Evidence map›Paper›PMID 31466320›Full record

ArticleCells2019

Differential Effects of Extracellular Vesicles of Lineage-Specific Human Pluripotent Stem Cells on the Cellular Behaviors of Isogenic Cortical Spheroids.

Mark Marzano, Julie Bejoy, Mujeeb R Cheerathodi, Li Sun, Sara B York, Jing Zhao, Takahisa Kanekiyo, Guojun Bu, David G Meckes, Yan Li

Open access · goldAbstract read
In one paragraph

Article in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

37 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article
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

10 authors at 3 institutions in 1 country.

Mark MarzanoDepartment of Chemical and Biomedical Engineering, FAMU-FSU College of Engineering, Florida State University, Tallahassee, FL 32310, USA.
Julie BejoyDepartment of Chemical and Biomedical Engineering, FAMU-FSU College of Engineering, Florida State University, Tallahassee, FL 32310, USA.
Mujeeb R CheerathodiDepartment of Biomedical Sciences, College of Medicine, Florida State University, Tallahassee, FL 32306, USA.
Li SunDepartment of Biomedical Sciences, College of Medicine, Florida State University, Tallahassee, FL 32306, USA.
Sara B YorkDepartment of Biomedical Sciences, College of Medicine, Florida State University, Tallahassee, FL 32306, USA.
Jing ZhaoDepartment of Neuroscience, Alzheimer's Disease Research Center, Mayo Clinic, Jacksonville, FL 32225, USA.
Takahisa KanekiyoDepartment of Neuroscience, Alzheimer's Disease Research Center, Mayo Clinic, Jacksonville, FL 32225, USA.
Guojun BuDepartment of Neuroscience, Alzheimer's Disease Research Center, Mayo Clinic, Jacksonville, FL 32225, USA.
David G MeckesDepartment of Biomedical Sciences, College of Medicine, Florida State University, Tallahassee, FL 32306, USA. David.Meckes@med.fsu.edu.ORCID 0000-0002-0836-2108
Yan LiDepartment of Chemical and Biomedical Engineering, FAMU-FSU College of Engineering, Florida State University, Tallahassee, FL 32310, USA. yli4@fsu.edu.
Florida State University · USFlorida A&M University - Florida State University College of Engineering · USMayo Clinic in Florida · US

Funding

Modulation of Host Cell Exosome Content and Function by EBV LMP1R01CA204621 · NCI · FLORIDA STATE UNIVERSITY · PI MECKES, DAVID G · 2016 to 2020
$2.2M
Engineering Extracellular Matrices in Forebrain Organoids for Studying Neural DegenerationR03NS102640 · NINDS · FLORIDA STATE UNIVERSITY · PI LI, YAN · 2017 to 2018
$143k
NCI NIH HHS R01 CA204621NINDS NIH HHS R03 NS102640
6 · The paper itself

Abstract

Extracellular vesicles (EVs) contribute to a variety of signaling processes and the overall physiological and pathological states of stem cells and tissues. Human induced pluripotent stem cells (hiPSCs) have unique characteristics that can mimic embryonic tissue development. There is growing interest in the use of EVs derived from hiPSCs as therapeutics, biomarkers, and drug delivery vehicles. However, little is known about the characteristics of EVs secreted by hiPSCs and paracrine signaling during tissue morphogenesis and lineage specification. Methods: In this study, the physical and biological properties of EVs isolated from hiPSC-derived neural progenitors (ectoderm), hiPSC-derived cardiac cells (mesoderm), and the undifferentiated hiPSCs (healthy iPSK3 and Alzheimer's-associated SY-UBH lines) were analyzed. Results: Nanoparticle tracking analysis and electron microscopy results indicate that hiPSC-derived EVs have an average size of 100-250 nm. Immunoblot analyses confirmed the enrichment of exosomal markers Alix, CD63, TSG101, and Hsc70 in the purified EV preparations. MicroRNAs including miR-133, miR-155, miR-221, and miR-34a were differently expressed in the EVs isolated from distinct hiPSC lineages. Treatment of cortical spheroids with hiPSC-EVs in vitro resulted in enhanced cell proliferation (indicated by BrdU+ cells) and axonal growth (indicated by β-tubulin III staining). Furthermore, hiPSC-derived EVs exhibited neural protective abilities in Aβ42 oligomer-treated cultures, enhancing cell viability and reducing oxidative stress. Our results demonstrate that the paracrine signaling provided by tissue context-dependent EVs derived from hiPSCs elicit distinct responses to impact the physiological state of cortical spheroids. Overall, this study advances our understanding of cell‒cell communication in the stem cell microenvironment and provides possible therapeutic options for treating neural degeneration.

Indexed as

BiomarkersCell DifferentiationCell ProliferationCells, CulturedCell SurvivalEctodermExtracellular VesiclesHumansInduced Pluripotent Stem CellsMesodermMicroRNAsNanoparticlesParacrine CommunicationParticle SizeSpheroids, CellularBiomarkersMicroRNAscardiac mesodermextracellular vesiclesinduced pluripotent stem cellsneural degenerationneural progenitors

Identifiers

PMID31466320
PMCPMC6770916
OpenAlexW2971022014

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.