内质网
未折叠蛋白反应
泛素连接酶
炎症
细胞生物学
化学
脂多糖
泛素
细胞外
内质网相关蛋白降解
受体
信号转导
促炎细胞因子
下调和上调
生物化学
磷酸化
DNA连接酶
酶
酶激活剂
NFKB1型
HEK 293细胞
NF-κB
平衡
刺激1
生物
激酶
内生
作者
Zheng Li,Xuelian Li,Zhou Yu,Qian Fang,Tong Xia,Jiaying Huang,Mingjin Yang,Taoyong Chen
出处
期刊:Science Signaling
[American Association for the Advancement of Science]
日期:2026-07-14
卷期号:19 (946): eaeb2470-eaeb2470
标识
DOI:10.1126/scisignal.aeb2470
摘要
Recognition of the bacterial product lipopolysaccharide (LPS) by Toll-like receptor 4 (TLR4) initiates inflammatory responses. The unfolded protein response (UPR) elicited by endoplasmic reticulum (ER) stress can strengthen TLR4-dependent inflammatory responses. Here, we report that the ER-localized E3 ubiquitin ligase TRIM13 restrained LPS-induced inflammatory responses in macrophages and in mice by protecting the cells from ER stress. TRIM13 mediated Lys 33 -linked polyubiquitylation of the ER-localized Ca 2+ sensor STIM1, promoting its degradation. TRIM13 deficiency caused STIM1 accumulation and activated store-operated Ca 2+ entry (SOCE) and the inositol-requiring enzyme 1 α (IRE1α) branch of the UPR. Suppressing SOCE, chelating extracellular Ca 2+ , relieving ER stress, or blocking IRE1α activation inhibited the amplification of inflammatory responses caused by the loss of TRIM13 in macrophages. Pharmacological inhibition of IRE1α ameliorated chemically induced colitis in TRIM13-deficient mice. Our study suggests that TRIM13 restrains inflammation by limiting LPS-induced activation of SOCE and the IRE1α branch of the UPR.
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