Tumor Necrosis Factor-stimulated Gene-6 (TSG-6) Secreted by BMSCs Regulates Activated Astrocytes by Inhibiting NF-κB Signaling Pathway to Ameliorate Blood Brain Barrier Damage After Intracerebral Hemorrhage

Neurochem Res. 2021 Sep;46(9):2387-2402. doi: 10.1007/s11064-021-03375-1. Epub 2021 Jun 19.

Abstract

To investigate the influence of tumor necrosis factor-stimulated gene-6 (TSG-6) secreted by bone mesenchymal stem cells (BMSCs) on blood brain barrier (BBB) after intracerebral hemorrhage (ICH) and its related mechanisms. BMSCs and astrocytes were isolated and induced by TNF-α and LPS respectively. The effect of TSG-6 secreted by BMSCs on the proliferation and apoptosis of astrocytes and inflammatory response were assessed by CCK8, flow cytometry, and ELISA respectively. Then we studied the effects of TSG-6 secreted by BMSCs through the paracrine mechanism on the integrity of BBB after ICH via NF-κB signaling pathway in vitro and in vivo. We successfully isolated BMSCs and astrocytes. After LPS treatment of astrocytes, IL-1β, IL-6, and TNF-α showed an upward trend. TSG-6 secreted by TNF-α-activated BMSCs could antagonize the inflammatory response in activated astrocytes. Through the co-culture of astrocytes and BMSCs and the ICH animal model, we found that TSG-6 regulates activated astrocytes by inhibiting the NF-κB signaling pathway and ameliorates BBB damage. Furthermore, we found that TNF-α-activated BMSCs secreted exosomes containing TSG-6 and played an anti-inflammatory effect. TSG-6 secreted by BMSCs regulates activated astrocytes by inhibiting the NF-κB signaling pathway, thereby ameliorating BBB damage.

Keywords: Blood brain barrier; Bone mesenchymal stem cells; Intracerebral hemorrhage; NF-κB signaling pathway; TSG-6.

MeSH terms

  • Animals
  • Apoptosis / physiology
  • Astrocytes / drug effects
  • Astrocytes / metabolism*
  • Blood-Brain Barrier / physiology*
  • Cell Adhesion Molecules / metabolism*
  • Cell Proliferation / physiology
  • Cerebral Hemorrhage / metabolism*
  • Cytokines / metabolism
  • Exosomes / metabolism
  • Lipopolysaccharides / pharmacology
  • Male
  • Mesenchymal Stem Cells / metabolism*
  • NF-kappa B / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction / physiology*

Substances

  • Cell Adhesion Molecules
  • Cytokines
  • Lipopolysaccharides
  • NF-kappa B
  • Tnfaip6 protein, rat