Association between an Increased Serum CCL5 Level and Pathophysiology of Degenerative Joint Disease in the Temporomandibular Joint in Females

被引:3
|
作者
Watanabe, Haruhisa [1 ,2 ]
Iori, Takashi [1 ,2 ]
Lee, Ji-Won [2 ]
Kajii, Takashi S. S. [2 ,3 ]
Takakura, Aya [4 ]
Takao-Kawabata, Ryoko [4 ]
Kitagawa, Yoshimasa [1 ]
Maruoka, Yutaka [2 ,5 ]
Iimura, Tadahiro [2 ]
机构
[1] Hokkaido Univ, Fac & Grad Sch Dent Med, Dept Oral Diag & Med, Sapporo, Hokkaido 0608586, Japan
[2] Hokkaido Univ, Fac & Grad Sch Dent Med, Dept Pharmacol, Sapporo, Hokkaido 0608686, Japan
[3] Keiyu Kai Sapporo Hosp, Dept Orthodont, Sapporo, Hokkaido 0600061, Japan
[4] Asahi Kasei Pharm Corp, Pharmaceut Res Ctr, Izunokini 4102321, Japan
[5] Ctr Hosp, Natl Ctr Global Hlth & Med, Dept Oral Surg, Tokyo 1628655, Japan
基金
日本科学技术振兴机构; 日本学术振兴会;
关键词
CCL5; temporomandibular joint; degenerative joint disease; mandible; joint; bone metabolism; osteoarthritis; CONDYLAR RESORPTION; DISC DISPLACEMENT; CYTOKINE LEVELS; BONE LOSS; DISORDERS; CHEMOKINE; CARTILAGE; ESTROGEN; OSTEOARTHRITIS; INFLAMMATION;
D O I
10.3390/ijms24032775
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Degenerative joint disease of the temporomandibular joints (DJD-TMJ) clinically manifests with symptoms such as orofacial pain, joint sounds and limited jaw movements. Our research group previously reported the functional necessity of a chemokine-chemokine receptor axis of CCL5-CCR5 in osteoclasts. Accumulated studies reported that this axis was involved in the pathogenesis of bone and joint destructive diseases, suggesting CCL5 as a potent biomarker. This study investigated whether or not the serum level of CCL5 can be a biomarker of DJD-TMJ and concomitantly analyzed changes in the serum and urine levels of bone markers to see whether or not changes in the rate of bone metabolism were predisposing. We enrolled 17 female subjects with diagnosed DJD-TMJ and sexually and age-matched 17 controls. The serum CCL5 level in DJD-TMJ subjects was significantly higher than that in the control subjects. Multivariate analyses indicated an association between an augmented CCL5 level and the rate of bone metabolism, especially in relatively young DJD-TMJ subjects without other systemic symptoms. A principal component analysis of serum markers and our pharmacological experiment using a postmenopausal model of ovariectomized rats suggested that an augmented serum CCL5 level specifically reflected DJD-TMJ and that covert changes in the rate of bone metabolism predisposed individuals to DJD-TMJ.
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页数:18
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