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Mesenchymal stem cells promote proliferation of endogenous neural stem cells and survival of newborn cells in a rat stroke model

机译:间充质干细胞在大鼠中风模型中促进内源性神经干细胞的增殖和新生细胞的存活

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摘要

Mesenchymal stem cells (MSCs) secrete bioactive factors that exert diverse responses in vivo. In the present study, we explored mechanism how MSCs may lead to higher functional recovery in the animal stroke model. Bone marrow-derived MSCs were transplanted into the brain parenchyma 3 days after induction of stroke by occluding middle cerebral artery for 2 h. Stoke induced proliferation of resident neural stem cells in subventricular zone. However, most of new born cells underwent cell death and had a limited impact on functional recovery after stroke. Transplantation of MSCs enhanced proliferation of endogenous neural stem cells while suppressing the cell death of newly generated cells. Thereby, newborn cells migrated toward ischemic territory and differentiated in ischemic boundaries into doublecortin+ neuroblasts at higher rates in animals with MSCs compared to control group. The present study indicates that therapeutic effects of MSCs are at least partly ascribed to dual functions of MSCs by enhancing endogenous neurogenesis and protecting newborn cells from deleterious environment. The results reinforce the prospects of clinical application using MSCs in the treatment of neurological disorders.
机译:间充质干细胞(MSCs)分泌的生物活性因子可在体内发挥多种作用。在本研究中,我们探讨了在动物卒中模型中MSC可能导致更高功能恢复的机制。在中风诱发后3天,通过阻塞大脑中动脉2 h,将骨髓源性MSC移植到脑实质中。斯托克诱导心室下区驻留神经干细胞增殖。但是,大多数新生细胞会发生细胞死亡,并且对中风后的功能恢复影响有限。 MSC的移植增强了内源性神经干细胞的增殖,同时抑制了新生细胞的细胞死亡。因此,与对照组相比,具有MSCs的动物中新生细胞向缺血区域迁移,并在缺血边界分化为doublecortin + 成神经细胞。本研究表明,通过增强内源性神经发生并保护新生细胞免受有害环境的侵害,MSC的治疗作用至少部分归因于MSC的双重功能。该结果增强了使用MSC治疗神经系统疾病的临床应用前景。

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