Xianling Gubao attenuates high glucose-induced bone metabolism disorder in MG63 osteoblast-like cells

被引:5
作者
Chen, Xinlong [1 ,2 ,3 ]
Li, Yan [2 ,4 ]
Zhang, Zhongwen [1 ,2 ]
Chen, Liping [5 ]
Liu, Yaqian [5 ]
Huang, Shuhong [6 ]
Zhang, Xiaoqian [1 ,2 ]
机构
[1] Shandong First Med Univ, Shandong Key Lab Rheumat Dis & Translat Med, Dept Endocrinol & Metabol, Affiliated Hosp 1, Jinan, Shandong, Peoples R China
[2] Shandong Prov Qianfoshan Hosp, Shandong Inst Nephrol, Jinan, Shandong, Peoples R China
[3] Hosp Chengdu Univ Tradit Chinese Med, Chengdu, Sichuan, Peoples R China
[4] Shandong First Med Univ, Shandong Med & Hlth Key Lab Clin Pharm, Dept Clin Pharm, Affiliated Hosp 1, Jinan, Peoples R China
[5] Weifang Med Univ, Shandong Prov Qianfoshan Hosp, Dept Endocrinol & Metabol, Weifang, Peoples R China
[6] Shandong First Med Univ, Inst Basic Med, Affiliated Hosp 1, Jinan, Shandong, Peoples R China
来源
PLOS ONE | 2022年 / 17卷 / 12期
基金
中国国家自然科学基金;
关键词
DIABETES-MELLITUS; DIFFERENTIATION; OSTEOPOROSIS; FRACTURE; PATHWAY; INSULIN; TISSUES; TYPE-1; RISK;
D O I
10.1371/journal.pone.0276328
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Diabetes mellitus (DM) patients are prone to osteoporosis, and high glucose (HG) can affect bone metabolism. In the present study, we investigated the protective effects of traditional Chinese herbal formulation Xianling Gubao (XLGB) on HG-treated MG63 osteoblast-like cells. MG63 cells were incubated with control (mannitol), HG (20 mM glucose) or HG + XLGB (20 mM glucose+200 mg/L XLGB) mediums. Cell proliferation, apoptosis, migration and invasion were examined using CCK8, colony-formation, flow cytometry, Hoechst/PI staining, wound-healing and transwell assays, respectively. ELISA, RT-PCR and western blot analysis were used to detect the levels of osteogenesis differentiation-associated markers such as ALP, OCN, OPN, RUNX2, OPG, and OPGL in MG63 cells. The levels of the PI3K/Akt signaling pathway related proteins, cell cycle-related proteins, and mitochondrial apoptosis-related proteins were detected using western blot analysis. In HG-treated MG63 cells, XLGB significantly attenuated the suppression on the proliferation, migration and invasion of MG63 cells caused by HG. HG downregulated the activation of the PI3K/Akt signaling pathway and the expressions of cell cycle-related proteins, while XLGB reversed the inhibition of HG on MG63 cells. Moreover, XLGB significantly reduced the promotion on the apoptosis of MG63 cells induced by HG, the expressions of mitochondrial apoptosis-related proteins were suppressed by XLGB treatment. In addition, the expressions of osteogenesis differentiation-associated proteins were also rescued by XLGB in HG-treated MG63 cells. Our data suggest that XLGB rescues the MG63 osteoblasts against the effect of HG. The potential therapeutic mechanism of XLGB partially attributes to inhibiting the osteoblast apoptosis and promoting the bone formation of osteoblasts.
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页数:15
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