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病毒标记用于体外和体内靶向单细胞感染。

Virus stamping for targeted single-cell infection in vitro and in vivo.

机构信息

Department of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.

Neural Circuit Laboratories, Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.

出版信息

Nat Biotechnol. 2018 Jan;36(1):81-88. doi: 10.1038/nbt.4034. Epub 2017 Dec 18.

Abstract

Genetic engineering by viral infection of single cells is useful to study complex systems such as the brain. However, available methods for infecting single cells have drawbacks that limit their applications. Here we describe 'virus stamping', in which viruses are reversibly bound to a delivery vehicle-a functionalized glass pipette tip or magnetic nanoparticles in a pipette-that is brought into physical contact with the target cell on a surface or in tissue, using mechanical or magnetic forces. Different single cells in the same tissue can be infected with different viruses and an individual cell can be simultaneously infected with different viruses. We use rabies, lenti, herpes simplex, and adeno-associated viruses to drive expression of fluorescent markers or a calcium indicator in target cells in cell culture, mouse retina, human brain organoid, and the brains of live mice. Virus stamping provides a versatile solution for targeted single-cell infection of diverse cell types, both in vitro and in vivo.

摘要

病毒感染单细胞的基因工程对于研究大脑等复杂系统非常有用。然而,现有的单细胞感染方法存在一些缺陷,限制了它们的应用。在这里,我们描述了“病毒盖章”技术,即将病毒可逆地结合到一个传递载体上,该传递载体是经过功能化处理的玻璃吸管尖端或在吸管中的磁性纳米颗粒,然后通过机械力或磁力与表面或组织中的目标细胞进行物理接触。同一块组织中的不同单细胞可以被不同的病毒感染,并且一个细胞可以同时被不同的病毒感染。我们使用狂犬病病毒、慢病毒、单纯疱疹病毒和腺相关病毒在细胞培养物、小鼠视网膜、人脑类器官和活体小鼠的大脑中的靶细胞中驱动荧光标记物或钙指示剂的表达。病毒盖章为体外和体内多种细胞类型的靶向单细胞感染提供了一种通用的解决方案。

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