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补肾健脾活血方对成骨细胞中Beclin-1/Bcl-2介导的自噬和凋亡的影响

Efficacy of the Bushen Jianpi Huoxue Formula on Beclin-1/Bcl-2-mediated autophagy and apoptosis in osteoblasts.

作者信息

Lin Yanping, Zhao Rui, Huang Jiachun, Chen Tongying, Yang Haolin, Guo Haiwei, Wan Lei, Zhang Zhihai, Li Ying, Zhu Genfu, Huang Hongxing

机构信息

Department of Orthopedics, The Third Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, China.

The Third Clinical Medical School, Guangzhou University of Chinese Medicine, Guangzhou, China.

出版信息

Front Pharmacol. 2025 Jan 6;15:1513298. doi: 10.3389/fphar.2024.1513298. eCollection 2024.

Abstract

BACKGROUND

The Beclin-1/Bcl-2 complex plays a pivotal role in regulating both autophagy and apoptosis in osteoblasts affected by osteoporosis. This study first investigates whether the Bushen Jianpi Huoxue Formula can enhance the cellular function of osteoblasts. Additionally, it initially explores the functional mechanism of Beclin-1/Bcl-2-related apoptosis.

METHODS

Osteoblasts were isolated from the calvaria of three-day-old Sprague-Dawley female rats. The lyophilized power of the Bushen Jianpi Huoxue Formula was prepared from the following ingredients: Fructus Psoraleae, Epimedii Folium, Desertliving Cistanche, Prepared Rehmannia Radix, Radix paeoniae alba, Astragali Radix, Semen Cuscuta, Radix Salviae miltiorrhizae, Angelica sinensis, and Jujube. The primary components were detected by HPLC-MS. Beclin-1 overexpressed osteoblasts were constructed by transfection. Gene expression and protein level were examined by qRT-PCR and immunoblotting assay. Cell viability, apoptosis, and autophagy were assayed with CCK-8, flow cytometer, MDC staining, and Lyso-Tracker staining, respectively. Osteogenic differentiation was assayed by ALP staining, and mineralization by ARS staining. The complex of Beclin-1/Bcl-2 was detected by immunoprecipitation.

RESULTS

The results of this study indicated that the Bushen Jianpi Huoxue Formula could enhance both the proliferative activity, differentiation and mineralization of osteoblasts induced by Beclin-1 overexpression. This may be related to its role in activation of the WNT/β-CATENIN by increasing protein expression of WNT1 and β-CATENIN more than 1-fold. The formula effectively inhibited autophagy rate and apoptosis rate of osteoblasts by 50%. Furthermore, the formula was effective in attenuating endoplasmic reticulum stress by decreasing protein expression of AFT4, CHOP, eIF2α, and GRP78 more than 50%, which may play functions by suppressing the PERK signaling pathway. However, Mif treatment significantly weakened the effects of the formula.

CONCLUSION

Bushen Jianpi Huoxue Formula effectively enhanced the osteogenic activity by inhibiting Beclin-1-induced autophagy instead of the binding of Beclin-1 and Bcl-2. This underscores the formula's multifaceted role in promoting bone health and managing cellular stress, and offers novel insights into its therapeutic potential against osteoporosis.

摘要

背景

Beclin-1/Bcl-2复合物在调节受骨质疏松影响的成骨细胞的自噬和凋亡中起关键作用。本研究首先调查补肾健脾活血方是否能增强成骨细胞的细胞功能。此外,初步探究Beclin-1/Bcl-2相关凋亡的功能机制。

方法

从3日龄Sprague-Dawley雌性大鼠的颅骨中分离成骨细胞。补肾健脾活血方的冻干粉由以下成分制备:补骨脂、淫羊藿叶、肉苁蓉、熟地黄、白芍、黄芪、菟丝子、丹参、当归和大枣。通过HPLC-MS检测主要成分。通过转染构建Beclin-1过表达的成骨细胞。通过qRT-PCR和免疫印迹分析检测基因表达和蛋白质水平。分别用CCK-8、流式细胞仪、MDC染色和溶酶体追踪染料染色检测细胞活力、凋亡和自噬。通过ALP染色检测成骨分化,通过ARS染色检测矿化。通过免疫沉淀检测Beclin-1/Bcl-2复合物。

结果

本研究结果表明,补肾健脾活血方可以增强由Beclin-1过表达诱导的成骨细胞的增殖活性、分化和矿化。这可能与其通过使WNT1和β-连环蛋白的蛋白质表达增加超过1倍来激活WNT/β-连环蛋白有关。该方剂有效抑制成骨细胞的自噬率和凋亡率达50%。此外,该方剂通过使AFT4、CHOP、eIF2α和GRP78的蛋白质表达降低超过50%,有效减轻内质网应激,这可能通过抑制PERK信号通路发挥作用。然而,米氟处理显著削弱了该方剂的作用。

结论

补肾健脾活血方通过抑制Beclin-1诱导的自噬而非Beclin-1与Bcl-2的结合有效增强成骨活性。这凸显了该方剂在促进骨骼健康和应对细胞应激方面的多方面作用,并为其抗骨质疏松的治疗潜力提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72d7/11743543/c87361444214/fphar-15-1513298-g001.jpg

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