Platelet-rich plasma-derived exosomes boost mesenchymal stem cells to promote peripheral nerve regeneration

被引:6
|
作者
Zhang, Yongyi [1 ,2 ,3 ,4 ,5 ]
Yi, Dan [1 ,6 ]
Hong, Quan [4 ]
Cao, Jiangbei [7 ]
Geng, Xiaodong [4 ]
Liu, Jinwei [1 ,2 ,3 ]
Xu, Chuang [1 ,2 ,3 ]
Cao, Mengyu [2 ,3 ]
Chen, Chao [1 ,2 ,3 ]
Xu, Shuaixuan [1 ,2 ,3 ]
Zhang, Zhen [1 ,2 ,3 ]
Li, Molin [1 ,6 ]
Zhu, Yaqiong [6 ]
Peng, Nan [1 ,2 ,3 ]
机构
[1] Med Sch Chinese PLA, Beijing 100853, Peoples R China
[2] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 2, Dept Rehabil Med, Beijing 100853, Peoples R China
[3] Chinese Peoples Liberat Army Gen Hosp, Natl Clin Res Ctr Geriatr Dis, Beijing 100853, Peoples R China
[4] Chinese Peoples Liberat Army Gen Hosp, Nephrol Inst Chinese PLA, Natl Clin Res Ctr Kidney Dis, Med Ctr 1,State Key Lab Kidney Dis,Beijing Key Lab, Beijing 100853, Peoples R China
[5] No 962 Hosp PLA Joint Logist Support Force, Harbin 150080, Peoples R China
[6] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Ultrasound, Beijing 100853, Peoples R China
[7] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Anaesthesiol, Beijing 100853, Peoples R China
关键词
Platelet -rich plasma -derived exosomes; Umbilical cord -derived mesenchymal stem cell; Peripheral nerve injury; Glia-derived neurotrophic factor; Cell therapy; Nerve regeneration; INJURY; REPAIR; ACTIVATION; PARACRINE; HYDROGELS; SURVIVAL; SHEETS; GDNF;
D O I
10.1016/j.jconrel.2024.01.043
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Peripheral nerve injury (PNI) remains a severe clinical problem with debilitating consequences. Mesenchymal stem cell (MSC)-based therapy is promising, but the problems of poor engraftment and insufficient neurotrophic effects need to be overcome. Herein, we isolated platelet-rich plasma-derived exosomes (PRP-Exos), which contain abundant bioactive molecules, and investigated their potential to increase the regenerative capacity of MSCs. We observed that PRP-Exos significantly increased MSC proliferation, viability, and mobility, decreased MSC apoptosis under stress, maintained MSC stemness, and attenuated MSC senescence. In vivo, PRP-Exo-treated MSCs (pExo-MSCs) exhibited an increased retention rate and heightened therapeutic efficacy, as indicated by increased axonal regeneration, remyelination, and recovery of neurological function in a PNI model. In vitro, pExo-MSCs coculture promoted Schwann cell proliferation and dorsal root ganglion axon growth. Moreover, the increased neurotrophic behaviour of pExo-MSCs was mediated by trophic factors, particularly glia-derived neurotrophic factor (GDNF), and PRP-Exos activated the PI3K/Akt signalling pathway in MSCs, leading to the observed phenotypes. These findings demonstrate that PRP-Exos may be novel agents for increasing the ability of MSCs to promote neural repair and regeneration in patients with PNI.
引用
收藏
页码:265 / 282
页数:18
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