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

Author:

Watanabe Haruhisa12,Iori Takashi12,Lee Ji-Won2,Kajii Takashi S.23,Takakura Aya4,Takao-Kawabata Ryoko4ORCID,Kitagawa Yoshimasa1,Maruoka Yutaka25,Iimura Tadahiro2ORCID

Affiliation:

1. Department of Oral Diagnosis and Medicine, Faculty and Graduate School of Dental Medicine, Hokkaido University, Sapporo 060-8586, Japan

2. Department of Pharmacology, Faculty and Graduate School of Dental Medicine, Hokkaido University, Sapporo 060-8686, Japan

3. Department of Orthodontics, Keiyu-kai Sapporo Hospital, Sapporo 060-0061, Japan

4. Pharmaceuticals Research Center, Asahi Kasei Pharma Corporation, Izunokini 410-2321, Japan

5. Department of Oral Surgery, Center Hospital, National Center for Global Health and Medicine, Tokyo 162-8655, Japan

Abstract

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.

Funder

NCGM Intramural Research Fund

Grant-in-Aid for Scientific Research

Takeda Science Foundation and the Mochida Memorial Foundation for Medical and Pharmaceutical Research

JST SPRING

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Osteoarthritis year in review 2023: metabolite and protein biomarkers;Osteoarthritis and Cartilage;2023-11

2. Bone and Cartilage Biology;International Journal of Molecular Sciences;2023-03-09

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