Expression of ADAMTS-5 in deformed human temporomandibular joint discs

To study the expression of a disintegrin and metalloproteinase with thrombospondin motifs 5 (ADAMTS-5) in tissue samples of deformed human temporomandibular joint (TMJ) discs and cells obtained from the discs. Eleven adult human TMJ discs (nine diseased discs and two normal discs) were used in this...

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Published inHistology and histopathology Vol. 23; no. 12; p. 1485
Main Authors Matsumoto, Takashi, Tojyo, Itaru, Kiga, Norifumi, Hiraishi, Yukihiro, Fujita, Shigeyuki
Format Journal Article
LanguageEnglish
Published Spain 01.12.2008
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Summary:To study the expression of a disintegrin and metalloproteinase with thrombospondin motifs 5 (ADAMTS-5) in tissue samples of deformed human temporomandibular joint (TMJ) discs and cells obtained from the discs. Eleven adult human TMJ discs (nine diseased discs and two normal discs) were used in this study. The nine diseased discs were obtained from nine patients with internal derangement (ID) and osteoarthritis (OA) in the TMJ. These patients all had anteriorly displaced discs and deformed mandibular condyles, making conservative therapy impossible. The tissues were immunohistochemically stained using ADAMTS-5 antibodies. In addition, an articular disc cell line from one case was established by collagenase treatment. The subcultured cells under both normal and hypoxic conditions (O2: 2%) were incubated for 3, 6, 12 and 24 h after addition of interleukin-1beta (IL-1beta) (1 ng/mL). Subsequently, the expression of ADAMTS-5 was examined using reverse transcription-polymerase chain reaction (RT-PCR). The control group showed negative reactions on immunohistochemical staining. The discs extracted from cases with ID and OA presented positive reactions for ADAMTS-5. The expression of ADAMTS-5 mRNA increased under both normoxia and hypoxia with the addition of IL-1beta, and the peak was observed after 3 h. These results suggest that ADAMTS-5 is related to deformation and destruction of human TMJ discs affected by ID and OA.
ISSN:1699-5848
DOI:10.14670/HH-23.1485