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Vaspin protects mouse mesenchymal stem cells from oxidative stress-induced apoptosis through the MAPK/p38 pathway

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Abstract

The aim of the work was to study the influence of vaspin on oxidative stress-induced apoptosis of mouse mesenchymal stem cells (MSCs). MSCs originated from bone marrow of C57BL/6 mouse were treated with vaspin and/or H2O2 in a dose-dependent manner. Cellular viability detected by CCK-8 and cell apoptosis studied by flow cytometry and TUNEL assay were observed in these cells. The protein expressions of PI3K, p-PI3K, Akt, p-Akt, T-ERK1/2, p-ERK1/2, p38, p-p38, JNK, and p-JNK were tested by Western blot. Vaspin had no significant effect on cellular viability, but significantly reduced H2O2-induced apoptosis. Western blot assay showed that pretreatment with vaspin promoted the activation of p-p38. Inhibition of p38 by SB203580 suppressed the protective effect of vaspin on oxidative stress-induced apoptosis. Vaspin inhibits oxidative stress-induced apoptosis of MSCs via the activation of MAPK/p38 signaling pathway. These findings indicate that vaspin is prone to osteoporosis protection.

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Funding

This study was funded by the National Natural Science Foundation of China (Grant No. 81400849); the Natural Science Foundation of Guangdong Province (Grant No. 2014A030310490); the Science and Technology Planning Project of Guangdong Province, China (Grant No. 2017A020215189); the Science and Technology Planning Project of Tianhe District, Guangdong Province, China (Grant No. 2013kw004).

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Correspondence to Jie Shen.

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Zhu, X., Zhang, L., Chen, Y. et al. Vaspin protects mouse mesenchymal stem cells from oxidative stress-induced apoptosis through the MAPK/p38 pathway. Mol Cell Biochem 462, 107–114 (2019). https://doi.org/10.1007/s11010-019-03614-8

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