2022
DOI: 10.4103/1673-5374.314323
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Exosomes derived from bone marrow mesenchymal stem cells protect the injured spinal cord by inhibiting pericyte pyroptosis

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Cited by 68 publications
(7 citation statements)
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“…Therefore, the targeting of pyroptosis in other cell types may im- prove histological and functional outcomes after SCI. Zhou et al [115] reported that exosomes derived from bone marrow mesenchymal stem cells effectively reduced pericellular pyroptosis, improved the integrity of the blood-spinal barrier, and promoted functional recovery after SCI. It was also reported that astrocytes play a role in neuroinflammation.…”
Section: Other Cell Typesmentioning
confidence: 99%
“…Therefore, the targeting of pyroptosis in other cell types may im- prove histological and functional outcomes after SCI. Zhou et al [115] reported that exosomes derived from bone marrow mesenchymal stem cells effectively reduced pericellular pyroptosis, improved the integrity of the blood-spinal barrier, and promoted functional recovery after SCI. It was also reported that astrocytes play a role in neuroinflammation.…”
Section: Other Cell Typesmentioning
confidence: 99%
“…Extracellular vesicles (EVs) are extracellular lipid membrane-bound particles that contain host cell-derived protein or nucleic acid messengers, and have an effect on target cells via paracrine or autocrine regulatory functions [17]. This new type of therapy has the potential to change the microenvironment of healing tissue, reducing the inflammatory process and promoting regeneration, as shown in various studies across different organ systems, such as neural [18], musculoskeletal [19], and cardiac [20] tissues. This systematic review explores whether mesenchymal stem cell-derived extracellular vesicles (MSC-EVs) can facilitate tendon/ligament repair in vivo.…”
Section: Of 30mentioning
confidence: 99%
“…Regarding concomitant injuries there are currently no data, but further reduced cell survival due to compromised local perfusion and dysregulated systemic and local energy metabolism such as hyperglycaemia is very likely. Concerning secrotomic capacity, it has been shown that inflammatory cytokines inhibit the proangiogenic capacity of the soluble component of the MSC secretome [ 280 ], and that the secretomic capacity of BM-MSCs is crucial for the promotion of neuronal survival after TSCI [ 281 ].…”
Section: Tbi Tsci and Mscsmentioning
confidence: 99%