Evidence map›Paper›PMID 31077035›Full record

ArticleNeuromolecular medicine2019

Exosomes Secreted by the Cocultures of Normal and Oxygen-Glucose-Deprived Stem Cells Improve Post-stroke Outcome.

Koteswara Rao Nalamolu, Ishwarya Venkatesh, Adithya Mohandass, Jeffrey D Klopfenstein, David M Pinson, David Z Wang, Adinarayana Kunamneni, Krishna Kumar Veeravalli

Open access · greenAbstract read
In one paragraph

Article in Neuromolecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 3 pooled it
2.2field-weighted citation impact, top 11% 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

27 citing papers in PubMed, 3 syntheses or guidelines pooled it, 44 citations in OpenAlex.

  1. Pooled it
  2. Pleiotropic Effects of Exosomes as a Therapy for Stroke Recovery.International journal of molecular sciences · 2020
    Pooled it
  3. Pooled it
  4. Review
  5. Review
  6. Review
  7. Extracellular Vesicles: The Invisible Heroes and Villains of COVID-19 Central Neuropathology.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
  8. Secretome as a Tool to Treat Neurological Conditions: Are We Ready?International journal of molecular sciences · 2023
    Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. Review of the Role of Mesenchymal Stem Cells and Exosomes Derived from Mesenchymal Stem Cells in the Treatment of Orthopedic Disease.Medical science monitor : international medical journal of experimental and clinical research · 2022
    Review
  20. Review
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

8 authors at 4 institutions in 1 country.

Koteswara Rao NalamoluDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine at Peoria, Peoria, IL, USA.
Ishwarya VenkateshDepartment of Internal Medicine, Rush University Medical Center, Chicago, IL, USA.
Adithya MohandassSchool of Pharmacy, College of Health Sciences, University of Wyoming, Laramie, WY, USA.
Jeffrey D KlopfensteinDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine at Peoria, Peoria, IL, USA.
David M PinsonDepartment of Pathology, University of Illinois College of Medicine at Peoria, Peoria, IL, USA.
David Z WangDepartment of Neurology, University of Illinois College of Medicine at Peoria, Peoria, IL, USA.
Adinarayana KunamneniDepartment of Medicine, Loyola University Medical Center, Chicago, IL, USA.
Krishna Kumar VeeravalliDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine at Peoria, Peoria, IL, USA. krishnav@uic.edu.ORCID http://orcid.org/0000-0002-2243-004X
University of Illinois Urbana-Champaign · USLoyola University Medical Center · USRush University Medical Center · USUniversity of Wyoming · US

Funding

MMP-12 and post-stroke brain damageR01NS102573 · NINDS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI VEERAVALLI, KRISHNA KUMAR · 2018 to 2022
$1.8M
NIH HHS 1R01NS102573-01A1NINDS NIH HHS R01 NS102573
6 · The paper itself

Abstract

Emerging stroke literature suggests that treatment of experimentally induced stroke with stem cells offered post-stroke neuroprotection via exosomes produced by these cells. Treatment with exosomes has great potential to overcome the limitations associated with cell-based therapies. However, in our preliminary studies, we noticed that the exosomes released from human umbilical cord blood-derived mesenchymal stem cells (MSCs) under standard culture conditions did not improve the post-stroke neurological outcome. Because of this apparent discrepancy, we hypothesized that exosome characteristics vary with the conditions of their production. Specifically, we suggest that the exosomes produced from the cocultures of regular and oxygen-glucose-deprived (OGD) MSCs in vitro would represent the exosomes produced from MSCs that are exposed to ischemic brain cells in vivo, and offer similar therapeutic benefits that the cell treatment would provide. We tested the efficacy of therapy with exosomes secreted from human umbilical cord blood (HUCB)-derived MSCs under in vitro hypoxic conditions on post-stroke brain damage and neurological outcome in a rat model of transient focal cerebral ischemia. We performed the TTC staining procedure as well as the neurological tests including the modified neurological severity scores (mNSS), the modified adhesive removal (sticky-tape), and the beam walking tests before ischemia and at regular intervals until 7 days reperfusion. Treatment with exosomes obtained from the cocultures of normal and OGD-induced MSCs reduced the infarct size and ipsilateral hemisphere swelling, preserved the neurological function, and facilitated the recovery of stroke-induced rats. Based on the results, we conclude that the treatment with exosomes secreted from MSCs at appropriate experimental conditions attenuates the post-stroke brain damage and improves the neurological outcome.

Indexed as

ExosomesAnimalsBody WeightBrain Damage, ChronicBrain IschemiaCell HypoxiaCoculture TechniquesFetal BloodGlucoseHumansHypoxia-Inducible Factor 1, alpha SubunitMaleMesenchymal Stem CellsOxygenPostural BalancePsychomotor PerformanceGlucoseHif1a protein, ratHypoxia-Inducible Factor 1, alpha SubunitOxygenBrain damageExosomesIschemiaNeurological recoveryReperfusionStem cells

Identifiers

PMID31077035
PMCPMC7272187
OpenAlexW2944151471

What OpenQuestion holds

Textmetadata
LicenceTDM
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.