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脐带间充质干细胞来源的神经球促进实验性中风的长期功能恢复,但加重急性期炎症。

Umbilical Cord Mesenchymal Stem Cells Derived Neurospheres Promote Long-term functional recovery But Aggravate Acute Phase Inflammation in Experimental Stroke.

机构信息

Stem Cell Center, Department of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, PR China.

Department of Neurology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, PR China.

出版信息

Neuroscience. 2022 Jan 1;480:217-228. doi: 10.1016/j.neuroscience.2021.10.032. Epub 2021 Nov 9.

Abstract

Human umbilical cord mesenchymal stem cells (UC-MSCs) transplantation has been shown to ameliorate intracerebral hemorrhage (ICH) in animal and clinical studies. We previously reported an easy one-step method to induce UC-MSCs into neurospheres with much enhanced neurogenic and angiogenic potential. In the present study, we further evaluated the neuro-protective effects of these UC-MSCs derived neurospheres (UC-MSCs-NS) using a murine collagenase induced ICH model. We compared the effects of UC-MSCs or UC-MSCs-NS transplantation at two different time-points: 3 h after ICH induction (early transplantation) or three days after ICH induction (delayed transplantation). The results showed that UC-MSCs exhibited favorable effects at both time-points whereas UC-MSCs-NS early delivery led to increased cell apoptosis, exacerbated brain edema, enlarged ICH volume and deteriorated neurological function. In vivo inflammatory cytokine analysis indicated UC-MSCs transplantation was able to attenuate the acute phase secretion of inflammatory cytokines TNF-α and IL-1β whereas UC-MSCs-NS immediate transplantation led to increased levels of these cytokines. However, long-term follow-up experiment showed delayed UC-MSCs-NS transplantation was superior to UC-MSCs transplantation alone in terms of increased neurogenic reconstitution. Our results suggest both UC-MSCs and UC-MSCs-NS can exert favorable effects in ICH therapy but the infusion of UC-MSCs-NS should avoid the super-early phase of ICH. We believe UC-MSCs derived neurospheres should be further exploited for chronic refractory neurological disorders such as chronic phase of stroke and various neurodegenerative disorders such as Alzheimer's disease.

摘要

人脐带间充质干细胞(UC-MSCs)移植已被证明可改善动物和临床研究中的脑出血(ICH)。我们之前报道了一种简单的一步法,可将 UC-MSCs 诱导为具有更强神经发生和血管生成潜力的神经球。在本研究中,我们使用鼠胶原酶诱导的 ICH 模型进一步评估了这些 UC-MSCs 衍生的神经球(UC-MSCs-NS)的神经保护作用。我们比较了 UC-MSCs 或 UC-MSCs-NS 移植在两个不同时间点的效果:ICH 诱导后 3 小时(早期移植)或 ICH 诱导后三天(延迟移植)。结果表明,UC-MSCs 在两个时间点均表现出良好的效果,而 UC-MSCs-NS 早期给药导致细胞凋亡增加、脑水肿加重、ICH 体积增大和神经功能恶化。体内炎性细胞因子分析表明,UC-MSCs 移植能够减轻 TNF-α和 IL-1β等急性期炎性细胞因子的分泌,而 UC-MSCs-NS 即刻移植则导致这些细胞因子水平升高。然而,长期随访实验表明,延迟 UC-MSCs-NS 移植在增加神经发生重建方面优于单独 UC-MSCs 移植。我们的结果表明,UC-MSCs 和 UC-MSCs-NS 均可在 ICH 治疗中发挥有利作用,但 UC-MSCs-NS 的输注应避免 ICH 的超早期阶段。我们相信,UC-MSCs 衍生的神经球应该进一步用于慢性难治性神经疾病,如中风的慢性期和各种神经退行性疾病,如阿尔茨海默病。

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