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香菇水提乙酸乙酯部位通过抑制 NFATc1 表达抑制破骨细胞分化。

Ethyl Acetate Fraction of Aqueous Extract of Lentinula edodes Inhibits Osteoclastogenesis by Suppressing NFATc1 Expression.

机构信息

School of Biological Sciences, College of Natural Sciences, Chungbuk National University, Cheongju, Chungbuk 361-763, Korea.

Department of Industrial Plant Science and Technology, Chungbuk National University, Cheongju 28644, Korea.

出版信息

Int J Mol Sci. 2020 Feb 17;21(4):1347. doi: 10.3390/ijms21041347.

DOI:10.3390/ijms21041347
PMID:32079267
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7072883/
Abstract

Bone tissue is continuously remodeled by the coordinated action of osteoclasts and osteoblasts. Nuclear factor-activated T cells c1 (NFATc1) is a well-known transcription factor for osteoclastogenesis and transcriptionally activated by the c-Fos and nuclear factor-kappa B (NF-κB) signaling pathways in response to receptor activation of NF-κB ligand (RANKL). Since excessive RANKL signaling causes an increase of osteoclast formation and bone resorption, inhibition of RANKL or its signaling pathway is an attractive therapeutic approach to the treatment of pathologic bone loss. In this study, we show that an ethyl acetate fraction (LEA) from the shiitake mushroom, Lentinula edodes, inhibited RANKL-induced osteoclast differentiation by blocking the NFATc1 signaling pathway. We found that the water extract and its subsequent ethyl acetate fraction of L. edodes significantly suppressed osteoclast formation. Comparative transcriptome analysis revealed that LEA specifically downregulated a set of RANKL target genes, including Nfatc1. Next, we found that LEA suppresses Nfatc1 expression mainly through the inhibition of the transactivity of p65 and NFATc1. Moreover, treatment of LEA rescued an osteoporotic phenotype in a zebrafish model of glucocorticoid-induced osteoporosis. Collectively, our findings define an undocumented role of the shiitake mushroom extract in regulating bone development.

摘要

骨组织通过破骨细胞和成骨细胞的协调作用不断重塑。核因子激活 T 细胞 c1(NFATc1)是破骨细胞生成的一个众所周知的转录因子,它通过 c-Fos 和核因子-κB(NF-κB)信号通路转录激活,以响应 NF-κB 配体(RANKL)的受体激活。由于过量的 RANKL 信号导致破骨细胞形成和骨吸收增加,因此抑制 RANKL 或其信号通路是治疗病理性骨质流失的一种有吸引力的治疗方法。在这项研究中,我们表明,香菇(Lentinula edodes)的乙酸乙酯部分(LEA)通过阻断 NFATc1 信号通路抑制 RANKL 诱导的破骨细胞分化。我们发现,香菇的水提取物及其随后的乙酸乙酯部分显著抑制破骨细胞形成。比较转录组分析显示,LEA 特异性地下调了一组 RANKL 靶基因,包括 Nfatc1。接下来,我们发现 LEA 主要通过抑制 p65 和 NFATc1 的转活性来抑制 Nfatc1 的表达。此外,LEA 的治疗挽救了糖皮质激素诱导骨质疏松症斑马鱼模型中的骨质疏松表型。总之,我们的研究结果定义了香菇提取物在调节骨骼发育方面的一个未被记录的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfc4/7072883/29cb5dc3aa1f/ijms-21-01347-g005.jpg
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