Determination of chitinases family during osteoclastogenesis

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• 作者：Michelino Di Rosa^a ; ^{chitotriosidase@gmail.com" class="auth_mail} ; ^{mdirosa@unict.it" class="auth_mail} ; Daniele Tibullo^b ; Michele Vecchio^d ; Giuseppe Nunnari^c ; Salvatore Saccone^e ; Francesco Di Raimondo^b ; Lucia Malaguarnera^a
• 关键词：CHIT1 ; chitotriosidase ; CHI3L1 ; chitinase 3-like-1 ; MMP9 ; matrix metallopeptidase 9 ; siRNA ; small interfering RNA ; CPhoDs ; calcium phosphate thin film discs ; DDs ; dentin discs
• 刊名：Bone
• 出版年：April, 2014
• 年：2014
• 卷：61
• 期：Complete
• 页码：55-63
• 全文大小：1303 K

文摘

Mammalian chitinases consisting of CHIA, CHIT1, CHI3L1, CHI3L2 and CHID1 exert important biological roles in the monocyte lineage and chronic inflammatory diseases. Pathological bone resorption is a cause of significant morbidity in diseases affecting the skeleton such as rheumatoid arthritis, osteoporosis, periodontitis and cancer metastasis. The biologic role of chitinases in bone resorption is poorly understood. In this study, we evaluated the expression of the chitinases family during osteoclast differentiation. The expression of CHIA, CHI3L2 and CHID1 resulted unchanged during osteoclast differentiation, whereas CHIT1 and CHI3L1 increased significantly. We also observed that CHIT1 and CHI3L1 are involved in osteoclast function. Indeed, silencing CHIT1 and CHI3L1 with siRNA resulted in a significant decrease in bone resorption activity. In addition, transfection with CHIT1 or CHI3L1 siRNA and co-transfection with both decreased the levels of the pro-differentiative marker MMP9. Overall, these discoveries reveal a novel and crucial role for both CHIT1 and CHI3L1 in promoting bone resorption and identifying new potential candidate markers for therapeutic targeting.