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E-NPP3调控小肠中浆细胞样树突状细胞的数量。

E-NPP3 controls plasmacytoid dendritic cell numbers in the small intestine.

作者信息

Furuta Yoki, Tsai Shih-Han, Kinoshita Makoto, Fujimoto Kosuke, Okumura Ryu, Umemoto Eiji, Kurashima Yosuke, Kiyono Hiroshi, Kayama Hisako, Takeda Kiyoshi

机构信息

Laboratory of Immune Regulation, Department of Microbiology and Immunology, Graduate School of Medicine, WPI Immunology Frontier Research Center, Osaka University, Suita, Osaka, Japan.

Core Research for Evolutional Science and Technology, Japan Agency for Medical Research and Development, Tokyo, Japan.

出版信息

PLoS One. 2017 Feb 22;12(2):e0172509. doi: 10.1371/journal.pone.0172509. eCollection 2017.

Abstract

Extracellular adenosine 5'-triphosphate (ATP) performs multiple functions including activation and induction of apoptosis of many cell types. The ATP-hydrolyzing ectoenzyme ecto-nucleotide pyrophosphatase/phosphodiesterase 3 (E-NPP3) regulates ATP-dependent chronic allergic responses by mast cells and basophils. However, E-NPP3 is also highly expressed on epithelial cells of the small intestine. In this study, we showed that E-NPP3 controls plasmacytoid dendritic cell (pDC) numbers in the intestine through regulation of intestinal extracellular ATP. In Enpp3-/- mice, ATP concentrations were increased in the intestinal lumen. pDC numbers were remarkably decreased in the small intestinal lamina propria and Peyer's patches. Intestinal pDCs of Enpp3-/- mice showed enhanced cell death as characterized by increases in annexin V binding and expression of cleaved caspase-3. pDCs were highly sensitive to ATP-induced cell death compared with conventional DCs. ATP-induced cell death was abrogated in P2rx7-/- pDCs. Accordingly, the number of intestinal pDCs was restored in Enpp3-/- P2rx7-/- mice. These findings demonstrate that E-NPP3 regulates ATP concentration and thereby prevents the decrease of pDCs in the small intestine.

摘要

细胞外5'-三磷酸腺苷(ATP)具有多种功能,包括激活和诱导多种细胞类型的凋亡。ATP水解外切酶核苷酸焦磷酸酶/磷酸二酯酶3(E-NPP3)调节肥大细胞和嗜碱性粒细胞依赖ATP的慢性过敏反应。然而,E-NPP3在小肠上皮细胞上也有高表达。在本研究中,我们表明E-NPP3通过调节肠道细胞外ATP来控制肠道中浆细胞样树突状细胞(pDC)的数量。在Enpp3基因敲除小鼠中,肠腔内ATP浓度升高。小肠固有层和派尔集合淋巴结中的pDC数量显著减少。Enpp3基因敲除小鼠的肠道pDC表现出细胞死亡增强,其特征是膜联蛋白V结合增加和裂解的半胱天冬酶-3表达增加。与传统树突状细胞相比,pDC对ATP诱导的细胞死亡高度敏感。ATP诱导的细胞死亡在P2rx7基因敲除的pDC中被消除。因此,Enpp3基因敲除的P2rx7基因敲除小鼠中肠道pDC的数量得以恢复。这些发现表明,E-NPP3调节ATP浓度,从而防止小肠中pDC数量减少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb75/5321438/ce254577dd67/pone.0172509.g001.jpg

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