有效冷冻保存人类脑组织和神经器官组织。

IF 4.3 Q1 BIOCHEMICAL RESEARCH METHODS
Cell Reports Methods Pub Date : 2024-05-20 Epub Date: 2024-05-13 DOI:10.1016/j.crmeth.2024.100777
Weiwei Xue, Huijuan Li, Jinhong Xu, Xiao Yu, Linlin Liu, Huihui Liu, Rui Zhao, Zhicheng Shao
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引用次数: 0

摘要

人类脑组织模型和器官组织对于人类神经系统疾病的研究和建模至关重要。然而,长期培养器官组织的高昂成本阻碍了它们的广泛应用。因此,开发低温保存脑组织和器官组织的方法迫在眉睫。在这里,我们建立了一种使用甲基纤维素、乙二醇、二甲基亚砜和 Y27632(称为 MEDY)的方法,用于冷冻保存大脑皮层有机体,而不会破坏神经细胞结构或功能活动。MEDY 可用于多个脑区特异性器官组织,包括背侧/外侧前脑、脊髓、视囊脑和癫痫患者衍生脑器官组织。此外,MEDY 还能冷冻保存人脑组织样本,解冻后仍能保留病理特征。转录组分析表明,MEDY 可以保护突触功能,抑制内质网介导的细胞凋亡途径。MEDY 将实现大规模、可靠地存储各种神经器官组织和活体脑组织,并将促进广泛的研究、医疗应用和药物筛选。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effective cryopreservation of human brain tissue and neural organoids.

Human brain tissue models and organoids are vital for studying and modeling human neurological disease. However, the high cost of long-term cultured organoids inhibits their wide-ranging application. It is therefore urgent to develop methods for the cryopreservation of brain tissue and organoids. Here, we establish a method using methylcellulose, ethylene glycol, DMSO, and Y27632 (termed MEDY) for the cryopreservation of cortical organoids without disrupting the neural cytoarchitecture or functional activity. MEDY can be applied to multiple brain-region-specific organoids, including the dorsal/ventral forebrain, spinal cord, optic vesicle brain, and epilepsy patient-derived brain organoids. Additionally, MEDY enables the cryopreservation of human brain tissue samples, and pathological features are retained after thawing. Transcriptomic analysis shows that MEDY can protect synaptic function and inhibit the endoplasmic reticulum-mediated apoptosis pathway. MEDY will enable the large-scale and reliable storage of diverse neural organoids and living brain tissue and will facilitate wide-ranging research, medical applications, and drug screening.

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来源期刊
Cell Reports Methods
Cell Reports Methods Chemistry (General), Biochemistry, Genetics and Molecular Biology (General), Immunology and Microbiology (General)
CiteScore
3.80
自引率
0.00%
发文量
0
审稿时长
111 days
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