Wang Yonghui, Xia Chao, Chen Yang, Jiang Tianyuan, Hu Yan, Gao Yanhong
Department of Geriatrics, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Department of Geriatrics, Shanghai General Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Stem Cells Int. 2022 Jul 25;2022:8124085. doi: 10.1155/2022/8124085. eCollection 2022.
Mesenchymal stem cells (MSCs) differentiate into osteocytes, adipocytes, and chondrocytes. Resveratrol and bone morphogenetic protein 9 (BMP9) are known osteogenic induction factors of MSCs, but the effect of both resveratrol and BMP9 on osteogenesis is unknown. Herein, we explored whether resveratrol cooperates with BMP9 to improve osteogenic induction.
The osteogenic induction of resveratrol and BMP9 on C3H10T1/2 cells was evaluated by detecting the staining and activity of the early osteogenic marker alkaline phosphatase (ALP). In addition, the late osteogenic effect was measured by the mRNA and protein levels of osteogenic markers, such as osteopontin (OPN) and osteocalcin (OCN). To assess the bone formation function of resveratrol plus BMP9 , we transplanted BMP9-infected C3H10T1/2 cells into nude mice followed by intragastric injection of resveratrol. Western blot (WB) analysis was utilized to elucidate the mechanism of resveratrol plus BMP9.
Resveratrol not only enhanced osteogenic induction alone but also improved BMP9-induced ALP at 3, 5, and 7 d postinduction. Both the early osteogenic markers (ALP, Runx2, and SP7) and the late osteogenic markers (OPN and OCN) were significantly increased when resveratrol was combined with BMP9. The fetal limb explant culture further verified these results. The bone formation experiment, which involved transplanting BMP9-overexpressing C3H10T1/2 cells into nude mice, also confirmed that resveratrol synergistically enhanced the BMP9-induced bone formation function. Resveratrol phosphorylated adenosine monophosphate- (AMP-) activated protein kinase (AMPK) and stimulated autophagy, but these effects were abolished by inhibiting AMPK and Beclin1 using an inhibitor or siRNA.
Resveratrol combined with BMP9 significantly improves the osteogenic induction of C3H10T1/2 cells by activating AMPK and autophagy.
间充质干细胞(MSCs)可分化为骨细胞、脂肪细胞和软骨细胞。白藜芦醇和骨形态发生蛋白9(BMP9)是已知的MSCs成骨诱导因子,但白藜芦醇和BMP9对成骨的影响尚不清楚。在此,我们探讨了白藜芦醇是否与BMP9协同作用以改善成骨诱导。
通过检测早期成骨标志物碱性磷酸酶(ALP)的染色和活性,评估白藜芦醇和BMP9对C3H10T1/2细胞的成骨诱导作用。此外,通过成骨标志物如骨桥蛋白(OPN)和骨钙素(OCN)的mRNA和蛋白水平来测定晚期成骨效应。为了评估白藜芦醇加BMP9的骨形成功能,我们将感染BMP9的C3H10T1/2细胞移植到裸鼠体内,随后灌胃给予白藜芦醇。利用蛋白质印迹法(WB)分析来阐明白藜芦醇加BMP9的作用机制。
白藜芦醇不仅单独增强成骨诱导作用,还在诱导后第3、5和7天改善了BMP9诱导的ALP。当白藜芦醇与BMP9联合使用时,早期成骨标志物(ALP、Runx2和SP7)和晚期成骨标志物(OPN和OCN)均显著增加。胎儿肢体外植体培养进一步证实了这些结果。将过表达BMP9的C3H10T1/2细胞移植到裸鼠体内的骨形成实验也证实,白藜芦醇协同增强了BMP9诱导的骨形成功能。白藜芦醇使腺苷单磷酸-(AMP-)激活蛋白激酶(AMPK)磷酸化并刺激自噬,但使用抑制剂或小干扰RNA(siRNA)抑制AMPK和Beclin1可消除这些作用。
白藜芦醇与BMP9联合使用可通过激活AMPK和自噬显著改善C3H10T1/2细胞的成骨诱导作用。