Evidence map›Paper›PMID 35162938›Full record

ArticleInternational journal of molecular sciences2022

Culture Condition of Bone Marrow Stromal Cells Affects Quantity and Quality of the Extracellular Vesicles.

Amanda L Scheiber, Cierra A Clark, Takashi Kaito, Masahiro Iwamoto, Edwin M Horwitz, Yuka Imamura Kawasawa, Satoru Otsuru

Open access · goldAbstract readComparative Study
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 16 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 4 institutions in 2 countries.

Amanda L ScheiberDepartment of Orthopaedics, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Cierra A ClarkDepartment of Orthopaedics, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Takashi KaitoDepartment of Orthopaedic Surgery, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Masahiro IwamotoDepartment of Orthopaedics, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Edwin M HorwitzAflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta and Emory University Department of Pediatrics, Atlanta, GA 30322, USA.
Yuka Imamura KawasawaDepartments of Pharmacology and Biochemistry and Molecular Biology, Institute of Personalized Medicine, Penn State University, College of Medicine, Hershey, PA 17033, USA.
Satoru OtsuruDepartment of Orthopaedics, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
University of Maryland, Baltimore · USChildren's Healthcare of Atlanta · USOsaka University · JPPennsylvania State University · US

Funding

Mechanism of growth deficiency in dominant forms of osteogenesis imperfectaR01AR075733 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI OTSURU, SATORU · 2020 to 2024
$1.7M
Development of a novel therapy with Apolipoprotein E for osteogenesis imperfectaR21AR077654 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI OTSURU, SATORU · 2020 to 2021
$369k
Maryland Stem Cell Research Fund 2018-MSCRFD-4331NIAMS NIH HHS R01 AR075733NIAMS NIH HHS R01AR075733NIAMS NIH HHS R21 AR077654NIAMS NIH HHS R21AR077654
6 · The paper itself

Abstract

Extracellular vesicles (EVs) released by bone marrow stromal cells (BMSCs) have been shown to act as a transporter of bioactive molecules such as RNAs and proteins in the therapeutic actions of BMSCs in various diseases. Although EV therapy holds great promise to be a safer cell-free therapy overcoming issues related to cell therapy, manufacturing processes that offer scalable and reproducible EV production have not been established. Robust and scalable BMSC manufacturing methods have been shown to enhance EV production; however, the effects on EV quality remain less studied. Here, using human BMSCs isolated from nine healthy donors, we examined the effects of high-performance culture media that can rapidly expand BMSCs on EV production and quality in comparison with the conventional culture medium. We found significantly increased EV production from BMSCs cultured in the high-performance media without altering their multipotency and immunophenotypes. RNA sequencing revealed that RNA contents in EVs from high-performance media were significantly reduced with altered profiles of microRNA enriched in those related to cellular growth and proliferation in the pathway analysis. Given that pre-clinical studies at the laboratory scale often use the conventional medium, these findings could account for the discrepancy in outcomes between pre-clinical and clinical studies. Therefore, this study highlights the importance of selecting proper culture conditions for scalable and reproducible EV manufacturing.

Indexed as

Cell Culture TechniquesCell ProliferationCells, CulturedCulture MediaExtracellular VesiclesHealthy VolunteersHumansMesenchymal Stem CellsMicroRNAsSequence Analysis, RNASignal TransductionCulture MediaMicroRNAsbone marrow stromal cells (BMSCs)culture conditionextracellular vesicles (EVs)miRNAs

Identifiers

PMID35162938
PMCPMC8834965
OpenAlexW4206518207

What OpenQuestion holds

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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.