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: 3122
Function: getPubMedXML
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
Objective: Mesenchymal-epithelial transition (MET) is an important part of kidney development. However, the role of microRNA (miRNA) in MET and the regulating mechanism is still not well known.
Materials And Methods: qRT-PCR and western blot were performed to detect the expression of miR-1 and miR-802 and related protein expression. Luciferase reporter assay and western blot were used to identify the target of miR-1 and miR-802. Confocal microscopy was used to analyze the MET process.
Results: We demonstrated that miR-1 expression was downregulated and miR-802 expression was upregulated during kidney development. And during the process, proteins levels of Wnt-4 and β-catenin changed significantly. In MDCK cells, overexpression of Wnt-4 inhibited the expression of β-catenin, and promote the MET, and overexpression of β-catenin inhibited MET. Further studies suggested that miR-1 and miR-802 regulated MET by binding to Wnt-4 and β-catenin mRNA, regulated the expression of Wnt-4 and β-catenin. In conclusion, miR-1 and miR-802 regulate MET during kidney development by regulating Wnt-4/β-catenin signaling.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895509 | PMC |
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