Effect of Steroidal Hormone Pregnenolone on Proliferation and Differentiation of MC3T3-E1 Osteoblast like Cells

被引:2
作者
Badran, Serene Adnan [1 ]
Atia-tul-Wahab [2 ]
Fayyaz, Sharmeen [3 ]
Muhammad, Bushra Taj [2 ]
Choudhary, Muhammad Iqbal [2 ,3 ,4 ]
机构
[1] Univ Jordan, Fac Dent, Dept Pediat Dent & Orthodont, Amman 11942, Jordan
[2] Univ Karachi, Dr Panjwani Ctr Mol Med & Drug Res, Int Ctr Chem & Biol Sci, Karachi 75270, Pakistan
[3] Univ Karachi, Int Ctr Chem & Biol Sci, HEJ Res Inst Chem, Karachi 75270, Pakistan
[4] Univ Airlangga, Fac Sci & Technol, Dept Chem, Komplek Campus C, Surabaya 60115, Indonesia
关键词
Bone fragility diseases; osteoblast cells; osteoclast cells; MC3T3-E1; pregnenolone; alkaline phosphatase; ANDROGEN-DEPRIVATION THERAPY; OSTEOGENIC DIFFERENTIATION; RECEPTOR ACTIVATOR; OSTEOPOROSIS; PROMOTES;
D O I
10.2174/1570180817666200204110859
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Bone remodeling is a complex process that includes continuous resorption by osteoclast cells and bone formation by osteoblast cells. Bone fragility is a common health issue of the elderly population, particularly in postmenopausal women. It has been established that steroidal hormones have an important role in bone homeostasis. Therefore hormone replacement therapy could have beneficial effects on bone health as compared to other treatments. Objectives: An imbalance between the rate of bone formation and bone resorption leads to the fragility of bones. During the current study, we aimed to explore the ability of pregnenolone (1) (PRE), on proliferation and differentiation of MC3T3-E1 cells. We further aimed to investigate the underlying mechanism of action for the anabolic effect of PRE (1). Methods: The effects of pregnenolone (1) on proliferation, differentiation, and mineralization of MC3T3 osteoblast-like cells were determined. Cell viability was analyzed using MU assay and flow cytometry. ALP activity and alizarin staining were employed to evaluate the effect of pregnenolone on osteoblast differentiation. Moreover, western blot for analysis of certain important proteins, crucial for the regulation of bone homeostasis, such as BMP2 and RANKL, was also performed. Results and Discussions: Our results showed that pregnenolone (1) at a concentration of 5 mu M caused a significant (p< 0.05) rise in the growth of MC3T3-E1 cells, whereas a comparable effect was observed in osteoblast differentiating assays. A significant decrease in RANKL expression was observed at (0.04 -1 mu M). Our results, therefore, indicated the possible role of pregnenolone (1) in positive regulation of bone homeostasis by suppressing RANKL expression. Conclusion: Taken together, our results indicate that pregnenolone (1) has the potential to enhance osteoblast proliferation, as inferred from the increased number of cells. These results demonstrated that pregnenolone (1) could be a potential anabolic agent for the treatment of fragility related disorders.
引用
收藏
页码:1139 / 1145
页数:7
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