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淫羊藿苷通过激活自噬促进骨髓基质细胞的成骨分化并预防去卵巢小鼠的骨丢失。

Icariin promotes osteogenic differentiation of bone marrow stromal cells and prevents bone loss in OVX mice via activating autophagy.

机构信息

Department of Orthopaedic Surgery, Zhongnan Hospital of Wuhan University, Wuhan, China.

The Institute for Brain Research, Collaborative Innovation Center for Brain Science, Huazhong University of Science and Technology, Wuhan, China.

出版信息

J Cell Biochem. 2019 Aug;120(8):13121-13132. doi: 10.1002/jcb.28585. Epub 2019 Mar 19.

Abstract

Osteoporosis (OP) results from the impaired function of endogenous bone marrow mesenchymal stem cells (BMSCs). Icariin (ICA) has shown potential osteoprotective effects. However, the molecular mechanism for the anabolic action of ICA remains largely unknown. The objective of the present study is to investigate whether ICA prevents bone loss by acting on BMSCs via affecting the level of autophagy after ovariectomy (OVX). The BMSCs were extracted from BALB/c mice treated with ICA, chloroquine (CQ, an autophagy inhibitor) or ICA + CQ. The OVX mice were injected with ICA, CQ, or ICA + CQ for 1 month. We performed Alizarin Red staining and alkaline phosphatase staining to detect osteogenic differentiation of BMSCs. Micro-CT, hematoxylin and eosin staining, Oil Red O staining, and tartrate-resistant acid phosphatase staining were used to assess the bone mass, lipid droplets and osteoclasts in femurs. Autophagy activity in BMSCs from different groups was evaluated by Western blot analysis. The osteogenic differentiation of BMSCs from OVX-induced OP mice was decreased. Treatment with ICA reduced bone loss and formation of osteoclasts and increased osteogenic differentiation of BMSCs in vitro and vivo. In addition, autophagy was enhanced in BMSCs of OVX mice treated with ICA. Our results indicate that ICA prevents OVX-induced bone loss possibly by strengthening the osteogenic differentiation of BMSCs via increasing autophagic activity.

摘要

骨质疏松症(OP)是由于内源性骨髓间充质干细胞(BMSCs)功能受损引起的。淫羊藿苷(ICA)已显示出潜在的护骨作用。然而,ICA 的合成作用的分子机制在很大程度上尚不清楚。本研究旨在探讨 ICA 是否通过影响去卵巢(OVX)后 BMSCs 自噬水平来防止骨丢失。从用 ICA、氯喹(CQ,自噬抑制剂)或 ICA+CQ 处理的 BALB/c 小鼠中提取 BMSCs。OVX 小鼠注射 ICA、CQ 或 ICA+CQ 1 个月。我们进行茜素红染色和碱性磷酸酶染色以检测 BMSCs 的成骨分化。微 CT、苏木精和伊红染色、油红 O 染色和抗酒石酸酸性磷酸酶染色用于评估股骨的骨量、脂肪滴和破骨细胞。通过 Western blot 分析评估不同组 BMSCs 的自噬活性。OVX 诱导的 OP 小鼠的 BMSCs 成骨分化减少。ICA 处理减少了骨丢失和破骨细胞的形成,并增强了体外和体内 OVX 小鼠的 BMSCs 成骨分化。此外,ICA 处理的 OVX 小鼠的 BMSCs 中自噬增强。我们的结果表明,ICA 可能通过增强自噬活性来增强 BMSCs 的成骨分化,从而防止 OVX 诱导的骨丢失。

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