Department of Cancer Biology and Pharmacology, University of Illinois College of Medicine at Peoria, Peoria, IL, USA.
Department of Internal Medicine, Rush University Medical Center, Chicago, IL, USA.
Neuromolecular Med. 2019 Dec;21(4):529-539. doi: 10.1007/s12017-019-08540-y. Epub 2019 May 10.
Emerging stroke literature suggests that treatment of experimentally induced stroke with stem cells offered post-stroke neuroprotection via exosomes produced by these cells. Treatment with exosomes has great potential to overcome the limitations associated with cell-based therapies. However, in our preliminary studies, we noticed that the exosomes released from human umbilical cord blood-derived mesenchymal stem cells (MSCs) under standard culture conditions did not improve the post-stroke neurological outcome. Because of this apparent discrepancy, we hypothesized that exosome characteristics vary with the conditions of their production. Specifically, we suggest that the exosomes produced from the cocultures of regular and oxygen-glucose-deprived (OGD) MSCs in vitro would represent the exosomes produced from MSCs that are exposed to ischemic brain cells in vivo, and offer similar therapeutic benefits that the cell treatment would provide. We tested the efficacy of therapy with exosomes secreted from human umbilical cord blood (HUCB)-derived MSCs under in vitro hypoxic conditions on post-stroke brain damage and neurological outcome in a rat model of transient focal cerebral ischemia. We performed the TTC staining procedure as well as the neurological tests including the modified neurological severity scores (mNSS), the modified adhesive removal (sticky-tape), and the beam walking tests before ischemia and at regular intervals until 7 days reperfusion. Treatment with exosomes obtained from the cocultures of normal and OGD-induced MSCs reduced the infarct size and ipsilateral hemisphere swelling, preserved the neurological function, and facilitated the recovery of stroke-induced rats. Based on the results, we conclude that the treatment with exosomes secreted from MSCs at appropriate experimental conditions attenuates the post-stroke brain damage and improves the neurological outcome.
新兴的中风文献表明,通过这些细胞产生的外泌体,用干细胞治疗实验性中风可以提供中风后的神经保护。用外泌体治疗具有克服与细胞治疗相关的限制的巨大潜力。然而,在我们的初步研究中,我们注意到,在标准培养条件下,从人脐带血来源的间充质干细胞(MSCs)释放的外泌体并没有改善中风后的神经功能结果。由于这种明显的差异,我们假设外泌体的特征随其产生条件的变化而变化。具体来说,我们建议,在体外将常规和缺氧-葡萄糖剥夺(OGD)MSCs 共培养产生的外泌体,代表了暴露于体内缺血性脑细胞的 MSC 产生的外泌体,并提供与细胞治疗相似的治疗益处。我们在短暂性局灶性脑缺血大鼠模型中,检测了在体外缺氧条件下,人脐带血(HUCB)来源的 MSC 分泌的外泌体对中风后脑损伤和神经功能结果的治疗效果。我们进行了 TTC 染色程序以及神经学测试,包括改良神经严重程度评分(mNSS)、改良粘连去除(粘性胶带)和横梁行走测试,在缺血前和定期间隔直到 7 天再灌注。用正常和 OGD 诱导的 MSC 共培养物获得的外泌体治疗,可减少梗死面积和同侧半球肿胀,保留神经功能,并促进中风诱导大鼠的恢复。基于这些结果,我们得出结论,用适当的实验条件分泌的 MSC 分泌的外泌体治疗可以减轻中风后的脑损伤并改善神经功能结果。