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
Protease-activated receptor 1 (PAR) has been associated to tissue repair and bone healing. The aim of the present study was to evaluate the effect of PAR activation on the osteogenic activity of human periodontal ligament stem cells (PDLSCs). PDLSCs were cultured in the presence of PAR-selective agonist peptide (100 nM), thrombin (0.1 U/mL), or PAR antagonist peptide (100 nM). Calcium deposits, calcium concentration (supernatant), alkaline phosphatase activity (ALP), cell proliferation, and gene (qPCR) and protein expression (ELISA assay) of osteogenic factors were assessed at 2, 7, and 14 days. PAR activation led to increased calcium deposits ( < 0.05), calcium concentration ( < 0.05), ALP activity ( < 0.05), and cell proliferation ( < 0.05). Further, PAR activation may increase gene and protein expression of Runx2 ( < 0.05) and OPG ( < 0.05). In conclusion, PAR activation increases osteogenic activity of PDLSCs, providing a possible new strategy for periodontal regenerative therapies.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6589281 | PMC |
http://dx.doi.org/10.1155/2019/6857386 | DOI Listing |
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