A New Strategy for the Regulation of Neuroinflammation: Exosomes Derived from Mesenchymal Stem Cells.
Ying GeJingjing WuLi ZhangNanqu HuangYong LuoPublished in: Cellular and molecular neurobiology (2024)
Neuroinflammation is an important pathogenesis of neurological diseases and causes a series of physiopathological changes, such as abnormal activation of glial cells, neuronal degeneration and death, and disruption of the blood‒brain barrier. Therefore, modulating inflammation may be an important therapeutic tool for treating neurological diseases. Mesenchymal stem cells (MSCs), as pluripotent stem cells, have great therapeutic potential for neurological diseases due to their regenerative ability, immunity, and ability to regulate inflammation. However, recent studies have shown that MSC-derived exosomes (MSC-Exos) play a major role in this process and play a key role in neuroprotection by regulating neuroglia. This review summarizes the recent progress made in regulating neuroinflammation by focusing on the mechanisms by which MSC-Exos are involved in the regulation of glial cells through signaling pathways such as the TLR, NF-κB, MAPK, STAT, and NLRP3 pathways to provide some references for subsequent research and therapy.
Keyphrases
- mesenchymal stem cells
- cerebral ischemia
- signaling pathway
- induced apoptosis
- umbilical cord
- oxidative stress
- lps induced
- cell cycle arrest
- pi k akt
- bone marrow
- cell therapy
- traumatic brain injury
- lipopolysaccharide induced
- subarachnoid hemorrhage
- stem cells
- inflammatory response
- brain injury
- blood brain barrier
- endoplasmic reticulum stress
- epithelial mesenchymal transition
- cell proliferation
- neuropathic pain
- cell death
- toll like receptor
- spinal cord