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Notch 信号通路调控单核细胞来源的朗格汉斯细胞的生成:表型和功能。

Notch-Mediated Generation of Monocyte-Derived Langerhans Cells: Phenotype and Function.

机构信息

Department of Dermatology, Venereology & Allergology, Medical University of Innsbruck, Innsbruck, Austria.

Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.

出版信息

J Invest Dermatol. 2021 Jan;141(1):84-94.e6. doi: 10.1016/j.jid.2020.05.098. Epub 2020 Jun 6.

Abstract

Langerhans cells (LCs) in the skin are a first line of defense against pathogens but also play an essential role in skin homeostasis. Their exclusive expression of the C-type lectin receptor Langerin makes them prominent candidates for immunotherapy. For vaccine testing, an easily accessible cell platform would be desirable as an alternative to the time-consuming purification of LCs from human skin. Here, we present such a model and demonstrate that monocytes in the presence of GM-CSF, TGF-β1, and the Notch ligand DLL4 differentiate within 3 days into CD1aLangerincells containing Birbeck granules. RNA sequencing of these monocyte-derived LCs (moLCs) confirmed gene expression of LC-related molecules, pattern recognition receptors, and enhanced expression of genes involved in the antigen-presenting machinery. On the protein level, moLCs showed low expression of costimulatory molecules but prominent expression of C-type lectin receptors. MoLCs can be matured, secrete IL-12p70 and TNF-α, and stimulate proliferation and cytokine production in allogeneic CD4 and CD8 T cells. In regard to vaccine testing, a recently characterized glycomimetic Langerin ligand conjugated to liposomes demonstrated specific and fast internalization into moLCs. Hence, these short-term in vitro‒generated moLCs represent an interesting tool to screen LC-based vaccines in the future.

摘要

皮肤中的朗格汉斯细胞(LCs)是抵御病原体的第一道防线,但它们在皮肤稳态中也起着至关重要的作用。它们独特地表达 C 型凝集素受体朗格汉斯蛋白,这使它们成为免疫治疗的重要候选者。对于疫苗测试,作为从人皮肤中耗时纯化 LCs 的替代方法,一种易于获得的细胞平台将是理想的选择。在这里,我们提出了这样一种模型,并证明 GM-CSF、TGF-β1 和 Notch 配体 DLL4 存在下的单核细胞在 3 天内分化为含有 Birbeck 颗粒的 CD1aLangerin 细胞。这些单核细胞衍生的 LCs(moLCs)的 RNA 测序证实了与 LC 相关的分子、模式识别受体的基因表达,并增强了与抗原呈递机制相关的基因表达。在蛋白质水平上,moLCs 表现出低水平的共刺激分子表达,但高水平的 C 型凝集素受体表达。moLCs 可以成熟,分泌 IL-12p70 和 TNF-α,并刺激同种异体 CD4 和 CD8 T 细胞的增殖和细胞因子产生。关于疫苗测试,最近表征的一种糖模拟朗格汉斯蛋白配体与脂质体结合,证明其能够特异性和快速内化到 moLCs 中。因此,这些短期在体外生成的 moLCs 代表了未来筛选基于 LCs 的疫苗的一种有趣工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59d0/7758629/c56a4fc7792d/gr1.jpg

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