Evidence map›Paper›PMID 37300778›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2023

Live-Imaging Detection of Multivesicular Body-Plasma Membrane Fusion and Exosome Release in Cultured Primary Neurons.

Matthew F Pescosolido, Qing Ouyang, Judy S Liu, Eric M Morrow

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. 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

4 authors at 3 institutions in 2 countries.

Matthew F PescosolidoDepartment of Molecular Biology, Cell Biology and Biochemistry; and Carney Institute for Brain Science, Brown University, Laboratories for Molecular Medicine, Providence, RI, USA.
Qing OuyangDepartment of Molecular Biology, Cell Biology and Biochemistry; and Carney Institute for Brain Science, Brown University, Laboratories for Molecular Medicine, Providence, RI, USA.
Judy S LiuDepartment of Molecular Biology, Cell Biology and Biochemistry; and Carney Institute for Brain Science, Brown University, Laboratories for Molecular Medicine, Providence, RI, USA.
Eric M MorrowDepartment of Molecular Biology, Cell Biology and Biochemistry; and Carney Institute for Brain Science, Brown University, Laboratories for Molecular Medicine, Providence, RI, USA. eric_morrow@brown.edu.
Allen Institute for Brain Science · USInstitute of Molecular and Cell Biology · RURhode Island Hospital · US

Funding

Pathogenic Mechanisms in Christianson Syndrome and NHE6-Related DisordersR01NS113141 · NINDS · BROWN UNIVERSITY · PI Eric M Morrow · 2019 to 2026
$7.0M
Mechanisms of Disease and Treatments in Novel Metabolic Development Brain DisordersR01NS121618 · NINDS · BROWN UNIVERSITY · PI Eric M Morrow · 2022 to 2026
$3.2M
Endo-lysosomal mechanisms and treatment in atypical cerebellar neurodevelopmentF31NS093880 · NINDS · BROWN UNIVERSITY · PI PESCOSOLIDO, MATTHEW F. · 2016 to 2017
$88k
NINDS NIH HHS F31 NS093880NINDS NIH HHS R01 NS113141NINDS NIH HHS R01 NS121618
6 · The paper itself

Abstract

Exosomes represent a class of extracellular vesicles (EVs) derived from the endocytic pathway that is important for cell-cell communication and implicated in the spread of pathogenic protein aggregates associated with neurological diseases. Exosomes are released extracellularly when multivesicular bodies (also known as late endosomes) fuse with the plasma membrane (PM). An important breakthrough in exosome research is the ability to capture MVB-PM fusion and exosome release simultaneously in individual cells using live-imaging microscopy techniques. Specifically, researchers have created a construct fusing CD63, a tetraspanin enriched in exosomes, with the pH-sensitive reporter pHluorin whereby CD63-pHluorin fluorescence is quenched in the acidic MVB lumen and only fluoresces when released into the less acidic extracellular environment. Here, we describe a method using this CD63-pHluorin construct to visualize MVB-PM fusion/exosome secretion in primary neurons using total internal reflection fluorescence (TIRF) microscopy.

Indexed as

ExosomesCell CommunicationMembrane FusionMultivesicular BodiesNeuronsEndocytic pathwayExosomesExtracellular vesicles (EVs)Multivesicular bodies (MVBs)Primary neuronal cultureTotal internal reflection fluorescence (TIRF)

Identifiers

PMID37300778
OpenAlexW4380187925

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.