Evidence map›Paper›PMID 42144122›Full record

ArticleMitochondrion2026

Electron microscopy visualization of cell-free mitochondrial DNA-associated vesicular structures in human plasma, serum, and saliva.

Alexandra Volos, Soah Grace Franklin, Jeremy Michelson, Shannon Rausser, Jonathan R Brestoff, Martin Picard

Abstract read
In one paragraph

Article in Mitochondrion, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Alexandra VolosDepartment of Psychiatry, Division of Behavioral Medicine, Columbia University Irving Medical Center, New York, NY 10032, United States.
Soah Grace FranklinDepartment of Psychiatry, Division of Behavioral Medicine, Columbia University Irving Medical Center, New York, NY 10032, United States.
Jeremy MichelsonDepartment of Psychiatry, Division of Behavioral Medicine, Columbia University Irving Medical Center, New York, NY 10032, United States.
Shannon RausserDepartment of Psychiatry, Division of Behavioral Medicine, Columbia University Irving Medical Center, New York, NY 10032, United States.
Jonathan R BrestoffDepartment of Pathology and Immunology, Washington University School of Medicine, St Louis, MO 63110, USA.
Martin PicardDepartment of Psychiatry, Division of Behavioral Medicine, Columbia University Irving Medical Center, New York, NY 10032, United States; Department of Neurology, H. Houston Merritt Center for Neurological and Mitochondrial Disorders, Columbia University Irving Medical Center, New York, New York 10032, United States; New York State Psychiatric Institute, New York, NY 10032, United States; Robert N Butler Columbia Aging Center, Mailman School of Public Health, New York, NY 10032, United States. Electronic address: martin.picard@columbia.edu.

Funding

Transduction of Psychological Stress into Systematic Inflammation by Mitochondrial DNA SignalingR01MH119336 · NIMH · NEW YORK STATE PSYCHIATRIC INSTITUTE DBA RESEARCH FOUNDATION FOR MENTAL HYGIENE, INC · PI KAUFMAN, BRETT A, MARSLAND, ANNA L · 2019 to 2023
$3.4M
NIMH NIH HHS R01 MH119336
6 · The paper itself

Abstract

Human biofluids contain cell-free mitochondrial DNA (cf-mtDNA) and extracellular mitochondria (ex-Mito), creating the challenge of defining their origins, destinations, mechanisms of regulation, and biological purpose(s). To expand our understanding of vesicular structures across human biofluids, we present a descriptive electron microscopy analysis of circulating particles from cf-mtDNA-enriched plasma (citrate, heparin, and EDTA), serum (red and gold top), and saliva collected from ten healthy participants (5 females, 5 males, mean age 44.9 years). Ex-mito and extracellular vesicles (EVs) were isolated by centrifugation followed by size-exclusion chromatography, imaged by transmission electron microscopy, and morphometrically analyzed. In parallel, cf-mtDNA was quantified in each biofluid to confirm enrichment. The resulting catalog of the most common circulating particles in plasma, serum, and saliva show that circulating double-membrane extracellular particles are present across human biofluids, along with EVs and other particle types. Combining imaging with cf-mtDNA quantification, we show that individuals with higher plasma cf-mtDNA concentrations tend to contain more double-membrane, ex-Mito-like particles. These preliminary and largely qualitative results do not directly demonstrate but are consistent with the concept of mitochondria transfer and/or signaling between cells and tissues. The image inventory provided here expands our knowledge of cell-free mitochondrial biology and provides a resource to inform biofluid selection and technical considerations in future studies quantifying ex-Mito and cf-mtDNA.

Indexed as

Cell-Free Nucleic AcidsDNA, MitochondrialExtracellular VesiclesPlasmaSalivaSerumAdultFemaleHumansMaleMicroscopy, Electron, TransmissionMiddle AgedMitochondriaCell-Free Nucleic AcidsDNA, Mitochondrialcell-free materialcirculatinghumanimage repositoryimagingmicroscopymitochondriastudy designvesicles

Identifiers

PMID42144122
PMCPMC13403135

What OpenQuestion holds

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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.