Ultrasound and microbubble induced release from intracellular compartments

Abstract Background Ultrasound and microbubbles (USMB) have been shown to enhance the intracellular uptake of molecules, generally thought to occur as a result of sonoporation. The underlying mechanism associated with USMB-enhanced intracellular uptake such as membrane disruption and endocytosis may...

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Main Authors: Farah Hussein, Costin Antonescu, Raffi Karshafian
Format: Article
Language:English
Published: BMC 2017-05-01
Series:BMC Biotechnology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12896-017-0364-3
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spelling doaj-2f77642fbe044e7f8252e9b819476ff82020-11-25T03:55:11ZengBMCBMC Biotechnology1472-67502017-05-0117111210.1186/s12896-017-0364-3Ultrasound and microbubble induced release from intracellular compartmentsFarah Hussein0Costin Antonescu1Raffi Karshafian2Department of Physics, Ryerson UniversityDepartment of Chemistry and Biology, Ryerson UniversityDepartment of Physics, Ryerson UniversityAbstract Background Ultrasound and microbubbles (USMB) have been shown to enhance the intracellular uptake of molecules, generally thought to occur as a result of sonoporation. The underlying mechanism associated with USMB-enhanced intracellular uptake such as membrane disruption and endocytosis may also be associated with USMB-induced release of cellular materials to the extracellular milieu. This study investigates USMB effects on the molecular release from cells through membrane-disruption and exocytosis. Results USMB induced the release of 19% and 67% of GFP from the cytoplasm in viable and non-viable cells, respectively. Tfn release from early/recycling endosomes increased by 23% in viable cells upon USMB treatment. In addition, the MFI of LAMP-1 antibody increased by 50% in viable cells, suggesting USMB-stimulated lysosome exocytosis. In non-viable cells, labeling of LAMP-1 intracellular structures in the absence of cell permeabilization by detergents suggests that USMB-induced cell death correlates with lysosomal permeabilization. Conclusions In conclusion, USMB enhanced the molecular release from the cytoplasm, lysosomes, and early/recycling endosomes.http://link.springer.com/article/10.1186/s12896-017-0364-3Ultrasound and microbubbleSonoporationEndocytosisExocytosisIntracellular uptakeIntracellular release
collection DOAJ
language English
format Article
sources DOAJ
author Farah Hussein
Costin Antonescu
Raffi Karshafian
spellingShingle Farah Hussein
Costin Antonescu
Raffi Karshafian
Ultrasound and microbubble induced release from intracellular compartments
BMC Biotechnology
Ultrasound and microbubble
Sonoporation
Endocytosis
Exocytosis
Intracellular uptake
Intracellular release
author_facet Farah Hussein
Costin Antonescu
Raffi Karshafian
author_sort Farah Hussein
title Ultrasound and microbubble induced release from intracellular compartments
title_short Ultrasound and microbubble induced release from intracellular compartments
title_full Ultrasound and microbubble induced release from intracellular compartments
title_fullStr Ultrasound and microbubble induced release from intracellular compartments
title_full_unstemmed Ultrasound and microbubble induced release from intracellular compartments
title_sort ultrasound and microbubble induced release from intracellular compartments
publisher BMC
series BMC Biotechnology
issn 1472-6750
publishDate 2017-05-01
description Abstract Background Ultrasound and microbubbles (USMB) have been shown to enhance the intracellular uptake of molecules, generally thought to occur as a result of sonoporation. The underlying mechanism associated with USMB-enhanced intracellular uptake such as membrane disruption and endocytosis may also be associated with USMB-induced release of cellular materials to the extracellular milieu. This study investigates USMB effects on the molecular release from cells through membrane-disruption and exocytosis. Results USMB induced the release of 19% and 67% of GFP from the cytoplasm in viable and non-viable cells, respectively. Tfn release from early/recycling endosomes increased by 23% in viable cells upon USMB treatment. In addition, the MFI of LAMP-1 antibody increased by 50% in viable cells, suggesting USMB-stimulated lysosome exocytosis. In non-viable cells, labeling of LAMP-1 intracellular structures in the absence of cell permeabilization by detergents suggests that USMB-induced cell death correlates with lysosomal permeabilization. Conclusions In conclusion, USMB enhanced the molecular release from the cytoplasm, lysosomes, and early/recycling endosomes.
topic Ultrasound and microbubble
Sonoporation
Endocytosis
Exocytosis
Intracellular uptake
Intracellular release
url http://link.springer.com/article/10.1186/s12896-017-0364-3
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