2016
DOI: 10.1111/jre.12370
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The histopathological comparison on the destruction of the periodontal tissue between normal junctional epithelium and long junctional epithelium

Abstract: Our findings suggest that the destruction of periodontal tissue is increased in tissue containing long junctional epithelium compared with normal junctional epithelium and that the immunized condition accelerates the destruction by forming immune complexes.

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Cited by 26 publications
(32 citation statements)
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References 32 publications
(36 reference statements)
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“…The thickness of JE was measured by counting the number of epithel layers from the cemento-enamel junction (CEJ) to the most coronal and apical sections of JE. 22 The PAS positive gland staining produced a magenta-purple colour in the duct cell. The mucin level was measured based on the density of the mucin cell expression in the submandibular gland.…”
Section: Methodsmentioning
confidence: 99%
“…The thickness of JE was measured by counting the number of epithel layers from the cemento-enamel junction (CEJ) to the most coronal and apical sections of JE. 22 The PAS positive gland staining produced a magenta-purple colour in the duct cell. The mucin level was measured based on the density of the mucin cell expression in the submandibular gland.…”
Section: Methodsmentioning
confidence: 99%
“…Blood samples (150 μL) from the retro‐orbital venous plexus of rats under general anesthesia with isoflurane were collected into microhematocrit tubes just before the first topical application (baseline) and immediately after the 5th and 10th applications. The levels of anti‐LPS IgG in serum samples of individual rats were determined by an indirect ELISA, as described previously . Ninety‐six‐well microtiter plates were coated (100 μL/well) with a 2.5 μg/mL solution of LPS from E. coli in 0.05 M carbonate buffer (pH 9.6) and incubated for 16 hours at 4°C.…”
Section: Methodsmentioning
confidence: 99%
“…Immunohistological staining of complement component C1q was performed to detect immune complexes, as described previously . After the sections were deparaffinized, endogenous peroxidase activity was blocked with 0.3% H 2 O 2 /methanol for 30 minutes, followed by incubation in normal goat serum for 30 minutes at room temperature.…”
Section: Methodsmentioning
confidence: 99%
“…Bacterial biofilm attaches to the tooth surface, making it impossible for the immune system to eradicate the infecting microorganisms efficiently, perpetuating the insult to the periodontal tissues [18]. The junctional epithelium is the first periodontal structure to face the bacterial challenge [23]. Bacteria are capable to cross the junctional epithelium and pass to the gingival conjunctive tissue, where they stimulate the gingival epithelial cells and fibroblasts to trigger the initial inflammatory responses [24].…”
Section: Innate Immune Response In Periodontal Diseasementioning
confidence: 99%