Curcumin protects human adipose-derived mesenchymal stem cells against oxidative stress-induced inhibition of osteogenesis

• Published in: Journal of pharmacological sciences Vol. 132; no. 3; pp. 192 - 200
• Main Authors: Wang, Nan, Wang, Feng, Gao, Youshui, Yin, Peipei, Pan, Chenhao, Liu, Wei, Zhou, Zubin, Wang, Jiaxiang
• Format: Journal Article
• Language: English
• Published: Japan Elsevier B.V 01.11.2016; Elsevier
• Subjects: Adipose Tissue - cytology; Adipose Tissue - drug effects; Adipose Tissue - metabolism; Cell Differentiation - drug effects; Cells, Cultured; Curcumin; Curcumin - pharmacology; Humans; Hydrogen Peroxide - pharmacology; Mesenchymal stem cell; Mesenchymal Stromal Cells - drug effects; Mesenchymal Stromal Cells - metabolism; Osteoblast differentiation; Osteoblasts - cytology; Osteoblasts - drug effects; Osteoblasts - metabolism; Osteogenesis - drug effects; Osteogenesis - physiology; Oxidative stress; Oxidative Stress - drug effects; Oxidative Stress - physiology; Wnt; Mesenchymal stem cell; Oxidative stress; Curcumin; Wnt; Osteoblast differentiation
• ISSN: 1347-8613; 1347-8648
• DOI: 10.1016/j.jphs.2016.10.005

The detrimental effects of oxidative stress on the skeletal system have been documented, and understanding the mechanisms is important to design a therapeutic strategy. As an antioxidant and anti-inflammatory agent, the active ingredient of turmeric curcumin has been used as medication for numerous complications including bone loss. However, it is unclear if curcumin could influence the osteogenic potential of mesenchymal stem cells (MSCs), particularly in oxidative injuries. Here we demonstrate that curcumin treatment protects cell death caused by hydrogen peroxide (H2O2) exposure in human adipose-derived MSCs in vitro. Importantly, curcumin is able to enhance the osteoblast differentiation of human adipose-derived MSCs that is inhibited by H2O2. Notably, both oxidative stress and the inhibition of Wnt/β-catenin signaling are attenuated by curcumin treatment. These results suggest that curcumin can promote osteoblast differentiation of MSCs and protect the inhibitory effect elicited by oxidative injury. The findings support potential use of curcumin or related antioxidants in MSC-based bone regeneration for disease related with oxidative stress-induced bone loss.