Suppr超能文献

刺五加皂苷VI促进大鼠脂肪来源干细胞的成骨分化。

Asperosaponin VI stimulates osteogenic differentiation of rat adipose-derived stem cells.

作者信息

Ding Xingpo, Li Wuyin, Chen Dengshan, Zhang Chuanwei, Wang Lei, Zhang Hong, Qin Na, Sun Yongqiang

机构信息

Department of Pediatric Orthopaedics, Henan Luoyang Orthopedic Hospital (Henan Provincial Orthopedic Hospital), China.

Joint Department, Henan Luoyang Orthopedic Hospital (Henan Provincial Orthopedic Hospital), China.

出版信息

Regen Ther. 2019 May 10;11:17-24. doi: 10.1016/j.reth.2019.03.007. eCollection 2019 Dec.

Abstract

In the aging population, the decrease on osteogenic differentiation resulted into a significant reduction in bone formation. Bone tissue engineering has been a successful technique for treatment of bone defects. It is reported that adipose-derived stem cells (ADSCs) have pluripotency to differentiate into adipocytes and osteoblasts. However little is revealed about the effect of the herbal medicine Asperosaponin VI (ASA VI) on ADSCs differentiation. In our study, we isolated and identified ADSCs from rats. We examined the effect of different concentrations of ASA VI in ADSCs on alkaline phosphatase (ALP) activity, calcium deposition, the expression of bone-related proteins and the release of inflammatory cytokines. Flowcytometry assay showed ADSCs were highly expressed CD44 and CD105, but hardly expressed CD34 and CD45, suggesting ADSCs were successfully isolated for follow-up experiments. ALP activity examination and Alizarin red (AR) stain showed that ASA VI enhanced the ALP activity and promoted matrix mineralization in ADSCs. In addition, bone-related protein OCN and RUNX2, and Smad2/3 phosphorylation was upregulated after ASA VI treatment in ADSCs. ELISA results showed that ASA VI blocked the release of TNF-α, IL-6 and IL-1β in ADSCs. Considering this results, we concluded that ASA VI promotes osteogenic differentiation of ADSCs through inducing the expression of bone-related proteins. These findings enriched the function of ASA VI as a regenerative medicine and shed new light for the treatment of bone defects in clinical research.

摘要

在老龄化人群中,成骨分化能力的下降导致骨形成显著减少。骨组织工程已成为治疗骨缺损的一项成功技术。据报道,脂肪来源干细胞(ADSCs)具有分化为脂肪细胞和成骨细胞的多能性。然而,关于草药齐墩果酸皂苷VI(ASA VI)对ADSCs分化的影响却鲜有报道。在我们的研究中,我们从大鼠中分离并鉴定了ADSCs。我们检测了不同浓度的ASA VI对ADSCs中碱性磷酸酶(ALP)活性、钙沉积、骨相关蛋白表达以及炎性细胞因子释放的影响。流式细胞术检测显示ADSCs高表达CD44和CD105,但几乎不表达CD34和CD45,这表明ADSCs已成功分离,可用于后续实验。ALP活性检测和茜素红(AR)染色显示,ASA VI增强了ADSCs中的ALP活性并促进了基质矿化。此外,在ADSCs中用ASA VI处理后,骨相关蛋白骨钙素(OCN)和RUNX2以及Smad2/3磷酸化水平上调。酶联免疫吸附测定(ELISA)结果显示,ASA VI可抑制ADSCs中肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)和白细胞介素-1β(IL-1β)的释放。基于这些结果,我们得出结论,ASA VI通过诱导骨相关蛋白的表达促进ADSCs的成骨分化。这些发现丰富了ASA VI作为再生医学的功能,并为临床研究中骨缺损的治疗提供了新的思路。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验