首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Hypothermia-Modulating Matrix Elasticity of Injured Brain Promoted Neural Lineage Specification of Mesenchymal Stem Cells
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Hypothermia-Modulating Matrix Elasticity of Injured Brain Promoted Neural Lineage Specification of Mesenchymal Stem Cells

机译:受损脑的低温调节基质弹性促进了间充质干细胞的神经谱系规范

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Both chemical and physical microenvironments appear to be important for lineage specification of umbilical cord mesenchymal stem cells (UCMSCs). However, physical factors such as the elastic modulus in traumatic brain injury (TBI) are seldom studied. Intracranial hypertension and cerebral edema after TBI may change the brain's physical microenvironment, which inhibits neural lineage specification of transplanted UCMSCs. The purpose of this study is to investigate the potential regulatory effect of mild hypothermia on the elastic modulus of the injured brain. First, we found that more UCMSCs grown on gels mimicking the elastic modulus of the brain (0.5 kPa) differentiated into neural cells, which were verified with the formation of branched cells and the expression of neural markers. Then, UCMSCs were transplanted into TBI rats, and we observed that mild hypothermia resulted in the differentiation of more neurons and astrocytes from transplanted UCMSCs. To demonstrate that more neural specification of UCMSCs was due to the regulation of the elastic modulus, we monitored intracranial pressure and cerebral edema. The results showed that mild hypothermia significantly reduced intracranial pressure and brain water content, indicating modulation of the elastic modulus by mild hypothermia. An examination with atomic force microscopy (AFM) in a cell injury model in vitro further verified hypothermia-regulated elastic modulus. In this study, we found a novel role of mild hypothermia in modulating the elastic modulus of the injured brain, resulting in the promotion of neural lineage specification of UCMSCs, which suggested that the combination of mild hypothermia had more advantages in cell-based therapy after TBI. (C) 2018 IBRO. Published by Elsevier Ltd. All rights reserved.
机译:化学和物理微环境似乎对脐带间充质干细胞(UCMSCs)的谱系规范很重要。然而,诸如在创伤性脑损伤(TBI)的弹性模量物理因素很少研究。 TBI后颅内高血压和脑水肿可以改变大脑的物理微环境,这抑制了移植的UCMSCs的神经谱系规范。本研究的目的是探讨轻度体温过低对受伤大脑弹性模量的潜在调节作用。首先,我们发现更多地在凝胶上生长的UCMSC,其模仿脑(0.5kPa)的弹性模量分化为神经细胞,以形成分支细胞和神经标记的表达。然后,将UCMSCs移植到TBI大鼠中,我们观察到温和的体温动下导致更多神经元和来自移植的UCMSCs的星形胶质细胞的分化。为了证明UCMSC的更多神经规格是由于弹性模量的调节,我们监测颅内压和脑水肿。结果表明,温和的体温过低显着降低颅内压力和脑含水量,表明通过温和体温过低的弹性模量的调节。在体外进行细胞损伤模型中原子力显微镜(AFM)的检查进一步验证了低温调节的弹性模量。在这项研究中,我们发现轻度体温过低在调节受伤性脑的弹性模量方面的一种新颖作用,从而促进了UCMSCs的神经谱系规范,这表明轻度体温过低的组合在基于细胞的疗法中具有更多优势TBI。 (c)2018年IBRO。 elsevier有限公司出版。保留所有权利。

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