首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Astroglial Activation by an Enriched Environment after Transplantation of Mesenchymal Stem Cells Enhances Angiogenesis after Hypoxic-Ischemic Brain Injury
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Astroglial Activation by an Enriched Environment after Transplantation of Mesenchymal Stem Cells Enhances Angiogenesis after Hypoxic-Ischemic Brain Injury

机译:骨髓间充质干细胞移植后富集环境对星形胶质细胞的激活增强了缺氧缺血性脑损伤后的血管生成。

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摘要

Transplantation of mesenchymal stem cells (MSCs) has paracrine effects; however, the effects are known to be largely limited. Here we investigated the combination effects of cell transplantation and enriched environment (EE) in a model of hypoxic-ischemic brain injury. Brain damage was induced in seven-day-old mice by unilateral carotid artery ligation and exposure to hypoxia (8% O2 for 90 min). At six weeks of age, the mice were randomly assigned to four groups: phosphate-buffered saline (PBS)-control (CON), PBS-EE, MSC-CON, and MSC-EE. Rotarod and grip strength tests were performed to evaluate neurobehavioral functions. Histologic evaluations were also performed to confirm the extent of astrocyte activation and endogenous angiogenesis. An array-based multiplex ELISA and Western blot were used to identify growth factors in vivo and in vitro. Two weeks after treatment, levels of astrocyte density and angiogenic factors were increased in MSC-EE mice, but glial scarring was not increased. Eight weeks after treatment, angiogenesis was increased, and behavioral outcomes were synergistically improved in the MSC-EE group. Astrocytes co-cultured with MSCs expressed higher levels of angiogenic factors than astrocytes cultured alone. The mechanisms of this synergistic effect included enhanced repair processes, such as increased endogenous angiogenesis and upregulation of angiogenic factors released from activated astrocytes.
机译:间充质干细胞(MSCs)的移植具有旁分泌作用。但是,已知效果受到很大限制。在这里,我们研究了缺氧缺血性脑损伤模型中细胞移植和丰富环境(EE)的联合作用。通过单侧颈动脉结扎和暴露于缺氧(8%的氧气,持续90分钟),在7日龄的小鼠中诱发了脑损伤。在六周大时,将小鼠随机分为四组:磷酸盐缓冲液(PBS)-对照(CON),PBS-EE,MSC-CON和MSC-EE。进行了Rotarod和握力测试以评估神经行为功能。还进行了组织学评估,以确认星形胶质细胞激活和内源性血管生成的程度。基于阵列的多重ELISA和Western印迹用于鉴定体内和体外生长因子。治疗后两周,MSC-EE小鼠的星形胶质细胞密度和血管生成因子水平增加,但神经胶质瘢痕形成并未增加。治疗八周后,MSC-EE组的血管生成增加,行为结果协同改善。与MSC共培养的星形胶质细胞比单独培养的星形胶质细胞表达更高水平的血管生成因子。这种协同作用的机制包括增强的修复过程,例如增加内源性血管生成和激活星形胶质细胞释放的血管生成因子的上调。

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