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An in vivo gene delivery approach for the isolation of reasonable numbers of type 2 innate lymphoid cells

机译:用于分离合理数量的2型先天淋巴细胞的体内基因递送方法

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Group 2 innate lymphoid cells (ILC2s) are a recently recognized subset of innate lymphocytes with crucial role in mucosal immunity and tissue homeostasis. Over the past decade, substantial advances in our understanding of ILC2 biology have established them as an essential element in innate and adaptive immunity. However, their relatively low abundance and laborious purification from mucosal tissues make their study difficult. Moreover, due to a lack of an ILC2-specific Cre mouse-line, adoptive transfer of ILC2s into ILC-deficient hosts is inevitable. Herein we describe an in-depth protocol for the induction, isolation, and expansion of murine ILC2s. By combining an in vivo gene delivery approach to boost ILC2 numbers and a cell culture strategy to expand isolated cells, large quantities of highly pure ILC2s can be obtained. The isolated cells maintain their phenotype and can be used for subsequent cell transfer or in vitro studies. In comparison to previous protocols, this approach is cost-effective and efficient with potential yield of more than 20 million ILC2s isolated per mouse.?Group 2 innate lymphoid cells (ILC2s) are extensively studied in mouse models and humans in recent years.?Low abundance of ILC2s and current lack of specific ILC2 knockout mice makes in vivo research challenging.?This method allows high and pure ILC2 numbers for in vitro or adoptive in vivo transfer experiments.
机译:第2组先天淋巴细胞(ILC2S)是最近认可的先天淋巴细胞子集,具有至关重要的粘膜免疫和组织稳态。在过去十年中,我们对ILC2生物学的理解的大量进步已经建立为先天和适应性免疫的基本要素。然而,它们对粘膜组织的相对较低和富裕的纯化使其研究难以实现。此外,由于缺乏ILC2特异性CRE小鼠线,ILC2S对ILC缺陷宿主的养老液是不可避免的。在此,我们描述了鼠ILC2s的诱导,分离和扩增的深入方案。通过组合体内基因递送方法来增强ILC2数和细胞培养策略以扩张分离的细胞,可以获得大量的高纯ILC2。分离的细胞保持其表型,可用于随后的细胞转移或体外研究。与以前的协议相比,这种方法具有成本效益和高效,潜在的产量超过2000万ILC2S,每小百多于每只小鼠分离。近年来在小鼠模型和人类中广泛研究了先天淋巴细胞(ILC2S)。丰富的ILC2S和目前缺乏特定ILC2敲除小鼠的体内研究挑战性。该方法允许在体内转移实验中体外或养护的高和纯的ILC2号。

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