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建立用于研究小鼠人类免疫功能的反向遗传学系统。

Establishment of a Reverse Genetics System for the Study of Human Immune Functions in Mice.

作者信息

Pal Priya, Gao Shuai, Gao Hongbo, Cella Marina, Wang Qiankun, Shan Liang

出版信息

bioRxiv. 2025 Mar 31:2025.03.26.645295. doi: 10.1101/2025.03.26.645295.

DOI:10.1101/2025.03.26.645295
PMID:40236189
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11996444/
Abstract

Reverse genetics approaches in mice are widely utilized to understand gene functions and their aberrations in diseases. However, limitations exist in translating findings from animal models to human physiology. Humanized mice provide a powerful bridge to understanding human physiology and mechanisms of diseases pathogenesis while maintaining the feasibility of working with small animals. Methods for generating humanized mouse models that allow scientists to probe contributions of particular genes have been rudimentary. Here, we established an efficient method for generating genetically modified human cord blood derived CD34 cells for transplantation, resulting in humanized mice with near-complete loss of specific gene expression by the human immune system. Mice transplanted with Cas9-edited human CD34 cells recapitulate functional consequences of specific gene losses in the human immune system. This advancement enables the development of humanized mouse models with targeted gene knockouts, offering a valuable research tool for human gene function studies .

摘要

小鼠中的反向遗传学方法被广泛用于了解基因功能及其在疾病中的异常。然而,将动物模型的研究结果转化为人类生理学存在局限性。人源化小鼠为理解人类生理学和疾病发病机制提供了一个有力的桥梁,同时保持了使用小动物进行研究的可行性。生成允许科学家探究特定基因贡献的人源化小鼠模型的方法一直很初级。在这里,我们建立了一种有效的方法来生成用于移植的基因编辑人类脐带血来源的CD34细胞,从而产生人源化小鼠,其人类免疫系统中特定基因表达几乎完全丧失。移植了Cas9编辑的人类CD34细胞的小鼠重现了人类免疫系统中特定基因缺失的功能后果。这一进展使得具有靶向基因敲除的人源化小鼠模型得以开发,为人类基因功能研究提供了一个有价值的研究工具。