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利用基质细胞培养进行人树突状细胞前体细胞的克隆分析。

Clonal Analysis of Human Dendritic Cell Progenitors Using a Stromal Cell Culture.

机构信息

Cancer Immunology and Immune Modulation, Boehringer Ingelheim, Ridgefield, CT, USA.

Memorial Sloan Kettering Cancer Center, New York, NY, USA.

出版信息

Methods Mol Biol. 2023;2618:155-170. doi: 10.1007/978-1-0716-2938-3_12.

Abstract

Dendritic cells (DCs) are a heterogenous population of professional antigen-presenting cells that play an "educator" role in immunity. Multiple DC subsets collaboratively initiate and orchestrate innate and adaptive immune responses. Recent advances in our ability to investigate cellular transcription, signaling, and function at the single-cell level have opened opportunities to examine heterogeneous populations at unprecedented resolutions. Culturing of mouse DC subsets from single bone marrow hematopoietic progenitor cells, that is, clonal analysis, has enabled identification of multiple progenitors with distinct potentials and furthered understanding of mouse DC development. However, studies of human DC development have been hampered by the lack of a corresponding system to generate multiple human DC subsets. Here, we describe a protocol to functionally profile the differentiation potentials of single human hematopoietic stem and progenitor cells (HSPCs) to multiple DC subsets, myeloid and lymphoid cells that will facilitate investigation of human DC lineage specification and reveal its molecular bases.

摘要

树突状细胞(DCs)是一类异质性的专业抗原呈递细胞,在免疫中发挥“教育者”的作用。多个 DC 亚群协同启动和协调先天和适应性免疫反应。我们在单细胞水平上研究细胞转录、信号和功能的能力的最新进展为以前所未有的分辨率检查异质群体提供了机会。从单个骨髓造血祖细胞培养小鼠 DC 亚群,即克隆分析,已经能够鉴定出具有不同潜能的多个祖细胞,并进一步了解小鼠 DC 的发育。然而,由于缺乏生成多种人类 DC 亚群的相应系统,人类 DC 发育的研究受到了阻碍。在这里,我们描述了一种方案,用于对单个人类造血干/祖细胞(HSPCs)向多个 DC 亚群、髓系和淋巴系细胞的分化潜能进行功能分析,这将有助于研究人类 DC 谱系的特化,并揭示其分子基础。

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