therapeutic effects of stem cells during cellular therapies. Bone marrow-derived mesenchymal stromal cells (BM-MSCs) were manufactured to overexpress the human antiprotease alpha-1 antitrypsin (hAAT) and studied to compare the EV production compared to lentivirus treated control MSCs. The goal of this study was to compare protein profiles in the EVs/exosomes of control and hAAT-MSCs using unbiased, high resolution liquid chromatography and mass spectrometry to explore differences. Nanoparticle tracking analysis (NTA) showed that the particle size of the EVs from control MSCs or hAAT-MSCs ranged from 30 to 200 nm. Both MSCs and hAAT-MSCs expressed exosome-associated proteins, including CD63, CD81, and CD9. hAAT-MSCs also expressed high levels of hAAT. We next performed proteomic analysis of EVs from three healthy donor cell lines. Exosomes collected from cell supernatant were classified by GO analysis which showed proteins important to cell adhesion and extracellular matrix organization. However, there were differences between exosomes from control MSCs and hAAT-MSCs in cytokine signaling of the immune system, stem cell differentiation, and carbohydrate metabolism (

Indexed as

alpah-1 antitrypsinexosomeextracellular vesiclesmesenchymal stromal cellstherapy

Identifiers

PMID35053007
PMCPMC8773149
OpenAlexW4200239541

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.