Evidence map›Paper›PMID 39084466›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2024

Mitochondria-containing extracellular vesicles from mouse vs. human brain endothelial cells for ischemic stroke therapy.

Kandarp M Dave, Venugopal R Venna, Krithika S Rao, Donna B Stolz, Bodhi Brady, Victoria A Quaicoe, Michael E Maniskas, Ella E Hildebrand, Dawson Green, Mingxi Chen and 5 more

Abstract readComparative Study
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

  1. Sequential-RSC pharmaceutics · 2026
    Article
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  9. Therapeutic and diagnostic potential of extracellular vesicle (EV)-mediated intercellular transfer of mitochondria and mitochondrial components.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2026
    Review
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  14. Article
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  20. Endothelial mitochondria in the blood-brain barrier.Fluids and barriers of the CNS · 2025
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Kandarp M DaveGraduate School of Pharmaceutical Sciences, Duquesne University, Pittsburgh, PA, United States of America.
Venugopal R VennaDepartment of Neurology, McGovern Medical School, University of Texas Health Science Center, Houston, TX, United States of America.
Krithika S RaoPittsburgh Heart Lung Blood Vascular Institute, University of Pittsburgh Medical School, Pittsburgh, PA, United States of America.
Donna B StolzCenter for Biologic Imaging, University of Pittsburgh Medical School, Pittsburgh, PA, United States of America.
Bodhi BradyHuman Biology, South Dakota State University, Brookings, SD, United States of America.
Victoria A QuaicoeDepartment of Neurology, McGovern Medical School, University of Texas Health Science Center, Houston, TX, United States of America.
Michael E ManiskasDepartment of Neurology, McGovern Medical School, University of Texas Health Science Center, Houston, TX, United States of America.
Ella E HildebrandGraduate School of Pharmaceutical Sciences, Duquesne University, Pittsburgh, PA, United States of America; Department of Psychology, Westminster College, New Wilmington, PA, United States of America.
Dawson GreenGraduate School of Pharmaceutical Sciences, Duquesne University, Pittsburgh, PA, United States of America.
Mingxi ChenDepartment of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, PA, United States of America.
Jadranka MilosevicDepartment of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, PA, United States of America; Captis Diagnostics Inc, Pittsburgh, PA, United States of America.
Si-Yang ZhengDepartment of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, PA, United States of America.
Sruti S ShivaPittsburgh Heart Lung Blood Vascular Institute, University of Pittsburgh Medical School, Pittsburgh, PA, United States of America; Department of Pharmacology and Chemical Biology, University of Pittsburgh Medical School, Pittsburgh, PA, United States of America.
Louise D McCulloughDepartment of Neurology, McGovern Medical School, University of Texas Health Science Center, Houston, TX, United States of America.
Devika S ManickamGraduate School of Pharmaceutical Sciences, Duquesne University, Pittsburgh, PA, United States of America. Electronic address: soundaramanickd@duq.edu.

Funding

Pain and Neurodegenerative Undergraduate Research Experiences: Interacting with community partners to build specialized and enhanced neurologic disease programs for undergraduates.R25NS100118 · NINDS · DUQUESNE UNIVERSITY · PI MICHAEL CASCIO, David Bruce Heisler · 2018 to 2026
$825k
NINDS NIH HHS R25 NS100118
6 · The paper itself

Abstract

Ischemic stroke-induced mitochondrial dysfunction in the blood-brain barrier-forming brain endothelial cells (BECs) results in long-term neurological dysfunction post-stroke. We previously reported data from a pilot study where intravenous administration of human BEC (hBEC)-derived mitochondria-containing extracellular vesicles (EVs) showed a potential efficacy signal in a mouse middle cerebral artery occlusion (MCAo) model of stroke. We hypothesized that EVs harvested from donor species homologous to the recipient species (e.g., mouse) may improve therapeutic efficacy, and therefore, use of mouse BEC (mBEC)-derived EVs may improve post-stroke outcomes in MCAo mice. We investigated potential differences in the mitochondria transfer of EVs derived from the same species as the recipient cell (mBEC-EVs and recipient mBECs or hBECs-EVs and recipient hBECs) vs. cross-species EVs and recipient cells (mBEC-EVs and recipient hBECs or vice versa). Our results showed that while both hBEC- and mBEC-EVs transferred EV mitochondria, mBEC-EVs outperformed hBEC-EVs in increasing ATP levels and improved recipient mBEC mitochondrial function via increasing oxygen consumption rates. mBEC-EVs significantly reduced brain infarct volume and neurological deficit scores compared to vehicle-injected MCAo mice. The superior therapeutic efficacy of mBEC-EVs in MCAo mice support the continued use of mBEC-EVs to optimize the therapeutic potential of mitochondria-containing EVs in preclinical mouse models.

Indexed as

BrainEndothelial CellsExtracellular VesiclesInfarction, Middle Cerebral ArteryIschemic StrokeMice, Inbred C57BLMitochondriaAnimalsBlood-Brain BarrierCells, CulturedHumansMaleMiceBBB metabolic protectionBrain endothelial cells (BECs)Exosomes (120K EVs)Extracellular vesicles (EVs)Ischemic strokeMicrovesicles (20K EVs)Mitochondria

Identifiers

PMID39084466
PMCPMC13333119

What OpenQuestion holds

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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.