Guangdong Engineering and Technology Research Center for Quality and Efficacy Re-evaluation of Post-marketed TCM, Guangdong Key Laboratory of Plant Resources, School of Life Sciences, Sun Yat-sen University, Guangzhou, People's Republic of China.
State Key Laboratory of Research on Bioactivities and Clinical Applications of Medicinal Plants (CUHK), LDS YYC R & D Centre for Chinese Medicine and School of Life Sciences, The Chinese University of Hong Kong, Hong Kong, China.
Int J Biol Macromol. 2020 May 15;151:1154-1162. doi: 10.1016/j.ijbiomac.2019.10.159. Epub 2019 Nov 18.
N16 is an active protein existing in Pinctada martensi. Our previous studies have demonstrated that N16 inhibited osteoclast differentiation in vitro. To better understand how N16 regulates osteoclast differentiation, RAW264.7 cells, a murine monocytic cell line and murine bone marrow-derived macrophages (BMMs) were adopted. Treatment of RAW264.7 cells with RANKL activated osteoclastogenesis and N16 inhibited the formation of multinucleated osteoclasts and TRAP activity. The suppression occurred at the early stage of osteoclastogenesis. Moreover, we found that N16 inhibited PU.1 and MITF expressions, mirroring the inhibition of RANK expressions, indicating that N16 inhibited RANK expression by down-regulating the expressions of MITF and PU.1, thus preventing osteoclastogenesis.
N16 是一种存在于马氏珠母贝中的活性蛋白。我们之前的研究表明,N16 可抑制体外破骨细胞的分化。为了更好地了解 N16 如何调节破骨细胞分化,我们采用了 RAW264.7 细胞(一种鼠单核细胞系)和鼠骨髓来源的巨噬细胞(BMMs)。用 RANKL 处理 RAW264.7 细胞可激活破骨细胞生成,而 N16 则抑制多核破骨细胞的形成和 TRAP 活性。这种抑制作用发生在破骨细胞生成的早期阶段。此外,我们发现 N16 抑制了 PU.1 和 MITF 的表达,与 RANK 表达的抑制相吻合,表明 N16 通过下调 MITF 和 PU.1 的表达抑制了 RANK 的表达,从而阻止了破骨细胞的生成。