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Ikaros 家族锌指蛋白 1 调节人类树突状细胞的发育和功能。

Ikaros family zinc finger 1 regulates dendritic cell development and function in humans.

机构信息

Institute of Cellular Medicine, Newcastle University, Framlington Place, Newcastle upon Tyne, NE2 4HH, UK.

Primary Immunodeficiency Research Lab, Department of Pulmonary Medicine, Ghent University Hospital, C. Heymanslaan 10, 9000, Ghent, Belgium.

出版信息

Nat Commun. 2018 Mar 27;9(1):1239. doi: 10.1038/s41467-018-02977-8.

Abstract

Ikaros family zinc finger 1 (IKZF1) is a haematopoietic transcription factor required for mammalian B-cell development. IKZF1 deficiency also reduces plasmacytoid dendritic cell (pDC) numbers in mice, but its effects on human DC development are unknown. Here we show that heterozygous mutation of IKZF1 in human decreases pDC numbers and expands conventional DC1 (cDC1). Lenalidomide, a drug that induces proteosomal degradation of IKZF1, also decreases pDC numbers in vivo, and reduces the ratio of pDC/cDC1 differentiated from progenitor cells in vitro in a dose-dependent manner. In addition, non-classical monocytes are reduced by IKZF1 deficiency in vivo. DC and monocytes from patients with IKZF1 deficiency or lenalidomide-treated cultures secrete less IFN-α, TNF and IL-12. These results indicate that human DC development and function are regulated by IKZF1, providing further insights into the consequences of IKZF1 mutation on immune function and the mechanism of immunomodulation by lenalidomide.

摘要

Ikaros 家族锌指蛋白 1(IKZF1)是一种造血转录因子,对于哺乳动物 B 细胞的发育是必需的。IKZF1 的缺失也会减少小鼠中浆细胞样树突状细胞(pDC)的数量,但它对人类树突状细胞(DC)发育的影响尚不清楚。在这里,我们发现人类 IKZF1 的杂合突变会减少 pDC 的数量,并扩增常规 DC1(cDC1)。来那度胺,一种诱导 IKZF1 蛋白体降解的药物,也会在体内减少 pDC 的数量,并以剂量依赖的方式减少体外由祖细胞分化而来的 pDC/cDC1 的比例。此外,体内 IKZF1 缺失会减少非经典单核细胞。来自 IKZF1 缺失或来那度胺处理培养物的 DC 和单核细胞分泌的 IFN-α、TNF 和 IL-12 减少。这些结果表明,人类 DC 的发育和功能受到 IKZF1 的调节,为 IKZF1 突变对免疫功能的影响以及来那度胺的免疫调节机制提供了进一步的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4816/5869589/6102f74ddd5f/41467_2018_2977_Fig1_HTML.jpg

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