Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 1075
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3195
Function: GetPubMedArticleOutput_2016
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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Biophysical in nature signals, due to their simplicity in implementation, are at the forefront of research and innovation to control tendon cell function in vitro. In this work, we first assessed the influence of substrate rigidity and surface topography on human tendon cells using differentially crosslinked planar and grooved collagen scaffolds. We identified the 0.5 mM 4-arm polyethylene glycol succinimidyl glutarate concentration as the optimal one to maintain basic cell function. All crosslinked grooved substrates induced bidirectional cell and synthesised matrix orientation, without bringing about a noteworthy change in gene expression. We subsequently subjected the 0.5 mM 4-arm polyethylene glycol succinimidyl glutarate crosslinked planar and grooved collagen scaffolds to no tension, static tension and cyclic tension. Basic cell function, protein synthesis and gene expression analyses experimentation identified the static tension to have beneficial effects in human tendon cell function. Collectively, this study advocates the use of combined biophysical cues to maintain physiological cell function.
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http://dx.doi.org/10.1016/j.bioadv.2025.214483 | DOI Listing |