Evidence mapPaperPMID 41353187Full record

ArticleFluids and barriers of the CNS2025

Neutrophil-secreted extracellular vesicles induce blood-brain barrier leakage and tight junction disruption.

Luis Arteaga-Blanco, Maliheh Najari Beidokhti, Nuria Villalba, Lindsay Swaby, Byeong J Cha, Cemre Kayisli, Yao Yao, Mack H Wu, Sarah Y Yuan

Abstract read
In one paragraph

Article in Fluids and barriers of the CNS, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

9 authors.

Luis Arteaga-BlancoDepartment of Surgery, University of South Florida Morsani College of Medicine, 12901 Bruce B. Downs Blvd, MDC 16, Tampa, FL, 33612, USA.
Maliheh Najari BeidokhtiDepartment of Molecular Pharmacology and Physiology, University of South Florida Morsani College of Medicine, Bruce B. Downs Blvd, MDC 8, Tampa, FL, 33612, USA.
Nuria VillalbaDepartment of Molecular Pharmacology and Physiology, University of South Florida Morsani College of Medicine, Bruce B. Downs Blvd, MDC 8, Tampa, FL, 33612, USA.
Lindsay SwabyDepartment of Molecular Pharmacology and Physiology, University of South Florida Morsani College of Medicine, Bruce B. Downs Blvd, MDC 8, Tampa, FL, 33612, USA.
Byeong J ChaDepartment of Molecular Pharmacology and Physiology, University of South Florida Morsani College of Medicine, Bruce B. Downs Blvd, MDC 8, Tampa, FL, 33612, USA.
Cemre KayisliDepartment of Molecular Pharmacology and Physiology, University of South Florida Morsani College of Medicine, Bruce B. Downs Blvd, MDC 8, Tampa, FL, 33612, USA.
Yao YaoDepartment of Molecular Pharmacology and Physiology, University of South Florida Morsani College of Medicine, Bruce B. Downs Blvd, MDC 8, Tampa, FL, 33612, USA.
Mack H WuDepartment of Surgery, University of South Florida Morsani College of Medicine, 12901 Bruce B. Downs Blvd, MDC 16, Tampa, FL, 33612, USA. mwu1@usf.edu.
Sarah Y YuanDepartment of Molecular Pharmacology and Physiology, University of South Florida Morsani College of Medicine, Bruce B. Downs Blvd, MDC 8, Tampa, FL, 33612, USA. syuan@usf.edu.

Funding

Endothelial glycocalyx shedding in septic injuryR01GM142110 · NIGMS · UNIVERSITY OF SOUTH FLORIDA · 2023 to 2025
$1.4M
Vascular Barrier Leakage in InflammationR35HL150732 · UNIVERSITY OF SOUTH FLORIDA · 2025 to 2025
$894k
Extracellular Histones in Burn-induced Microvascular HyperpermeabilityR01GM143138 · UNIVERSITY OF SOUTH FLORIDA · 2025 to 2025
$331k
BLRD VA IK6 BX004210National Institute of Health, United States GM143138National Institute of Health, United States HL150732; GM142110NHLBI NIH HHS R35 HL150732NIGMS NIH HHS R01 GM142110NIGMS NIH HHS R01 GM143138U.S. Department of Veterans Affairs IK6BX004210
6 · The paper itself

Abstract

Extracellular vesicles (EVs) are potent mediators in cell-cell communication that regulate diverse cell functions through the delivery of their bioactive cargo molecules to recipient cells. Previous work from our group demonstrated elevated plasma EV levels in patients and animals following septic or inflammatory insults, with a substantial proportion originating from neutrophils. As frontline defenders against bacterial infection, activated neutrophils release germicidal factors, some of which circulate systemically and inflict collateral tissue damage at a distance, including the brain. The role of neutrophil-derived EVs in regulating blood-brain barrier (BBB) structure and permeability after septic injury remains poorly defined. In this study, we first characterized EV production by mouse neutrophils stimulated with bacterial lipopolysaccharide (LPS) and subsequently investigated their functional and mechanistic effects on BBB integrity under in vivo and in vitro settings. Nanoparticle tracking analysis (NTA), immunoblotting, and transmission electron microscopy (TEM) revealed that LPS stimulation of neutrophils promoted EV secretion, indicated by increased particle number and protein content. Systemic administration of these EVs in mice induced cerebral microvascular leakage of plasma tracers (sodium fluorescein, at 376-Da; and dextran at 3-kDa) as quantified by near-infrared (NIR) nano-imaging and fluorometric assays. In cultured brain microvascular endothelial monolayers, EVs from naïve unstimulated neutrophils exerted minimal effects, whereas EVs from LPS-stimulated neutrophils caused a concentration-dependent reduction in transendothelial electrical resistance (TER) and a significant increase in solute permeability, indicative of paracellular hyperpermeability. Confocal microscopy revealed that tight junction proteins claudin-5 and zonula occludens-1 (ZO-1), which normally form continuous belt-like structures at endothelial cell–cell contacts, appeared discontinuous or fragmented upon EV internalization. Consistently, endothelial cells exposed to activated neutrophil-derived EVs exhibited reduced expression of tight junction proteins. Furthermore, TEM of brain capillaries from EV-injected mice provided ultrastructural evidence of tight junction disruption. Collectively, these findings suggest that neutrophil activation in response to infection promotes BBB leakage through the release of EVs capable of compromising endothelial tight junction integrity.

Indexed as

Blood-Brain BarrierCapillary PermeabilityExtracellular VesiclesNeutrophilsTight JunctionsAnimalsEndothelial CellsLipopolysaccharidesMaleMiceMice, Inbred C57BLLipopolysaccharidesBlood-brain barrierClaudin-5Endothelial permeabilityExtracellular vesiclesInflammationSepsisTight junctions

Identifiers

PMID41353187
PMCPMC12797409

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.