Ultrasound and microbubble induced release from intracellular compartments
BMC Biotechnology, ISSN: 1472-6750, Vol: 17, Issue: 1, Page: 45
2017
- 16Citations
- 58Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations16
- Citation Indexes16
- 16
- CrossRef11
- Captures58
- Readers58
- 58
Article Description
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.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85019606600&origin=inward; http://dx.doi.org/10.1186/s12896-017-0364-3; http://www.ncbi.nlm.nih.gov/pubmed/28521780; http://bmcbiotechnol.biomedcentral.com/articles/10.1186/s12896-017-0364-3; https://dx.doi.org/10.1186/s12896-017-0364-3; https://bmcbiotechnol.biomedcentral.com/articles/10.1186/s12896-017-0364-3
Springer Science and Business Media LLC
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