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Aging in a Dish: iPSC-Derived and Directly Induced Neurons for Studying Brain Aging and Age-Related Neurodegenerative Diseases

机译:在一道菜中的老化:IPSC衍生的和直接诱导学习脑老化和年龄相关神经变性疾病的神经元

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Age-associated neurological diseases represent a profound challenge in biomedical research as we are still struggling to understand the interface between the aging process and the manifestation of disease. Various pathologies in the elderly do not directly result from genetic mutations, toxins, or infectious agents but are primarily driven by the many manifestations of biological aging. Therefore, the generation of appropriate model systems to study human aging in the nervous system demands new concepts that lie beyond transgenic and drug-induced models. Although access to viable human brain specimens is limited and induced pluripotent stem cell models face limitations due to reprogramming-associated cellular rejuvenation, the direct conversion of somatic cells into induced neurons allows for the generation of human neurons that capture many aspects of aging. Here, we review advances in exploring age-associated neurodegenerative diseases using human cell reprogramming models, and we discuss general concepts, promises, and limitations of the field.
机译:年龄相关的神经系统疾病在生物医学研究中代表了深刻的挑战,因为我们仍在努力了解老化过程与疾病的表现之间的界面。老年人的各种病理学不会直接由遗传突变,毒素或传染性剂导致,而是主要由生物老化的许多表现因素引起。因此,在神经系统中研究人类衰老的适当模型系统需要围绕转基因和药物诱导的模型的新概念。尽管获得可行的人脑样本是有限的,并且诱导多能干细胞模型由于重编程相关的细胞再活化而面临限制,但是体细胞的直接转化为诱导的神经元允许产生捕获老化的许多方面的人神经元。在这里,我们审查使用人体细胞重编程模型探索年龄相关的神经退行性疾病的进步,我们讨论了该领域的一般概念,承诺和局限性。

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