Tibullo Daniele, Di Rosa Michelino, Giallongo Cesarina, La Cava Piera, Parrinello Nunziatina L, Romano Alessandra, Conticello Concetta, Brundo Maria V, Saccone Salvatore, Malaguarnera Lucia, Di Raimondo Francesco
Section of Hematology, Department of Surgery and Medical Specialties, University of Catania , Catania, Italy.
Department of Biomedical and Biotechnology Sciences, University of Catania , Catania, Italy.
Front Pharmacol. 2015 Oct 14;6:226. doi: 10.3389/fphar.2015.00226. eCollection 2015.
Osteolytic bone disease is a common manifestation of multiple myeloma (MM) that leads to progressive skeleton destruction and is the most severe cause of morbidity in MM patients. It results from increased osteolytic activity and decrease osteoblastic function. Activation of mammalian chitinases chitotriosidase (CHIT1) and YKL40 is associated with osteoclast (OCs) differentiation and bone digestion. In the current study, we investigated the effect of two Bortezomib's concentration (2.5 and 5 nM) on osteoclastogenesis by analyzing regulation of chitinase expression. OCs exposition to bortezomib (BO) was able to inhibit the expression of different OCs markers such as RANK, CTSK, TRAP, and MMP9. In addition BO-treatment reduced CHIT1 enzymatic activity and both CHIT1 and YKL40 mRNA expression levels and cytoplasmatic and secreted protein. Moreover, immunofluorescence evaluation of mature OCs showed that BO was able to translocate YKL40 into the nucleus, while CHIT1 remained into the cytoplasm. Since MM cell lines such as U266, SKM-M1 and MM1 showed high levels of CHIT1 activity, we analyzed bone resorption ability of U266 using dentin disk assay resorption pits. Silencing chitinase proteins in U266 cell line with specific small interfering RNA, resulted in pits number reduction on dentine disks. In conclusion, we showed that BO decreases osteoclastogenesis and reduces bone resorption in OCs and U266 cell line by modulating the chitinases CHIT1 and YKL40. These results indicate that chitinases may be a therapeutic target for bone disease in MM patients.
溶骨性骨病是多发性骨髓瘤(MM)的常见表现,可导致进行性骨骼破坏,是MM患者发病的最严重原因。它是由溶骨活性增加和成骨功能降低引起的。哺乳动物几丁质酶壳三糖苷酶(CHIT1)和YKL40的激活与破骨细胞(OCs)分化和骨消化有关。在本研究中,我们通过分析几丁质酶表达的调节,研究了两种硼替佐米浓度(2.5和5 nM)对破骨细胞生成的影响。OCs暴露于硼替佐米(BO)能够抑制不同OCs标志物如RANK、CTSK、TRAP和MMP9的表达。此外,BO处理降低了CHIT1酶活性以及CHIT1和YKL40的mRNA表达水平以及细胞质和分泌蛋白。此外,对成熟OCs的免疫荧光评估表明,BO能够将YKL40转运到细胞核中,而CHIT1则保留在细胞质中。由于U266、SKM-M1和MM1等MM细胞系显示出高水平的CHIT1活性,我们使用牙本质盘吸收凹坑分析了U266的骨吸收能力。用特异性小干扰RNA沉默U266细胞系中的几丁质酶蛋白,导致牙本质盘上的凹坑数量减少。总之,我们表明BO通过调节几丁质酶CHIT1和YKL40降低了OCs和U266细胞系中的破骨细胞生成并减少了骨吸收。这些结果表明,几丁质酶可能是MM患者骨病的治疗靶点。