Dynamic changes of extracellular vesicles during zebrafish organogenesis

Abstract Extracellular Vesicles (EVs) play a crucial role in cell differentiation. Despite its role as a well-established vertebrate model, little is known about EVs during zebrafish embryogenesis. This study investigates EVs during zebrafish embryogenesis, analysing size- and concentration-changes...

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Main Authors: Linda-Marie Mulzer, Tim Felger, Luis E. Muñoz, Gesa Engl, Heiko Reutter, Mario Schiffer, Leila Pourtalebi Jahromi, Fanni Annamária Boros, Friederike Zunke, Philipp Arnold, Alina C. Hilger
Format: Article
Language:English
Published: BMC 2025-02-01
Series:Cell Communication and Signaling
Online Access:https://doi.org/10.1186/s12964-025-02053-x
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author Linda-Marie Mulzer
Tim Felger
Luis E. Muñoz
Gesa Engl
Heiko Reutter
Mario Schiffer
Leila Pourtalebi Jahromi
Fanni Annamária Boros
Friederike Zunke
Philipp Arnold
Alina C. Hilger
author_facet Linda-Marie Mulzer
Tim Felger
Luis E. Muñoz
Gesa Engl
Heiko Reutter
Mario Schiffer
Leila Pourtalebi Jahromi
Fanni Annamária Boros
Friederike Zunke
Philipp Arnold
Alina C. Hilger
author_sort Linda-Marie Mulzer
collection DOAJ
description Abstract Extracellular Vesicles (EVs) play a crucial role in cell differentiation. Despite its role as a well-established vertebrate model, little is known about EVs during zebrafish embryogenesis. This study investigates EVs during zebrafish embryogenesis, analysing size- and concentration-changes over time. Wild-type AB strain zebrafish larvae (zfl) were collected at 24, 48, 72, and 96 h post fertilization (hpf) and homogenized. EVs were isolated and characterized using flow cytometry, negative staining transmission electron microscopy (TEM), nanoparticle tracking analysis (NTA), and Western Blot. Flow cytometry and TEM showed a high purity of the samples. Small EVs (sEVs) and large EVs (lEVs) were differentiated using NTA, showing that zfl use different types of EVs during embryogenesis. It was observed that the total EV number increased significantly over the first 72 hpf, but not proportionally to zfl growth in length. Additionally, sEV size also increased significantly, with a maximum diameter at 72 hpf. Since most organs are formed during the first 72 hpf and from then on mainly maturation and growth occur, the elevated number and larger size before 72 hpf suggests an important role of EVs during zebrafish organogenesis. Since EVs serve as cargo delivery platforms, the increase in size of sEVs may reflect the need for a higher transport capacity.
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spelling doaj-art-ef02f347753c42809c653bad9d2199332025-02-09T12:47:19ZengBMCCell Communication and Signaling1478-811X2025-02-0123111010.1186/s12964-025-02053-xDynamic changes of extracellular vesicles during zebrafish organogenesisLinda-Marie Mulzer0Tim Felger1Luis E. Muñoz2Gesa Engl3Heiko Reutter4Mario Schiffer5Leila Pourtalebi Jahromi6Fanni Annamária Boros7Friederike Zunke8Philipp Arnold9Alina C. Hilger10Department of Pediatrics and Adolescent Medicine, Division of Neonatology and Pediatric, Intensive Care University Hospital ErlangenDepartment of Pediatrics and Adolescent Medicine, Division of Neonatology and Pediatric, Intensive Care University Hospital ErlangenDepartment of Internal Medicine 3 Rheumatology and Immunology, Friedrich-Alexander- University Erlangen-Nürnberg (FAU) and Universitätsklinikum ErlangenDepartment of Pediatrics and Adolescent Medicine, Division of Neonatology and Pediatric, Intensive Care University Hospital ErlangenDepartment of Pediatrics and Adolescent Medicine, Division of Neonatology and Pediatric, Intensive Care University Hospital ErlangenDepartment of Internal Medicine 4 Nephrology, Friedrich-Alexander-University Erlangen- Nürnberg (FAU) and Universitätsklinikum ErlangenDepartment of Biology, Friedrich-Alexander-University Erlangen (FAU)Department of Molecular Neurology, University Hospital Erlangen, Friedrich-Alexander- University Erlangen-Nürnberg (FAU)Department of Molecular Neurology, University Hospital Erlangen, Friedrich-Alexander- University Erlangen-Nürnberg (FAU)Institute of Anatomy, Functional and Clinical Anatomy, Friedrich-Alexander-University Erlangen-Nürnberg (FAU)Department of Pediatrics and Adolescent Medicine, University Hospital ErlangenAbstract Extracellular Vesicles (EVs) play a crucial role in cell differentiation. Despite its role as a well-established vertebrate model, little is known about EVs during zebrafish embryogenesis. This study investigates EVs during zebrafish embryogenesis, analysing size- and concentration-changes over time. Wild-type AB strain zebrafish larvae (zfl) were collected at 24, 48, 72, and 96 h post fertilization (hpf) and homogenized. EVs were isolated and characterized using flow cytometry, negative staining transmission electron microscopy (TEM), nanoparticle tracking analysis (NTA), and Western Blot. Flow cytometry and TEM showed a high purity of the samples. Small EVs (sEVs) and large EVs (lEVs) were differentiated using NTA, showing that zfl use different types of EVs during embryogenesis. It was observed that the total EV number increased significantly over the first 72 hpf, but not proportionally to zfl growth in length. Additionally, sEV size also increased significantly, with a maximum diameter at 72 hpf. Since most organs are formed during the first 72 hpf and from then on mainly maturation and growth occur, the elevated number and larger size before 72 hpf suggests an important role of EVs during zebrafish organogenesis. Since EVs serve as cargo delivery platforms, the increase in size of sEVs may reflect the need for a higher transport capacity.https://doi.org/10.1186/s12964-025-02053-x
spellingShingle Linda-Marie Mulzer
Tim Felger
Luis E. Muñoz
Gesa Engl
Heiko Reutter
Mario Schiffer
Leila Pourtalebi Jahromi
Fanni Annamária Boros
Friederike Zunke
Philipp Arnold
Alina C. Hilger
Dynamic changes of extracellular vesicles during zebrafish organogenesis
Cell Communication and Signaling
title Dynamic changes of extracellular vesicles during zebrafish organogenesis
title_full Dynamic changes of extracellular vesicles during zebrafish organogenesis
title_fullStr Dynamic changes of extracellular vesicles during zebrafish organogenesis
title_full_unstemmed Dynamic changes of extracellular vesicles during zebrafish organogenesis
title_short Dynamic changes of extracellular vesicles during zebrafish organogenesis
title_sort dynamic changes of extracellular vesicles during zebrafish organogenesis
url https://doi.org/10.1186/s12964-025-02053-x
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