4.5 Article

Hypoxic Preconditioning Enhances the Efficacy of Mesenchymal Stem Cells-Derived Conditioned Medium in Switching Microglia toward Anti-inflammatory Polarization in Ischemia/Reperfusion

Journal

CELLULAR AND MOLECULAR NEUROBIOLOGY
Volume 41, Issue 3, Pages 505-524

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10571-020-00868-5

Keywords

Mesenchymal stem cells; Conditioned medium; Ischemia-reperfusion injury; Microglia; Hypoxic preconditioning; Immune regulation

Funding

  1. National Natural Science Foundation of China [81771707]
  2. Fundamental Research Funds for the Central Universities of China [2042018kf0235]

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The conditioned medium from BMSCs can effectively regulate the activation and polarization of I/R-stimulated microglia, promoting anti-inflammatory polarization. Particularly, BMSCs-CM from hypoxia preconditioning culture conditions showed enhanced efficacy in alleviating cell injury and promoting anti-inflammatory microglia polarization.
Activation of pro-inflammatory microglia is an important mechanism of the cerebral ischemia-reperfusion (I/R)-induced neuronal injury and dysfunction. Mesenchymal stem cells (MSCs) together with their paracrine factors demonstrated curative potential in immune disorders and inflammatory diseases, as well as in ischemic diseases. However, it remains unclear whether conditioned medium from MSCs could effectively regulate the activation and polarization of microglia exposed to I/R stimulation. In this study, we investigated the effects of conditioned medium from bone marrow MSCs (BMSCs-CM) on I/R-stimulated microglia and the potential mechanism involved, as well as the way to obtain more effective BMSCs-CM. First, cell model of oxygen-glucose deprivation/reoxygenation (OGD/R) was established in microglia to mimic the I/R. BMSCs-CM from different culture conditions (normoxic: 21% O-2; hypoxic: 1% O-2; hypoxia preconditioning: preconditioning with 1% O-2 for 24 h) was used to treat the microglia. Our results showed that BMSCs-CM effectively promoted the survival and alleviated the injury of microglia. Moreover, in microglia exposed to OGD/R, BMSCs-CM inhibited significantly the expression of pro-inflammatory cytokines (TNF-alpha, IL-1 beta, and IL-6), CD86 and inducible nitric oxide synthase, whereas upregulated the levels of anti-inflammatory cytokine (IL-10), CD206 and Arginase-1. These results suggested that BMSCs-CM promoted the polarization of anti-inflammatory microglia. In particular, BMSCs-CM from cultures with hypoxia preconditioning was more effective in alleviating cell injury and promoting anti-inflammatory microglia polarization than BMSCs-CM from normoxic cultures and from hypoxic cultures. Furthermore, inhibition of exosomes secretion could largely mitigate these effects of BMSCs-CM. In conclusion, our results suggested that hypoxia preconditioning of BMSCs could enhance the efficacy of BMSCs-CM in alleviating OGD/R-induced injury and in promoting the anti-inflammatory polarization of microglia, and these beneficial effects of BMSCs-CM owed substantially to exosomes.

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