适配蛋白3BP2除了在Dectin-1刺激的细胞中调节MALT1的泛素化和蛋白水解活性外,还调节基因表达。

IF 4 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Biological Chemistry Pub Date : 2024-11-12 DOI:10.1016/j.jbc.2024.107980
Ayumi Tsubokawa, Kazuyasu Chihara, Yuri Chihara, Kenji Takeuchi, Shigeharu Fujieda, Kiyonao Sada
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引用次数: 0

摘要

Dectin-1是一种C型凝集素,在诱导抗真菌免疫中发挥着重要作用。Caspase recruitment domain-containing protein 9(CARD9)是通过激活 NF-κB 由 Dectin-1 诱导产生细胞因子的关键。然而,Dectin-1 介导的 CARD9 激活的分子机制尚未完全阐明。最近,我们报道了适配蛋白 SH3 结构域结合蛋白 2(3BP2)是 dectin-1 诱导细胞因子产生和 NF-κB 活化所必需的,但 3BP2 和 CARD9 在 dectin-1 介导的信号转导中的关系仍不清楚。在这里,我们报告了 3BP2 是 dectin-1 诱导的多个基因表达所必需的,这些基因可能有助于骨髓树突状细胞(BMDCs)的抗真菌免疫。使用 HEK-293T 细胞进行的报告实验结果表明,3BP2 通过 B 细胞白血病/淋巴瘤 10、粘膜相关淋巴组织淋巴瘤转位蛋白 1(MALT1)和 TNF 受体相关因子 6 依赖性机制诱导 CARD9 介导的 NF-κB 激活。此外,我们还发现 3BP2 可诱导 CARD9 介导的细胞蛋白泛素化,并且 MALT1 会以依赖 CARD9 的方式裂解 3BP2。此外,我们还发现,除了激活 MALT1 外,3BP2 也需要泛素化,这就导致了 MALT1 依赖性地裂解 dectin-1 刺激的 BMDCs 中的 3BP2。最后,我们发现造血细胞特异性 Lyn 底物 1 是 3BP2 的靶标,它对 dectin-1 诱导的白细胞介素 10 在 BMDCs 中的表达至关重要。这些结果表明,3BP2 可调控八肽-1 刺激的细胞中 MALT1 的基因表达和功能,并且 3BP2 在八肽-1 介导的抗真菌免疫中发挥着重要作用。
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Adaptor protein 3BP2 regulates gene expression in addition to the ubiquitination and proteolytic activity of MALT1 in dectin-1-stimulated cells.

Dectin-1, a C-type lectin, plays important roles in the induction of antifungal immunity. Caspase recruitment domain-containing protein 9 (CARD9) is essential for the dectin-1-induced production of cytokines through the activation of NF-κB. However, the molecular mechanisms underlying the dectin-1-mediated activation of CARD9 have not been fully elucidated. Recently, we reported that the adaptor protein SH3 domain-binding protein 2 (3BP2) is required for the dectin-1-induced production of cytokines and activation of NF-κB, although the relationship between 3BP2 and CARD9 in dectin-1-mediated signaling remains unclear. Here, we report that 3BP2 is required for dectin-1-induced expression of several genes that may contribute to antifungal immunity in bone marrow-derived dendritic cells (BMDCs). The results of reporter assays using HEK-293T cells indicate that 3BP2 induces CARD9-mediated activation of NF-κB through B-cell leukemia/lymphoma 10, mucosa-associated lymphoid tissue lymphoma translocation protein 1 (MALT1), and TNF receptor-associated factor 6-dependent mechanisms. In addition, we show that 3BP2 induces CARD9-mediated ubiquitination of cellular proteins and that MALT1 cleaves 3BP2 in a CARD9-dependent manner. Furthermore, we show that 3BP2 is required for the ubiquitination, in addition to the activation, of MALT1, which leads to MALT1-depenedent cleavage of 3BP2 in dectin-1-stimulated BMDCs. Finally, we identified hematopoietic cell-specific Lyn substrate 1 as a target of 3BP2, which is essential for dectin-1-induced expression of interleukin 10 in BMDCs. These results indicate that 3BP2 regulates gene expression and functions of MALT1 in dectin-1-stimulated cells and that 3BP2 plays an important role in the dectin-1-mediated antifungal immunity.

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Journal of Biological Chemistry
Journal of Biological Chemistry Biochemistry, Genetics and Molecular Biology-Biochemistry
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期刊介绍: The Journal of Biological Chemistry welcomes high-quality science that seeks to elucidate the molecular and cellular basis of biological processes. Papers published in JBC can therefore fall under the umbrellas of not only biological chemistry, chemical biology, or biochemistry, but also allied disciplines such as biophysics, systems biology, RNA biology, immunology, microbiology, neurobiology, epigenetics, computational biology, ’omics, and many more. The outcome of our focus on papers that contribute novel and important mechanistic insights, rather than on a particular topic area, is that JBC is truly a melting pot for scientists across disciplines. In addition, JBC welcomes papers that describe methods that will help scientists push their biochemical inquiries forward and resources that will be of use to the research community.
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