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移植到中风损伤大鼠纹状体中的人胎儿纹状体和皮质神经干细胞的存活、迁移及神经元分化

Survival, migration and neuronal differentiation of human fetal striatal and cortical neural stem cells grafted in stroke-damaged rat striatum.

作者信息

Darsalia Vladimer, Kallur Therése, Kokaia Zaal

机构信息

Laboratory of Neural Stem Cell Biology, Section of Restorative Neurology, Lund Strategic Research Center for Stem Cell Biology and Cell Therapy, University Hospital BMC B10, Klinikgatan 26, SE-221 84 Lund, Sweden.

出版信息

Eur J Neurosci. 2007 Aug;26(3):605-14. doi: 10.1111/j.1460-9568.2007.05702.x.

Abstract

Stroke is a neurodegenerative disorder and the leading cause of disability in adult humans. Treatments to support efficient recovery in stroke patients are lacking. Several studies have demonstrated the ability of grafted neural stem cells (NSCs) to partly improve impaired neurological functions in stroke-subjected animals. Recently, we reported that NSCs from human fetal striatum and cortex exhibit region-specific differentiation in vitro, but survive, migrate and form neurons to a similar extent after intrastriatal transplantation in newborn rats. Here, we have transplanted the same cells into the stroke-damaged striatum of adult rats. The two types of NSCs exhibited a similar robust survival (30%) at 1 month after transplantation, and migrated throughout the damaged striatum. Striatal NSCs migrated farther and occupied a larger volume of striatum. In the transplantation core, cells were undifferentiated and expressed nestin and, to a lesser extent, also GFAP, betaIII-tubulin, DCX and calretinin, markers of immature neural lineage. Immunocytochemistry using markers of proliferation (p-H3 and Ki67) revealed a very low content of proliferating cells (<1%) in the grafts. Human cells outside the transplantation core differentiated, exhibited mature neuronal morphology and expressed mature neuronal markers such as HuD, calbindin and parvalbumin. Interestingly, striatal NSCs generated a greater number of parvalbumin+ and calbindin+ neurons. Virtually none of the grafted cells differentiated into astrocytes or oligodendrocytes. Based on these data, human fetal striatum- and cortex-derived NSCs could be considered potentially safe and viable for transplantation, with strong neurogenic potential, for further exploration in animal models of stroke.

摘要

中风是一种神经退行性疾病,也是成年人残疾的主要原因。目前缺乏支持中风患者有效康复的治疗方法。多项研究已证明,移植的神经干细胞(NSC)能够部分改善中风动物受损的神经功能。最近,我们报道了来自人类胎儿纹状体和皮质的NSC在体外表现出区域特异性分化,但在新生大鼠纹状体内移植后,它们的存活、迁移以及形成神经元的程度相似。在此,我们将相同的细胞移植到成年大鼠中风损伤的纹状体中。两种类型的NSC在移植后1个月均表现出相似的高存活率(30%),并迁移至整个受损纹状体。纹状体NSC迁移得更远,占据的纹状体体积更大。在移植核心区域,细胞未分化,表达巢蛋白,在较小程度上也表达GFAP、βIII微管蛋白、双皮质素和钙视网膜蛋白,这些都是未成熟神经谱系的标志物。使用增殖标志物(p-H3和Ki67)进行免疫细胞化学分析显示,移植物中增殖细胞的含量极低(<1%)。移植核心区域外的人类细胞发生分化,呈现出成熟的神经元形态,并表达成熟的神经元标志物,如HuD、钙结合蛋白和小白蛋白。有趣的是,纹状体NSC产生了更多的小白蛋白阳性和钙结合蛋白阳性神经元。几乎没有移植细胞分化为星形胶质细胞或少突胶质细胞。基于这些数据,来自人类胎儿纹状体和皮质的NSC在中风动物模型中具有很强的神经发生潜力,可被认为可能是安全且可行的移植对象,有待进一步探索。

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