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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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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