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6-羟基黄酮对 MC3T3-E1 细胞成骨细胞分化的影响。

Effects of 6-Hydroxyflavone on Osteoblast Differentiation in MC3T3-E1 Cells.

机构信息

Department of Physical Medicine and Rehabilitation, School of Medicine, College of Medicine, Taipei Medical University (TMU), No. 250, Wuxing Street, Taipei 11031, Taiwan ; Department of Physical Medicine and Rehabilitation, Taipei Medical University Hospital (TMUH), No. 252, Wuxing Street, Taipei 11031, Taiwan ; International Institute of Nano Biomedicine, TMU, No. 252, Wuxing Street, Taipei 11031, Taiwan.

Graduate Institute of Medical Sciences, College of Medicine, TMU, No. 250, Wuxing Street, Taipei 11031, Taiwan ; Center for Teeth Bank and Dental Stem Cell Technology, TMU, No. 250, Wuxing Street, Taipei 11031, Taiwan.

出版信息

Evid Based Complement Alternat Med. 2014;2014:924560. doi: 10.1155/2014/924560. Epub 2014 Mar 26.

Abstract

Osteoblast differentiation plays an essential role in bone integrity. Isoflavones and some flavonoids are reported to have osteogenic activity and potentially possess the ability to treat osteoporosis. However, limited information concerning the osteogenic characteristics of hydroxyflavones is available. This study investigates the effects of various hydroxyflavones on osteoblast differentiation in MC3T3-E1 cells. The results showed that 6-hydroxyflavone (6-OH-F) and 7-hydroxyflavone (7-OH-F) stimulated ALP activity. However, baicalein and luteolin inhibited ALP activity and flavone showed no effect. Up to 50  μ M of each compound was used for cytotoxic effects study; flavone, 6-OH-F, and 7-OH-F had no cytotoxicity on MC3T3-E1 cells. Moreover, 6-OH-F activated AKT and serine/threonine kinases (also known as protein kinase B or PKB), extracellular signal-regulated kinases (ERK 1/2), and the c-Jun N-terminal kinase (JNK) signaling pathways. On the other hand, 7-OH-F promoted osteoblast differentiation mainly by activating ERK 1/ 2 signaling pathways. Finally, after 5 weeks of 6-OH-F induction, MC3T3-E1 cells showed a significant increase in the calcein staining intensity relative to merely visible mineralization observed in cells cultured in the osteogenic medium only. These results suggested that 6-OH-F could activate AKT, ERK 1/2, and JNK signaling pathways to effectively promote osteoblastic differentiation.

摘要

成骨细胞分化在骨完整性中起着至关重要的作用。异黄酮和一些类黄酮被报道具有成骨活性,并有潜力治疗骨质疏松症。然而,关于羟基黄酮的成骨特性的信息有限。本研究调查了各种羟基黄酮对 MC3T3-E1 细胞成骨分化的影响。结果表明,6-羟基黄酮(6-OH-F)和 7-羟基黄酮(7-OH-F)刺激 ALP 活性。然而,黄芩素和木犀草素抑制 ALP 活性,而黄酮则没有作用。使用高达 50 μM 的每种化合物进行细胞毒性作用研究;黄酮、6-OH-F 和 7-OH-F 对 MC3T3-E1 细胞没有细胞毒性。此外,6-OH-F 激活 AKT 和丝氨酸/苏氨酸激酶(也称为蛋白激酶 B 或 PKB)、细胞外信号调节激酶(ERK 1/2)和 c-Jun N-末端激酶(JNK)信号通路。另一方面,7-OH-F 主要通过激活 ERK 1/2 信号通路促进成骨细胞分化。最后,经过 6-OH-F 诱导 5 周后,MC3T3-E1 细胞的钙黄绿素染色强度相对于仅在成骨培养基中培养的细胞观察到的仅可见矿化有明显增加。这些结果表明,6-OH-F 可以激活 AKT、ERK 1/2 和 JNK 信号通路,有效促进成骨细胞分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30f3/3984785/3bfe3be4c82d/ECAM2014-924560.001.jpg

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