Evidence map›Paper›PMID 33579698›Full record

ArticleScience advances2021

Mitovesicles are a novel population of extracellular vesicles of mitochondrial origin altered in Down syndrome.

Pasquale D'Acunzo, Rocío Pérez-González, Yohan Kim, Tal Hargash, Chelsea Miller, Melissa J Alldred, Hediye Erdjument-Bromage, Sai C Penikalapati, Monika Pawlik, Mitsuo Saito and 5 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 184 papers.

0numbers the graph read from it
0cells of the map it votes in
184citing papers in PubMed
16.6field-weighted citation impact, top 1% 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

184 citing papers in PubMed, 263 citations in OpenAlex.

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  14. Alpha-synuclein fibrils induce budding of mitochondrial-derived vesicles.Proceedings of the National Academy of Sciences of the United States of America · 2026
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124 more citing papers are in PubMed but not listed here.

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

15 authors at 2 institutions in 1 country.

Pasquale D'AcunzoCenter for Dementia Research, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, NY 10962, USA.ORCID 0000-0001-7237-0076
Rocío Pérez-GonzálezCenter for Dementia Research, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, NY 10962, USA.ORCID 0000-0002-0641-2001
Yohan KimCenter for Dementia Research, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, NY 10962, USA.ORCID 0000-0003-2550-8751
Tal HargashCenter for Dementia Research, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, NY 10962, USA.ORCID 0000-0001-7173-6195
Chelsea MillerCenter for Dementia Research, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, NY 10962, USA.
Melissa J AlldredCenter for Dementia Research, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, NY 10962, USA.ORCID 0000-0002-5701-0694
Hediye Erdjument-BromageDepartment of Cell Biology, New York University School of Medicine, New York, NY 10016, USA.ORCID 0000-0003-0224-3594
Sai C PenikalapatiCenter for Dementia Research, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, NY 10962, USA.ORCID 0000-0002-3389-9302
Monika PawlikCenter for Dementia Research, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, NY 10962, USA.ORCID 0000-0003-0138-7529
Mitsuo SaitoDepartment of Psychiatry, New York University School of Medicine, New York, NY 10016, USA.
Mariko SaitoDepartment of Psychiatry, New York University School of Medicine, New York, NY 10016, USA.ORCID 0000-0001-9383-4458
Stephen D GinsbergCenter for Dementia Research, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, NY 10962, USA.ORCID 0000-0002-1797-4288
Thomas A NeubertDepartment of Cell Biology, New York University School of Medicine, New York, NY 10016, USA.ORCID 0000-0001-7049-2088
Chris N GoulbourneCenter for Dementia Research, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, NY 10962, USA.
Efrat LevyCenter for Dementia Research, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, NY 10962, USA. efrat.levy@nki.rfmh.org.ORCID 0000-0001-6890-6763
Nathan Kline Institute for Psychiatric Research · USNew York University · US

Funding

Uncovering Alzheimer's disease risk mechanisms through neuron-specific analysis of autophagy and endosomal-lysosomal functionP01AG017617 · NIA · NATHAN S. KLINE INSTITUTE FOR PSYCH RES · PI NIXON, RALPH A. · 2000 to 2021
$40.0M
Neuropathology and inflammation in a nonhuman primate model of insulin resistance/metabolic syndromeR01AG085572 · NIA · UNIVERSITY OF CALIFORNIA AT DAVIS · PI STEPHEN D GINSBERG, PETER J HAVEL · 2024 to 2026
$3.8M
Neuronal Protective Apolipoprotein E2-mediated endocytic and exocytic pathwaysRF1AG057517 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI LEVY, EFRAT, MATHEWS, PAUL M · 2017 to 2020
$2.4M
Brain exosomes mediate cocaine-induced addictionR01DA044489 · NIDA · NATHAN S. KLINE INSTITUTE FOR PSYCH RES · PI LEVY, EFRAT, SAITO, MARIKO · 2017 to 2021
$2.2M
Preventing early events in Aβ-driven pathology in vivoR01AG056732 · NIA · NATHAN S. KLINE INSTITUTE FOR PSYCH RES · PI LEVY, EFRAT · 2017 to 2021
$2.0M
LTQ-Orbitrap Mass Spectrometer.S10RR027990 · NCRR · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI NEUBERT, THOMAS A · 2011 to 2011
$600k
NCRR NIH HHS S10 RR027990NIA NIH HHS P01 AG017617NIA NIH HHS R01 AG056732NIA NIH HHS R01 AG085572NIA NIH HHS RF1 AG057517NIDA NIH HHS R01 DA044489
6 · The paper itself

Abstract

Mitochondrial dysfunction is an established hallmark of aging and neurodegenerative disorders such as Down syndrome (DS) and Alzheimer's disease (AD). Using a high-resolution density gradient separation of extracellular vesicles (EVs) isolated from murine and human DS and diploid control brains, we identify and characterize a previously unknown population of double-membraned EVs containing multiple mitochondrial proteins distinct from previously described EV subtypes, including microvesicles and exosomes. We term these newly identified mitochondria-derived EVs "mitovesicles." We demonstrate that brain-derived mitovesicles contain a specific subset of mitochondrial constituents and that their levels and cargo are altered during pathophysiological processes where mitochondrial dysfunction occurs, including in DS. The development of a method for the selective isolation of mitovesicles paves the way for the characterization in vivo of biological processes connecting EV biology and mitochondria dynamics and for innovative therapeutic and diagnostic strategies.

Indexed as

Alzheimer DiseaseDown SyndromeExosomesExtracellular VesiclesAnimalsHumansMice

Identifiers

PMID33579698
PMCPMC7880603
OpenAlexW3126430521

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

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.