Department of Biology, Faculty of Sciences, Arak University, Arak, Iran.
Endocr Metab Immune Disord Drug Targets. 2020;20(8):1336-1346. doi: 10.2174/1871530320666200505114058.
Previously, it was found that the para-nonylphenol (p-NP) impairs the osteogenic differentiation of rat bone marrow mesenchymal stem cells (rBMSCs); thus the aim of the present study was to evaluate the mechanism of the impairment.
rBMSCs after 3rd passage cultured in osteogenic media in the presence of 0, 0.5 and 2.5 μM p-NP for 5, 10, 15 and 20 days. The study investigated the viability of the cells using MTT assays. The mineralization was studied using Alizarin red quantification analysis. Using a flame-photometer, the electrolytes (sodium and potassium) were measured, and the level of calcium as well as ALT, AST, ALP and LDH was determined by commercial kits. The level of total-antioxidant, MDA and the activity of SOD and CAT were estimated with the help of a spectrophotometer. Gene expression was studied using rt-PCR.
The p-NP treatment of osteogenic differentiated MSCs showed intracellular electrolyte imbalance and variation of cellular metabolism. In addition, we observed oxidative stress due to the reduction of total antioxidant capacity and the imbalance of antioxidant enzymes activity. Investigating the genes involved in the osteogenic differentiation of MSCs to osteoblast showed that the 2.5 μM of p-NP reduced the expression of the ALP, SMAD, BMP and RUNX2 genes.
The study concludes that this pollutant via influencing the genomics and metabolic imbalance, as well as oxidative induction, caused a reduction of mineralization and differentiation of MSCs. This environmental pollutant might cause osteoporosis, which necessitates raising public awareness, especially to those who live in the industrial area to prevent its drastic effect.
此前研究发现,对壬基酚(p-NP)会损害大鼠骨髓间充质干细胞(rBMSCs)的成骨分化;因此,本研究旨在评估其损伤机制。
第 3 代 rBMSC 在成骨培养基中培养,分别加入 0、0.5 和 2.5μM p-NP,作用 5、10、15 和 20 天。采用 MTT 法检测细胞活力。茜素红比色法检测矿化程度。采用火焰光度计检测电解质(钠和钾),采用商业试剂盒检测钙以及 ALT、AST、ALP 和 LDH 水平。通过分光光度计评估总抗氧化能力、MDA 水平以及 SOD 和 CAT 活性。采用 rt-PCR 检测基因表达。
p-NP 处理成骨分化的 MSC 表现出细胞内电解质失衡和细胞代谢变化。此外,我们观察到氧化应激,这是由于总抗氧化能力降低和抗氧化酶活性失衡引起的。对参与 MSC 向成骨细胞分化的基因进行研究发现,2.5μM 的 p-NP 降低了 ALP、SMAD、BMP 和 RUNX2 基因的表达。
本研究表明,这种污染物通过影响基因组和代谢失衡以及氧化诱导,导致 MSC 矿化和分化减少。这种环境污染物可能导致骨质疏松症,因此需要提高公众意识,特别是生活在工业区的人群,以预防其严重影响。