Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
Function: GetPubMedArticleOutput_2016
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Exosomes are small endosome-derived extracellular vesicles that participate in cell-cell communication, particularly in the context of tumorigenesis, and their secretion is influenced by the tumor microenvironment. While previous studies suggest that mechanical forces may enhance exosome release, the direct relationship between these forces and exosome secretion needs to be further characterized. Here, we utilized dual-color CD63 reporter-based high-speed live-cell imaging to visualize how mechanical forces influence exosome release in situ. Through live-cell tracking, we observed the dynamic fusion of multivesicular bodies (MVBs) with the plasma membrane (PM) to release exosomes at the single-vesicle level. More importantly, we directly detected a real-time stimulatory effect of mechanical forces on exosome release, with a bulk release of exosomes occurring under mechanical pressure stimulation. Furthermore, we identified mechanical force-induced actin rearrangement as a crucial determinant of exosome release. Our findings provide direct insights into the role of mechanical forces in exosome release and lay the groundwork for developing potential strategies to target disease-derived exosomes from their source.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1021/acs.analchem.4c04690 | DOI Listing |
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