Evidence map›Paper›PMID 38786083›Full record

ArticleCells2024

hTERT-Immortalized Mesenchymal Stem Cell-Derived Extracellular Vesicles: Large-Scale Manufacturing, Cargo Profiling, and Functional Effects in Retinal Epithelial Cells.

Jessica Hindle, Anastasia Williams, Yuriy Kim, Dongsung Kim, Kajal Patil, Pooja Khatkar, Quinn Osgood, Collin Nelson, David A Routenberg, Marissa Howard and 3 more

Abstract read
In one paragraph

Article in Cells, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

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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

13 authors.

Jessica HindleATCC, Manassas, VA 20110, USA.
Anastasia WilliamsLaboratory of Molecular Virology, School of Systems Biology, George Mason University, Manassas, VA 20110, USA.ORCID 0009-0002-9049-2530
Yuriy KimLaboratory of Molecular Virology, School of Systems Biology, George Mason University, Manassas, VA 20110, USA.ORCID 0000-0001-8658-6863
Dongsung KimATCC, Manassas, VA 20110, USA.
Kajal PatilLaboratory of Molecular Virology, School of Systems Biology, George Mason University, Manassas, VA 20110, USA.
Pooja KhatkarLaboratory of Molecular Virology, School of Systems Biology, George Mason University, Manassas, VA 20110, USA.ORCID 0000-0003-3842-5146
Quinn OsgoodATCC, Manassas, VA 20110, USA.
Collin NelsonMeso Scale Diagnostics, L.L.C., Rockville, MD 20850, USA.
David A RoutenbergMeso Scale Diagnostics, L.L.C., Rockville, MD 20850, USA.ORCID 0009-0001-6200-5646
Marissa HowardCenter for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA 20110, USA.
Lance A LiottaCenter for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA 20110, USA.
Fatah KashanchiLaboratory of Molecular Virology, School of Systems Biology, George Mason University, Manassas, VA 20110, USA.ORCID 0000-0001-9681-2780
Heather BranscomeATCC, Manassas, VA 20110, USA.

Funding

HIV1 INHIBITION USING TAT PEPTIDE DERIVATIVESR01AI043894 · NIAID · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI KASHANCHI, FATAH · 1999 to 2015
$4.4M
Cell-derived extracellular vesicle mediated epigenetic silencing of HIV in the brainR01MH134389 · NIMH · GEORGE MASON UNIVERSITY · PI Fatah Kashanchi · 2023 to 2026
$2.0M
HIV neuropathogenesis related to exosomes containing HIV non-coding RNAsR01NS099029 · NINDS · GEORGE MASON UNIVERSITY · PI KASHANCHI, FATAH · 2016 to 2020
$1.9M
Effect on CBD on Exosome release from CNS infected cellsR21DA050176 · NIDA · GEORGE MASON UNIVERSITY · PI KASHANCHI, FATAH · 2020 to 2021
$447k
Effect of chromatin remodelers/modifiers on HIV-1 Tat activated transcriptionR21AI074410 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI KASHANCHI, FATAH · 2009 to 2010
$432k
A radiation-induced cellular stress activates HIV and induces killing of infected cellsR21AI127351 · NIAID · GEORGE MASON UNIVERSITY · PI KASHANCHI, FATAH · 2016 to 2017
$418k
HIV-1 TAR derived miRNA: Implications for Latency and PathogenesisR21AI078859 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI KASHANCHI, FATAH · 2009 to 2010
$400k
NIAID NIH HHS R01 AI043894NIAID NIH HHS R21 AI074410NIAID NIH HHS R21 AI078859NIAID NIH HHS R21 AI127351NIDA NIH HHS R21 DA050176NIH HHS AI078859, AI074410, AI127351-01, AI043894, NS099029, DA050176, and R01MH13438901NIMH NIH HHS R01 MH134389NINDS NIH HHS R01 NS099029
6 · The paper itself

Abstract

As the economic burden associated with vision loss and ocular damage continues to rise, there is a need to explore novel treatment strategies. Extracellular vesicles (EVs) are enriched with various biological cargo, and there is abundant literature supporting the reparative and immunomodulatory properties of stem cell EVs across a broad range of pathologies. However, one area that requires further attention is the reparative effects of stem cell EVs in the context of ocular damage. Additionally, most of the literature focuses on EVs isolated from primary stem cells; the use of EVs isolated from human telomerase reverse transcriptase (hTERT)-immortalized stem cells has not been thoroughly examined. Using our large-scale EV-manufacturing platform, we reproducibly manufactured EVs from hTERT-immortalized mesenchymal stem cells (MSCs) and employed various methods to characterize and profile their associated cargo. We also utilized well-established cell-based assays to compare the effects of these EVs on both healthy and damaged retinal pigment epithelial cells. To the best of our knowledge, this is the first study to establish proof of concept for reproducible, large-scale manufacturing of hTERT-immortalized MSC EVs and to investigate their potential reparative properties against damaged retinal cells. The results from our studies confirm that hTERT-immortalized MSC EVs exert reparative effects in vitro that are similar to those observed in primary MSC EVs. Therefore, hTERT-immortalized MSCs may represent a more consistent and reproducible platform than primary MSCs for generating EVs with therapeutic potential.

Indexed as

Epithelial CellsExtracellular VesiclesMesenchymal Stem CellsRetinal Pigment EpitheliumTelomeraseHumansTelomeraseTERT protein, humanextracellular vesicles (EVs)hTERT-immortalized mesenchymal stem cellsionizing radiation (IR)retinal pigment epithelium (RPE) cells

Identifiers

PMID38786083
PMCPMC11120263

What OpenQuestion holds

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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.