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
In the periodontal ligament (PDL) of normal rat molars, a considerable number of dendritic cells (DCs) are distributed as resident immunocompetent cells. We have hypothesized that the resident type of DCs can alter their morphology and phenotype to adapt to the microenvironment of the PDL. Thus, we have compared the characteristics of DCs in various regions of rat PDL by immunoelectron microscopy and gene expression analysis by means of reverse transcription/polymerase chain reaction. DCs in the periapical region show immature characteristics, i.e., small round profiles and few organelles. In the mesial region, which is the most stable area in the PDL, the density of DCs is the highest. DCs in the furcal region show the characteristics of activated antigen-presenting cells, i.e., CD86(high) expression, electron-dense lysosomes, and cell-to-cell contacts with lymphocytes. When the PDL is bacterially challenged by pulp exposure, the number of CD86+ DCs and contacts with lymphocytes increase in the furcal region. Gene expression analysis for the furcal region has also shown the up-regulation of the major histocompatibility complex class II alpha-chain, CD83, CD86, and the antigen-presenting cell-lectin-like receptor A1. Thus, we have demonstrated heterogeneity in resident DCs. This may be associated with the difference in DCs regarding their state of maturation/activation, which may further reflect microenvironmental differences such as the amount of external antigens.
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Source |
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http://dx.doi.org/10.1007/s00441-007-0539-7 | DOI Listing |
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