Extracellular vesicle-mediated trafficking of molecular cues during human brain development

Cellular crosstalk is an essential process influenced by numerous factors, including secreted vesicles that transfer nucleic acids, lipids, and proteins between cells. Extracellular vesicles (EVs) have been the center of many studies focusing on neurodegenerative disorders, but whether EVs display cell-type-specific features for cellular crosstalk during neurodevelopment is unknown. Here, using human-induced pluripotent stem cell-derived cerebral organoids, neural progenitors, neurons, and astrocytes, we identify heterogeneity in EV protein content and dynamics in a cell-type-specific and time-dependent manner. Our results support the trafficking of key molecules via EVs in neurodevelopment, such as the transcription factor YAP1, and their localization to differing cell compartments depending on the EV recipient cell type. This study sheds new light on the biology of EVs during human brain development.

Authors

Institutions

Publication Details

Journal
Cell Reports
Published
2024-09-19
DOI
https://doi.org/10.1016/j.celrep.2024.114755
Citations
19
Primary Topic
Extracellular vesicles in disease
Type
article
Field-Weighted Citation Impact
4.44

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Extracellular vesicle-mediated trafficking of molecular cues during human brain development

Mariano Gonzalez Pisfil, Pavel Kielkowski, Natalia Baumann, Michael W. Pfaffl et al.
19 citations
Cell Reports
Extracellular vesicles in disease
4.44
article

Extracellular vesicle-mediated trafficking of molecular cues during human brain development

Mariano Gonzalez Pisfil, Pavel Kielkowski, Natalia Baumann, Michael W. Pfaffl, Benno Pütz, Sylvain Moser, Rossella Di Giaimo, Filippo M. Cernilogar, Andrea Carolina Pérez Forero, Fabrizia Pipicelli, Silvia Cappello, Christian Grätz, Giuseppina Maccarrone
article en
19 citations

Abstract

Cellular crosstalk is an essential process influenced by numerous factors, including secreted vesicles that transfer nucleic acids, lipids, and proteins between cells. Extracellular vesicles (EVs) have been the center of many studies focusing on neurodegenerative disorders, but whether EVs display cell-type-specific features for cellular crosstalk during neurodevelopment is unknown. Here, using human-induced pluripotent stem cell-derived cerebral organoids, neural progenitors, neurons, and astrocytes, we identify heterogeneity in EV protein content and dynamics in a cell-type-specific and time-dependent manner. Our results support the trafficking of key molecules via EVs in neurodevelopment, such as the transcription factor YAP1, and their localization to differing cell compartments depending on the EV recipient cell type. This study sheds new light on the biology of EVs during human brain development.

Cell ReportsVol. 43(10)
University of Geneva (CH), Centre of Experimental Medicine of the Slovak Academy of Sciences (SK), Max Planck Institute of Psychiatry (DE), Technical University of Munich (DE), Ludwig-Maximilians-Universität München (DE)
E-Rare, European Commission, Deutsche Forschungsgemeinschaft, Fritz Thyssen Stiftung, Ludwig-Maximilians-Universität München, Ministero degli Affari Esteri e della Cooperazione Internazionale
Gender equality
Openalex Percentile: Top 5%
Extracellular vesicles in disease
4.44
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.