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中风后诱导多能干细胞的治疗潜力:来自啮齿动物模型的证据。

The Therapeutic Potential of Induced Pluripotent Stem Cells After Stroke: Evidence from Rodent Models.

作者信息

Zents Karlijn, Copray Sjef

机构信息

Department of Neuroscience, University Medical Centre Groningen, University of Groningen, A.Deusinglaan 1 9713AV Groningen, The Netherlands.

出版信息

Curr Stem Cell Res Ther. 2016;11(2):166-74. doi: 10.2174/1574888x10666150728121324.

Abstract

Stroke is the second most common cause of death and the leading cause of disability in the world. About 30% of the people that are affected by stroke die within a year; 25% of the patients that survive stroke remain in need of care after a year. Therefore, stroke is a major burden for health care costs. The most common subtype is ischemic stroke. This type is characterized by a reduced and insufficient blood supply to a certain part of the brain. Despite the high prevalence of stroke, the currently used therapeutic interventions are limited. No therapies that aim to restore damaged neuronal tissue or to promote recovery are available nowadays. Transplantation of stem cell-derived cells has been investigated as a potential regenerative and protective treatment. Embryonic stem cell (ESC)-based cell therapy in rodent models of stroke has been shown to improve functional outcome. However, the clinical use of ESCs still raises ethical questions and implantation of ESC-derived cells requires continuous immunosuppression. The groundbreaking detection of induced pluripotent stem cells (iPSCs) has provided a most promising alternative. This mini-review summarizes current literature in which the potential use of iPSC-derived cells has been tested in rodent models of stroke. iPSC-based cell therapy has been demonstrated to improve motor function, decrease stroke volume, promote neurogenesis and angiogenesis and to exert immunomodulatory, anti-inflammatory effects in the brain of stroke-affected rodents.

摘要

中风是全球第二大常见死因和致残的主要原因。约30%的中风患者在一年内死亡;中风幸存者中有25%在一年后仍需要护理。因此,中风是医疗费用的一项重大负担。最常见的亚型是缺血性中风。这种类型的特点是大脑某一部位的血液供应减少且不足。尽管中风的患病率很高,但目前使用的治疗干预措施有限。目前尚无旨在修复受损神经元组织或促进恢复的疗法。干细胞衍生细胞的移植已作为一种潜在的再生和保护性治疗方法进行了研究。在中风的啮齿动物模型中,基于胚胎干细胞(ESC)的细胞疗法已被证明可改善功能结局。然而,ESC的临床应用仍然引发伦理问题,并且植入ESC衍生细胞需要持续的免疫抑制。诱导多能干细胞(iPSC)的突破性发现提供了一个最有前景的替代方案。这篇小型综述总结了当前的文献,其中iPSC衍生细胞的潜在用途已在中风的啮齿动物模型中进行了测试。基于iPSC的细胞疗法已被证明可改善运动功能、减少中风体积、促进神经发生和血管生成,并在中风影响的啮齿动物大脑中发挥免疫调节、抗炎作用。

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