Evidence map›Paper›PMID 39984653›Full record

ArticleNature cell biology2025

Blebbisomes are large, organelle-rich extracellular vesicles with cell-like properties.

Dennis K Jeppesen, Zachary C Sanchez, Noah M Kelley, James B Hayes, Jessica Ambroise, Emma N Koory, Evan Krystofiak, Nilay Taneja, Qin Zhang, Matthew M Dungan and 7 more

Abstract read
In one paragraph

Article in Nature cell biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing 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

52 citing papers in PubMed.

  1. Review
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  4. Article
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  7. Condensates on the Move: Midbody Remnants as Large, Translation-Competent Extracellular Vesicles.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
  8. Article
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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

17 authors.

Dennis K Jeppesen *Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA. dennis.k.jeppesen@vumc.org.ORCID 0000-0002-7480-8083
Zachary C Sanchez *Department of Cell and Developmental Biology, Vanderbilt University School of Medicine Basic Sciences, Nashville, TN, USA.ORCID 0000-0001-9075-1577
Noah M KelleyDepartment of Cell and Developmental Biology, Vanderbilt University School of Medicine Basic Sciences, Nashville, TN, USA.ORCID 0009-0002-7700-773X
James B HayesDepartment of Cell and Developmental Biology, Vanderbilt University School of Medicine Basic Sciences, Nashville, TN, USA.
Jessica AmbroiseDepartment of Cell and Developmental Biology, Vanderbilt University School of Medicine Basic Sciences, Nashville, TN, USA.
Emma N KooryDepartment of Cell and Developmental Biology, Vanderbilt University School of Medicine Basic Sciences, Nashville, TN, USA.
Evan KrystofiakDepartment of Cell and Developmental Biology, Vanderbilt University School of Medicine Basic Sciences, Nashville, TN, USA.ORCID 0000-0002-0043-6977
Nilay TanejaDepartment of Cell and Developmental Biology, Vanderbilt University School of Medicine Basic Sciences, Nashville, TN, USA.ORCID 0000-0002-9046-0953
Qin ZhangDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Matthew M DunganDepartment of Molecular Pathology and Immunology, Vanderbilt University Medical Center, Nashville, TN, USA.
Olivia L PerkinsDepartment of Cell and Developmental Biology, Vanderbilt University School of Medicine Basic Sciences, Nashville, TN, USA.
Matthew J TyskaDepartment of Cell and Developmental Biology, Vanderbilt University School of Medicine Basic Sciences, Nashville, TN, USA.ORCID 0000-0003-2238-6189
Ela W KnapikDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Kevin M DeanLydia Hill Department of Bioinformatics, University of Texas Southwestern, Dallas, TX, USA.ORCID 0000-0003-0839-2320
Amanda C DoranDepartment of Molecular Pathology and Immunology, Vanderbilt University Medical Center, Nashville, TN, USA.
Robert J CoffeyDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.ORCID 0000-0002-2180-3844
Dylan T BurnetteDepartment of Cell and Developmental Biology, Vanderbilt University School of Medicine Basic Sciences, Nashville, TN, USA. dylan.burnette@vanderbilt.edu.ORCID 0000-0002-2571-7038

Funding

Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MARY Kay WASHINGTON · 2002 to 2026
$29.9M
Vanderbilt-Ingram Cancer Center SPORE in Gastrointestinal CancerP50CA236733 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI STEPHEN W. FESIK · 2019 to 2026
$19.6M
Shaping the Microenvironment by DPEP1 Facilitates Adenoma ProgressionU54CA274367 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Martha J. Shrubsole · 2022 to 2026
$9.7M
Integrated approach to study early and late events in colonic neoplasia: mouse to manR35CA197570 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Robert J. Coffey · 2017 to 2026
$9.4M
UTSW-UNC Center for Cell Signaling AnalysisRM1GM145399 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI Kevin Michael Dean, Klaus M. Hahn · 2022 to 2026
$6.2M
Molecular basis of brush border assemblyR01DK095811 · NIDDK · VANDERBILT UNIVERSITY · PI MATTHEW J TYSKA · 2013 to 2026
$4.9M
Role of I-BAR proteins in enterocyte differentiationR01DK111949 · NIDDK · VANDERBILT UNIVERSITY · PI MATTHEW J TYSKA · 2017 to 2026
$4.2M
The assembly and function of cellular contractile systemsR35GM125028 · NIGMS · VANDERBILT UNIVERSITY · PI Dylan Tyler Burnette · 2017 to 2026
$4.2M
Critical Mediators of Inflammation Resolution and Immune Memory in AtherosclerosisR01HL159487 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DORAN, AMANDA C · 2021 to 2025
$3.2M
Acquisition of a Focused Ion Beam Scanning Electron Microscope with cryo-stageS10OD028704 · OD · VANDERBILT UNIVERSITY · PI TYSKA, MATTHEW J · 2022 to 2022
$1.6M
Advancing drug repositioning and development for Alzheimer's Disease using functional genomics and computational phenomicsR56AG068026 · NIA · VANDERBILT UNIVERSITY MEDICAL CENTER · PI GAMAZON, ERIC R · 2021 to 2022
$1.5M
Myosin-2 function in the enterocyte terminal webR01DK125546 · NIDDK · VANDERBILT UNIVERSITY · PI TYSKA, MATTHEW J · 2021 to 2024
$1.4M
American Heart Association (American Heart Association, Inc.) 1070985American Heart Association (American Heart Association, Inc.) 836090NCI NIH HHS P50 CA236733NCI NIH HHS R35 CA197570NCI NIH HHS U54 CA274367NHLBI NIH HHS R01 HL159487NIA NIH HHS R56 AG068026NIDDK NIH HHS P30 DK058404NIDDK NIH HHS R01 DK095811NIDDK NIH HHS R01 DK111949NIDDK NIH HHS R01 DK125546NIGMS NIH HHS R35 GM125028NIGMS NIH HHS RM1 GM145399NIH HHS S10 OD028704U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) R01HL159487U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R35GM125028U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) RM1GM145399U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) R56AG068026U.S. Department of Health & Human Services | NIH | NCI | Division of Cancer Epidemiology and Genetics, National Cancer Institute (National Cancer Institute Division of Cancer Epidemiology and Genetics) P50CA236733
6 · The paper itself

Abstract

Cells secrete a large variety of extracellular vesicles (EVs) to engage in cell-to-cell and cell-to-environment intercellular communication. EVs are functionally involved in many physiological and pathological processes by interacting with cells that facilitate transfer of proteins, lipids and genetic information. However, our knowledge of EVs is incomplete. Here we show that cells actively release exceptionally large (up to 20 µm) membrane-enclosed vesicles that exhibit active blebbing behavior, and we, therefore, have termed them blebbisomes. Blebbisomes contain an array of cellular organelles that include functional mitochondria and multivesicular endosomes, yet lack a definable nucleus. We show that blebbisomes can both secrete and internalize exosomes and microvesicles. Blebbisomes are released from normal and cancer cells, can be observed by direct imaging of cancer cells in vivo and are present in normal bone marrow. We demonstrate that cancer-derived blebbisomes contain a plethora of inhibitory immune checkpoint proteins, including PD-L1, PD-L2, B7-H3, VISTA, PVR and HLA-E. These data identify a very large, organelle-containing functional EV that act as cell-autonomous mobile communication centres capable of integrating and responding to signals in the extracellular environment.

Indexed as

Extracellular VesiclesNeoplasmsOrganellesAnimalsCell CommunicationCell Line, TumorEndosomesExosomesHumansMitochondria

Identifiers

PMID39984653
PMCPMC11906356

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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.