TY - JOUR
T1 - Extracellular Vesicles From Microalgae
T2 - Uptake Studies in Human Cells and Caenorhabditis elegans
AU - Picciotto, Sabrina
AU - Santonicola, Pamela
AU - Paterna, Angela
AU - Rao, Estella
AU - Raccosta, Samuele
AU - Romancino, Daniele Paolo
AU - Noto, Rosina
AU - Touzet, Nicolas
AU - Manno, Mauro
AU - Di Schiavi, Elia
AU - Bongiovanni, Antonella
AU - Adamo, Giorgia
N1 - Publisher Copyright:
Copyright © 2022 Picciotto, Santonicola, Paterna, Rao, Raccosta, Romancino, Noto, Touzet, Manno, Di Schiavi, Bongiovanni and Adamo.
PY - 2022/3/24
Y1 - 2022/3/24
N2 - Extracellular vesicles (EVs) are lipid membrane nano-sized vesicles secreted by various cell types for intercellular communication, found in all kingdoms of life. Nanoalgosomes are a subtype of EVs derived from microalgae with a sustainable biotechnological potential. To explore the uptake, distribution and persistence of nanoalgosomes in cells and living organisms, we separated them from a culture of the chlorophyte Tetraselmis chuii cells by tangential flow filtration (TFF), labelled them with different lipophilic dyes and characterized their biophysical attributes. Then we studied the cellular uptake of labelled nanoalgosomes in human cells and in C. elegans, demonstrating that they enter the cells through an energy dependent mechanism and are localized in the cytoplasm of specific cells, where they persist for days. Our data confirm that nanoalgosomes are actively uptaken in vitro by human cells and in vivo by C. elegans cells, supporting their exploitation as potential nanocarriers of bioactive compounds for theranostic applications.
AB - Extracellular vesicles (EVs) are lipid membrane nano-sized vesicles secreted by various cell types for intercellular communication, found in all kingdoms of life. Nanoalgosomes are a subtype of EVs derived from microalgae with a sustainable biotechnological potential. To explore the uptake, distribution and persistence of nanoalgosomes in cells and living organisms, we separated them from a culture of the chlorophyte Tetraselmis chuii cells by tangential flow filtration (TFF), labelled them with different lipophilic dyes and characterized their biophysical attributes. Then we studied the cellular uptake of labelled nanoalgosomes in human cells and in C. elegans, demonstrating that they enter the cells through an energy dependent mechanism and are localized in the cytoplasm of specific cells, where they persist for days. Our data confirm that nanoalgosomes are actively uptaken in vitro by human cells and in vivo by C. elegans cells, supporting their exploitation as potential nanocarriers of bioactive compounds for theranostic applications.
KW - Caenorhabditis elegans
KW - cellular uptake
KW - extracellular vesicles
KW - microalgae
KW - nanoalgosomes
UR - http://www.scopus.com/inward/record.url?scp=85128219558&partnerID=8YFLogxK
U2 - 10.3389/fbioe.2022.830189
DO - 10.3389/fbioe.2022.830189
M3 - Article
AN - SCOPUS:85128219558
SN - 2296-4185
VL - 10
JO - Frontiers in Bioengineering and Biotechnology
JF - Frontiers in Bioengineering and Biotechnology
M1 - 830189
ER -