Exosomes of Antler Mesenchymal Stem Cells Improve Postoperative Cognitive Dysfunction in Cardiopulmonary Bypass Rats through Inhibiting the TLR2/TLR4 Signaling Pathway.
Chun YangShengnan SunQi ZhangJia GuoTengfei WuYing LiuMin YangYan ZhangYinghua PengPublished in: Stem cells international (2020)
Postoperative cognitive dysfunction (POCD) is a severe complication of cardiopulmonary bypass (CPB) and has common characteristics such as acute cognitive dysfunction, impaired memory, and inattention. Mesenchymal stem cells (MSCs) are multipotent cells that have therapeutic potentials mainly through paracrine action via secreting growth factors and cytokines. Exosomes are one of the important paracrine factors and have been reported as potential cell-free therapy for the treatment of autoimmune and central nervous system disorders. In this study, we examined exosomes derived from antler MSCs (AMSCs) of POCD rats after CPB and evaluated their potential regulatory mechanisms. AMSC-derived exosomes reduced neurological damage and brain damage and prevent apoptosis in CPB rats. Furthermore, AMSC-derived exosomes were found to reduce hippocampal neuronal apoptosis and the expression of TLR2, TLR4, MyD88, and NF-κB in CPB rats. However, the above effects of AMSC-derived exosomes on CPB rats were abolished partially by toll-like receptor 2/4 (TLR2/TLR4) agonist (LPS-EB). In conclusion, AMSC-derived exosomes can improve cognitive function in CPB rats through inhibiting the TLR2/TLR4 signaling pathway.
Keyphrases
- toll like receptor
- mesenchymal stem cells
- inflammatory response
- signaling pathway
- nuclear factor
- umbilical cord
- immune response
- oxidative stress
- induced apoptosis
- stem cells
- bone marrow
- pi k akt
- cell cycle arrest
- lps induced
- cell free
- cell therapy
- patients undergoing
- epithelial mesenchymal transition
- endoplasmic reticulum stress
- intensive care unit
- drug induced
- multiple sclerosis
- early onset
- cerebral ischemia
- subarachnoid hemorrhage
- extracorporeal membrane oxygenation
- binding protein
- white matter
- cerebrospinal fluid
- risk assessment