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Impact of age on the efficacy of bone marrow mononuclear cell transplantation in experimental stroke

机译:年龄对实验性卒中骨髓单核细胞移植疗效的影响

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Bone marrow-derived mononuclear cells (BM MNC) have been effectively used to treat experimental stroke. Most of the preclinical trials have been performed in young and healthy laboratory animals, even though age and hypertension are major risk factors for stroke. To determine the influence of age on the properties of BM MNCs after cerebral ischemia, we compared the efficacy of aged and young BM MNC in an in vitro model of cerebral hypoxia and in an adapted in vivo model of stroke. Human BM MNCs were obtained from healthy young or aged donors and either co-cultured with rat hippocampal slices exposed to oxygen glucose deprivation (OGD), or transplanted intravenously 24 h after permanent middle cerebral artery occlusion in aged (18 months) spontaneously hypertensive rats (SHR). Efficacy was examined by quantification of hippocampal cell death, or respectively, by neurofunctional tests and MR investigations. Co-cultivation with young, but not with aged BM MNCs significantly reduced the hippocampal cell death after OGD. Transplantation of both young and old BM MNCs did not reduce functional deficits or ischemic lesion volume after stroke in aged SHR. These results suggest a significant impact of age on the therapeutic efficacy of BM MNCs after cerebral ischemia.
机译:骨髓来源的单核细胞(BM MNC)已被有效地用于治疗实验性中风。尽管年龄和高血压是中风的主要危险因素,但大多数临床前试验都是在年轻健康的实验动物中进行的。为了确定年龄对脑缺血后BM MNCs属性的影响,我们比较了老年和年轻BM MNC在脑缺氧的体外模型和中风的体内模型中的功效。人类BM MNCs来自健康的年轻或老年供体,或者与暴露于缺氧葡萄糖(OGD)的大鼠海马切片共培养,或者在年龄较大(18个月)的自发性高血压大鼠中,永久性大脑中动脉闭塞后24小时静脉内移植( SHR)。通过定量海马细胞死亡或通过神经功能测试和MR研究分别检查疗效。与年轻但不与老年BM MNC共同培养可显着降低OGD后海马细胞死亡。老年SHR的年轻和老年BM MNC移植均未减少其功能缺陷或缺血性病变体积。这些结果表明年龄对脑缺血后BM MNC的治疗效果有重大影响。

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