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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
被引:0
|作者:
Bin Tang
Min Song
Xun Xie
Dongsheng Le
Qiulin Tu
Xiang Wu
Min Chen
机构:
[1] The First Affiliated Hospital of Nanchang University,Department of Neurosurgery
[2] The Second Clinical Medical College of Nanchang University,Department of Neurosurgery
[3] The Second Affiliated Hospital of Nanchang University,undefined
来源:
Neurochemical Research
|
2021年
/
46卷
关键词:
Intracerebral hemorrhage;
Blood brain barrier;
Bone mesenchymal stem cells;
TSG-6;
NF-κB signaling pathway;
D O I:
暂无
中图分类号:
学科分类号:
摘要:
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.
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页码:2387 / 2402
页数:15
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