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树突状细胞 CD73 产生细胞外腺苷对于诱导接触性超敏反应中的耐受至关重要。

Production of Extracellular Adenosine by CD73 Dendritic Cells Is Crucial for Induction of Tolerance in Contact Hypersensitivity Reactions.

机构信息

Department of Dermatology, Ruprecht-Karls-University Heidelberg, Heidelberg, Germany.

Institute for Molecular Cardiology, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.

出版信息

J Invest Dermatol. 2019 Mar;139(3):541-551. doi: 10.1016/j.jid.2018.10.016. Epub 2018 Oct 28.

Abstract

Dendritic cells (DCs) express the ecto-5'-nucleotidase CD73 that generates immunosuppressive adenosine (Ado) by dephosphorylation of extracellular Ado monophosphate and diphosphate. To investigate whether CD73-derived Ado has immune-suppressive activity, 2,4-dinitrothiocyanobenzene (DNTB) was applied to skin of wild-type (WT) or CD73-deficient (CD73) mice, followed by sensitization and challenge with 2,4-dinitrofluorobenzene. In this model, we show the induction of tolerance by DNTB against 2,4-dinitrofluorobenzene only in WT but not in CD73 mice. Analysis of skin DCs showed increased expression of CD73 after application of DNTB in WT mice. That was accompanied by elevated concentrations of extracellular Ado in the lymph node. Moreover, T cells expressed markers for anergy, namely EGR2 and NDRG1 in DNTB-treated WT mice and they exhibited impaired proliferation upon ex vivo re-stimulation. Similarly, in vitro we observed that Ado-producing WT DCs, but not CD73 DCs, rendered transgenic T cells from OTII mice (OTII T cells) hyporeactive, decreased their T-cell costimulatory signaling, and induced up-regulation of EGR2 and NDRG1. Thus, these data show that expression of CD73 by DCs, which triggers elevated levels of extracellular Ado, is a crucial mechanism for the induction of anergic T cells and tolerance.

摘要

树突状细胞 (DCs) 表达ecto-5'-核苷酸酶 CD73,通过磷酸化细胞外腺苷单磷酸和二磷酸的去磷酸化生成免疫抑制性腺苷 (Ado)。为了研究 CD73 衍生的 Ado 是否具有免疫抑制活性,应用 2,4-二硝基硫氰酸苯酯 (DNTB) 于野生型 (WT) 或 CD73 缺陷型 (CD73) 小鼠皮肤,随后用 2,4-二硝基氟苯进行致敏和攻毒。在该模型中,我们发现 DNTB 仅在 WT 小鼠中诱导对 2,4-二硝基氟苯的耐受,而在 CD73 小鼠中则不能。对皮肤 DCs 的分析显示,WT 小鼠 DNTB 处理后 CD73 的表达增加。这伴随着淋巴结中外源性 Ado 浓度的升高。此外,T 细胞在 DNTB 处理的 WT 小鼠中表达无反应性的标志物,即 EGR2 和 NDRG1,并且它们在体外重新刺激时增殖受损。同样,在体外我们观察到产生 Ado 的 WT DCs 但不是 CD73 DCs 使 OTII 小鼠的转基因 T 细胞 (OTII T 细胞) 反应性降低,降低了它们的 T 细胞共刺激信号,并诱导 EGR2 和 NDRG1 的上调。因此,这些数据表明,DCs 表达 CD73,从而引发细胞外 Ado 水平升高,是诱导无反应性 T 细胞和耐受的关键机制。

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