Cerebral organoid research for pediatric patients with neurological disorders.

IF 3.2 Q1 PEDIATRICS
Jin Eun, Jung-Eun Lee, Seung-Ho Yang
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引用次数: 0

Abstract

Cerebral organoids derived from human induced pluripotent stem cells offer a groundbreaking foundation for the analysis of pediatric neurological diseases. Unlike organoids from other somatic systems, cerebral organoids present unique challenges, such as the high sensitivity of neuronal cells to environmental conditions and the complexity of replicating brain-specific architectures. Cerebral organoids replicate the human brain development and pathology, enabling research on conditions such as microcephaly, Rett syndrome, autism spectrum disorders, and brain tumors. This review explores the utility of cerebral organoids for modeling diseases and testing therapeutic interventions. Despite current limitations such as variability and lack of vascularization, recent technological advancements have improved the reliability and application of such interventions. Cerebral organoids provide valuable insight into the mechanisms underlying complex neural disorders and hold promise as novel treatment strategies for pediatric neurological diseases.

小儿神经系统疾病患者脑类器官的研究。
来自人类诱导多能干细胞的脑类器官为儿科神经系统疾病的分析提供了开创性的基础。与来自其他躯体系统的类器官不同,脑类器官面临着独特的挑战,例如神经元细胞对环境条件的高度敏感性以及复制大脑特异性结构的复杂性。脑类器官复制了人类大脑的发育和病理,使小头畸形、Rett综合征、自闭症谱系障碍和脑肿瘤等疾病的研究成为可能。这篇综述探讨了脑类器官在疾病建模和治疗干预测试中的应用。尽管目前存在变异性和缺乏血管化等限制,但最近的技术进步提高了此类干预措施的可靠性和应用。脑类器官为复杂神经疾病的潜在机制提供了有价值的见解,并有望成为儿科神经疾病的新治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.00
自引率
2.40%
发文量
88
审稿时长
60 weeks
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