Extracellular Vesicles Tropism: A Comparative Study between Passive Innate Tropism and the Active Engineered Targeting Capability of Lymphocyte-Derived EVs
Cellular communications take place thanks to a well-connected network of chemical–physical signals, biomolecules, growth factors, and vesicular messengers that travel inside or between cells. A deep knowledge of the extracellular vesicle (EV) system allows for a better understanding of the whole ser...
Guardado en:
Autores principales: | , , , , , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
MDPI AG
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/c54ee43f9ffd4030b0e03cb3f897e15a |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:c54ee43f9ffd4030b0e03cb3f897e15a |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:c54ee43f9ffd4030b0e03cb3f897e15a2021-11-25T18:20:04ZExtracellular Vesicles Tropism: A Comparative Study between Passive Innate Tropism and the Active Engineered Targeting Capability of Lymphocyte-Derived EVs10.3390/membranes111108862077-0375https://doaj.org/article/c54ee43f9ffd4030b0e03cb3f897e15a2021-11-01T00:00:00Zhttps://www.mdpi.com/2077-0375/11/11/886https://doaj.org/toc/2077-0375Cellular communications take place thanks to a well-connected network of chemical–physical signals, biomolecules, growth factors, and vesicular messengers that travel inside or between cells. A deep knowledge of the extracellular vesicle (EV) system allows for a better understanding of the whole series of phenomena responsible for cell proliferation and death. To this purpose, here, a thorough immuno-phenotypic characterization of B-cell EV membranes is presented. Furthermore, the cellular membrane of B lymphocytes, Burkitt lymphoma, and human myeloid leukemic cells were characterized through cytofluorimetry assays and fluorescent microscopy analysis. Through cytotoxicity and internalization tests, the tropism of B lymphocyte-derived EVs was investigated toward the parental cell line and two different cancer cell lines. In this study, an innate capability of passive targeting of the native EVs was distinguished from the active targeting capability of monoclonal antibody-engineered EVs, able to selectively drive the vesicles, enhancing their internalization into the target cancer cells. In particular, the specific targeting ability of anti-CD20 engineered EVs towards Daudi cells, highly expressing CD20 marker on their cell membrane, was proved, while almost no internalization events were observed in HL60 cells, since they did not express an appreciable amount of the CD20 marker on their plasma membranes.Tania LimongiFrancesca SusaBianca DumontelLuisa RaccaMichela Perrone DonnorsoDoriana DebellisValentina CaudaMDPI AGarticleextracellular vesiclesB lymphocyteshuman myeloid leukemiaBurkitt lymphomasurface labelingcellular uptakeChemical technologyTP1-1185Chemical engineeringTP155-156ENMembranes, Vol 11, Iss 886, p 886 (2021) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
extracellular vesicles B lymphocytes human myeloid leukemia Burkitt lymphoma surface labeling cellular uptake Chemical technology TP1-1185 Chemical engineering TP155-156 |
spellingShingle |
extracellular vesicles B lymphocytes human myeloid leukemia Burkitt lymphoma surface labeling cellular uptake Chemical technology TP1-1185 Chemical engineering TP155-156 Tania Limongi Francesca Susa Bianca Dumontel Luisa Racca Michela Perrone Donnorso Doriana Debellis Valentina Cauda Extracellular Vesicles Tropism: A Comparative Study between Passive Innate Tropism and the Active Engineered Targeting Capability of Lymphocyte-Derived EVs |
description |
Cellular communications take place thanks to a well-connected network of chemical–physical signals, biomolecules, growth factors, and vesicular messengers that travel inside or between cells. A deep knowledge of the extracellular vesicle (EV) system allows for a better understanding of the whole series of phenomena responsible for cell proliferation and death. To this purpose, here, a thorough immuno-phenotypic characterization of B-cell EV membranes is presented. Furthermore, the cellular membrane of B lymphocytes, Burkitt lymphoma, and human myeloid leukemic cells were characterized through cytofluorimetry assays and fluorescent microscopy analysis. Through cytotoxicity and internalization tests, the tropism of B lymphocyte-derived EVs was investigated toward the parental cell line and two different cancer cell lines. In this study, an innate capability of passive targeting of the native EVs was distinguished from the active targeting capability of monoclonal antibody-engineered EVs, able to selectively drive the vesicles, enhancing their internalization into the target cancer cells. In particular, the specific targeting ability of anti-CD20 engineered EVs towards Daudi cells, highly expressing CD20 marker on their cell membrane, was proved, while almost no internalization events were observed in HL60 cells, since they did not express an appreciable amount of the CD20 marker on their plasma membranes. |
format |
article |
author |
Tania Limongi Francesca Susa Bianca Dumontel Luisa Racca Michela Perrone Donnorso Doriana Debellis Valentina Cauda |
author_facet |
Tania Limongi Francesca Susa Bianca Dumontel Luisa Racca Michela Perrone Donnorso Doriana Debellis Valentina Cauda |
author_sort |
Tania Limongi |
title |
Extracellular Vesicles Tropism: A Comparative Study between Passive Innate Tropism and the Active Engineered Targeting Capability of Lymphocyte-Derived EVs |
title_short |
Extracellular Vesicles Tropism: A Comparative Study between Passive Innate Tropism and the Active Engineered Targeting Capability of Lymphocyte-Derived EVs |
title_full |
Extracellular Vesicles Tropism: A Comparative Study between Passive Innate Tropism and the Active Engineered Targeting Capability of Lymphocyte-Derived EVs |
title_fullStr |
Extracellular Vesicles Tropism: A Comparative Study between Passive Innate Tropism and the Active Engineered Targeting Capability of Lymphocyte-Derived EVs |
title_full_unstemmed |
Extracellular Vesicles Tropism: A Comparative Study between Passive Innate Tropism and the Active Engineered Targeting Capability of Lymphocyte-Derived EVs |
title_sort |
extracellular vesicles tropism: a comparative study between passive innate tropism and the active engineered targeting capability of lymphocyte-derived evs |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/c54ee43f9ffd4030b0e03cb3f897e15a |
work_keys_str_mv |
AT tanialimongi extracellularvesiclestropismacomparativestudybetweenpassiveinnatetropismandtheactiveengineeredtargetingcapabilityoflymphocytederivedevs AT francescasusa extracellularvesiclestropismacomparativestudybetweenpassiveinnatetropismandtheactiveengineeredtargetingcapabilityoflymphocytederivedevs AT biancadumontel extracellularvesiclestropismacomparativestudybetweenpassiveinnatetropismandtheactiveengineeredtargetingcapabilityoflymphocytederivedevs AT luisaracca extracellularvesiclestropismacomparativestudybetweenpassiveinnatetropismandtheactiveengineeredtargetingcapabilityoflymphocytederivedevs AT michelaperronedonnorso extracellularvesiclestropismacomparativestudybetweenpassiveinnatetropismandtheactiveengineeredtargetingcapabilityoflymphocytederivedevs AT dorianadebellis extracellularvesiclestropismacomparativestudybetweenpassiveinnatetropismandtheactiveengineeredtargetingcapabilityoflymphocytederivedevs AT valentinacauda extracellularvesiclestropismacomparativestudybetweenpassiveinnatetropismandtheactiveengineeredtargetingcapabilityoflymphocytederivedevs |
_version_ |
1718411345578164224 |