Chairani Elissa, Fuchigami Takao, Koyama Hirofumi, Ono Yusuke, Iijima Mikio, Kishida Michiko, Kibe Toshiro, Nakamura Norifumi, Kishida Shosei
Department of Biochemistry and Genetics, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.
Department of Oral and Maxillofacial Surgery, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.
Biochem Biophys Rep. 2022 Feb 18;30:101233. doi: 10.1016/j.bbrep.2022.101233. eCollection 2022 Jul.
Ameloblastoma is an odontogenic tumor located in the bone jaw with clinical characteristics of extensive bone resorption. It is a locally invasive tumor with a high recurrence rate despite adequate surgical removal. In bone disease, tumors and other cells including osteoblasts, osteoclasts, and osteocytes in the bone microenvironment contribute to the pathogenesis of tumor growth. However, the effect of osteoblasts on ameloblastoma cells is not well-understood, and there has been limited research on interactions between them. This study investigated interactions between ameloblastoma cells and osteoblasts using a human ameloblastoma cell line (AM-3 ameloblastoma cells) and a murine pre-osteoblast cell line (MC3T3-E1 cells). We treated each cell type with the conditioned medium by the other cell type. We analyzed the effect on cytokine production by MC3T3-E1 cells and the production of MMPs by AM-3 cells. Treatment with AM-3-conditioned medium induced inflammatory cytokine production of IL-6, MCP-1, and RANTES from MC3T3-E1 cells. The use of an IL-1 receptor antagonist suppressed the production of these inflammatory cytokines by MC3T3-E1 cells stimulated with AM-3-conditioned medium. The MC3T3-E1-conditioned medium triggered the expression of MMP-2 from AM-3 cells. Furthermore, we have shown that the proliferation and migration activity of AM-3 cells were accelerated by MC3T3-E1 conditioned media. In conclusion, these intercellular signalings between ameloblastoma cells and osteoblasts may play multiple roles in the pathogenesis of ameloblastoma.
成釉细胞瘤是一种位于颌骨的牙源性肿瘤,具有广泛骨质吸收的临床特征。它是一种局部侵袭性肿瘤,尽管手术切除充分,但复发率很高。在骨疾病中,骨微环境中的肿瘤及其他细胞,包括成骨细胞、破骨细胞和骨细胞,都参与肿瘤生长的发病机制。然而,成骨细胞对成釉细胞瘤细胞的影响尚未完全了解,关于它们之间相互作用的研究也很有限。本研究使用人成釉细胞瘤细胞系(AM-3成釉细胞瘤细胞)和小鼠前成骨细胞系(MC3T3-E1细胞)来研究成釉细胞瘤细胞与成骨细胞之间的相互作用。我们用另一种细胞类型的条件培养基处理每种细胞类型。我们分析了对MC3T3-E1细胞细胞因子产生的影响以及对AM-3细胞基质金属蛋白酶产生的影响。用AM-3条件培养基处理可诱导MC3T3-E1细胞产生IL-6、MCP-1和RANTES等炎性细胞因子。使用IL-1受体拮抗剂可抑制用AM-3条件培养基刺激的MC3T3-E1细胞产生这些炎性细胞因子。MC3T3-E1条件培养基可触发AM-3细胞中MMP-2的表达。此外,我们还表明,MC-3T3-E1条件培养基可加速AM-3细胞的增殖和迁移活性。总之,成釉细胞瘤细胞与成骨细胞之间的这些细胞间信号传导可能在成釉细胞瘤的发病机制中发挥多种作用。