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筋骨草乙酸乙酯和正丁醇部位促进小鼠前成骨细胞株 MC3T3-E1(亚克隆 4)的矿化潜能。

Ethyl acetate and n-butanol fraction of Cissus quadrangularis promotes the mineralization potential of murine pre-osteoblast cell line MC3T3-E1 (sub-clone 4).

机构信息

School of Biological Sciences, University of the Punjab, Quaid-i-Azam Campus, Lahore, Pakistan.

Department of Biotechnology, Kinnaird College for Women, Lahore, Pakistan.

出版信息

J Cell Physiol. 2019 Jul;234(7):10300-10314. doi: 10.1002/jcp.27707. Epub 2018 Nov 15.

Abstract

In a sequel to investigate osteogenic potential of ethanolic extract of Cissus quadrangularis (CQ), the present study reports the osteoblast differentiation and mineralization potential of ethyl acetate (CQ-EA) and butanol (CQ-B) extracts of CQ on mouse pre-osteoblast cell line MC3T3-E1 (sub-clone 4) with an objective to isolate an antiosteoporotic compound. Growth curve, proliferation, and viability assays showed that both the extracts were nontoxic to the cells even at high concentration (100 µg/ml). The cell proliferation was enhanced at low concentrations (0.1 µg/ml and 1 µg/ml) of both the extracts. They also upregulated the osteoblast differentiation and mineralization processes in MC3T3-E1 cells as reflected by expression profile of osteoblast marker genes such as RUNX2, Osterix, Collagen (COL1A1), Alkaline Phosphatase (ALP), Integrin-related Bone Sialoprotein (IBSP), Osteopontin (OPN), and Osteocalcin (OCN). CQ-EA treatment resulted in early differentiation and mineralization as compared with the CQ-B treatment. These findings suggest that low concentrations of CQ-EA and CQ-B have proliferative and osteogenic properties. CQ-EA, however, is more potent osteogenic than CQ-B.

摘要

为了分离一种抗骨质疏松化合物,本研究继研究印度菝葜的乙醇提取物(CQ)的成骨潜能后,报告了印度菝葜的乙酸乙酯(CQ-EA)和正丁醇(CQ-B)提取物对小鼠前成骨细胞系 MC3T3-E1(亚克隆 4)的成骨细胞分化和矿化潜能。生长曲线、增殖和活力测定表明,即使在高浓度(100μg/ml)下,两种提取物对细胞均无毒性。两种提取物的低浓度(0.1μg/ml 和 1μg/ml)均能增强细胞增殖。它们还上调了 MC3T3-E1 细胞中的成骨细胞分化和矿化过程,反映在成骨细胞标志物基因如 RUNX2、Osterix、胶原(COL1A1)、碱性磷酸酶(ALP)、整合素相关骨涎蛋白(IBSP)、骨桥蛋白(OPN)和骨钙素(OCN)的表达谱上。与 CQ-B 处理相比,CQ-EA 处理导致早期分化和矿化。这些发现表明,CQ-EA 和 CQ-B 的低浓度具有增殖和成骨特性。然而,CQ-EA 的成骨作用比 CQ-B 更强。

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