Time-gated Raman spectroscopy and proteomics analyses of hypoxic and normoxic renal carcinoma extracellular vesicles

Abstract Extracellular vesicles (EVs) represent a diverse group of small membrane-encapsulated particles involved in cell–cell communication, but the technologies to characterize EVs are still limited. Hypoxia is a typical condition in solid tumors, and cancer-derived EVs support tumor growth and in...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Anatoliy Samoylenko, Martin Kögler, Artem Zhyvolozhnyi, Olha Makieieva, Geneviève Bart, Sampson S. Andoh, Matthieu Roussey, Seppo J. Vainio, Jussi Hiltunen
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2021
Materias:
R
Q
Acceso en línea:https://doaj.org/article/3fada35232c74dd4979f769eff191495
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:3fada35232c74dd4979f769eff191495
record_format dspace
spelling oai:doaj.org-article:3fada35232c74dd4979f769eff1914952021-12-02T18:51:28ZTime-gated Raman spectroscopy and proteomics analyses of hypoxic and normoxic renal carcinoma extracellular vesicles10.1038/s41598-021-99004-62045-2322https://doaj.org/article/3fada35232c74dd4979f769eff1914952021-10-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-99004-6https://doaj.org/toc/2045-2322Abstract Extracellular vesicles (EVs) represent a diverse group of small membrane-encapsulated particles involved in cell–cell communication, but the technologies to characterize EVs are still limited. Hypoxia is a typical condition in solid tumors, and cancer-derived EVs support tumor growth and invasion of tissues by tumor cells. We found that exposure of renal adenocarcinoma cells to hypoxia induced EV secretion and led to notable changes in the EV protein cargo in comparison to normoxia. Proteomics analysis showed overrepresentation of proteins involved in adhesion, such as integrins, in hypoxic EV samples. We further assessed the efficacy of time-gated Raman spectroscopy (TG-RS) and surface-enhanced time-gated Raman spectroscopy (TG-SERS) to characterize EVs. While the conventional continuous wave excitation Raman spectroscopy did not provide a notable signal, prominent signals were obtained with the TG-RS that were further enhanced in the TG-SERS. The Raman signal showed characteristic changes in the amide regions due to alteration in the chemical bonds of the EV proteins. The results illustrate that the TG-RS and the TG-SERS are promising label free technologies to study cellular impact of external stimuli, such as oxygen deficiency, on EV production, as well as differences arising from distinct EV purification protocols.Anatoliy SamoylenkoMartin KöglerArtem ZhyvolozhnyiOlha MakieievaGeneviève BartSampson S. AndohMatthieu RousseySeppo J. VainioJussi HiltunenNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Anatoliy Samoylenko
Martin Kögler
Artem Zhyvolozhnyi
Olha Makieieva
Geneviève Bart
Sampson S. Andoh
Matthieu Roussey
Seppo J. Vainio
Jussi Hiltunen
Time-gated Raman spectroscopy and proteomics analyses of hypoxic and normoxic renal carcinoma extracellular vesicles
description Abstract Extracellular vesicles (EVs) represent a diverse group of small membrane-encapsulated particles involved in cell–cell communication, but the technologies to characterize EVs are still limited. Hypoxia is a typical condition in solid tumors, and cancer-derived EVs support tumor growth and invasion of tissues by tumor cells. We found that exposure of renal adenocarcinoma cells to hypoxia induced EV secretion and led to notable changes in the EV protein cargo in comparison to normoxia. Proteomics analysis showed overrepresentation of proteins involved in adhesion, such as integrins, in hypoxic EV samples. We further assessed the efficacy of time-gated Raman spectroscopy (TG-RS) and surface-enhanced time-gated Raman spectroscopy (TG-SERS) to characterize EVs. While the conventional continuous wave excitation Raman spectroscopy did not provide a notable signal, prominent signals were obtained with the TG-RS that were further enhanced in the TG-SERS. The Raman signal showed characteristic changes in the amide regions due to alteration in the chemical bonds of the EV proteins. The results illustrate that the TG-RS and the TG-SERS are promising label free technologies to study cellular impact of external stimuli, such as oxygen deficiency, on EV production, as well as differences arising from distinct EV purification protocols.
format article
author Anatoliy Samoylenko
Martin Kögler
Artem Zhyvolozhnyi
Olha Makieieva
Geneviève Bart
Sampson S. Andoh
Matthieu Roussey
Seppo J. Vainio
Jussi Hiltunen
author_facet Anatoliy Samoylenko
Martin Kögler
Artem Zhyvolozhnyi
Olha Makieieva
Geneviève Bart
Sampson S. Andoh
Matthieu Roussey
Seppo J. Vainio
Jussi Hiltunen
author_sort Anatoliy Samoylenko
title Time-gated Raman spectroscopy and proteomics analyses of hypoxic and normoxic renal carcinoma extracellular vesicles
title_short Time-gated Raman spectroscopy and proteomics analyses of hypoxic and normoxic renal carcinoma extracellular vesicles
title_full Time-gated Raman spectroscopy and proteomics analyses of hypoxic and normoxic renal carcinoma extracellular vesicles
title_fullStr Time-gated Raman spectroscopy and proteomics analyses of hypoxic and normoxic renal carcinoma extracellular vesicles
title_full_unstemmed Time-gated Raman spectroscopy and proteomics analyses of hypoxic and normoxic renal carcinoma extracellular vesicles
title_sort time-gated raman spectroscopy and proteomics analyses of hypoxic and normoxic renal carcinoma extracellular vesicles
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/3fada35232c74dd4979f769eff191495
work_keys_str_mv AT anatoliysamoylenko timegatedramanspectroscopyandproteomicsanalysesofhypoxicandnormoxicrenalcarcinomaextracellularvesicles
AT martinkogler timegatedramanspectroscopyandproteomicsanalysesofhypoxicandnormoxicrenalcarcinomaextracellularvesicles
AT artemzhyvolozhnyi timegatedramanspectroscopyandproteomicsanalysesofhypoxicandnormoxicrenalcarcinomaextracellularvesicles
AT olhamakieieva timegatedramanspectroscopyandproteomicsanalysesofhypoxicandnormoxicrenalcarcinomaextracellularvesicles
AT genevievebart timegatedramanspectroscopyandproteomicsanalysesofhypoxicandnormoxicrenalcarcinomaextracellularvesicles
AT sampsonsandoh timegatedramanspectroscopyandproteomicsanalysesofhypoxicandnormoxicrenalcarcinomaextracellularvesicles
AT matthieuroussey timegatedramanspectroscopyandproteomicsanalysesofhypoxicandnormoxicrenalcarcinomaextracellularvesicles
AT seppojvainio timegatedramanspectroscopyandproteomicsanalysesofhypoxicandnormoxicrenalcarcinomaextracellularvesicles
AT jussihiltunen timegatedramanspectroscopyandproteomicsanalysesofhypoxicandnormoxicrenalcarcinomaextracellularvesicles
_version_ 1718377379977494528