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巨噬细胞中 RING 手指蛋白 10 的表达减少与衰老相关的炎症有关。

Reduced RING finger protein 10 expression in macrophages is associated with aging-related inflammation.

机构信息

Department of Gastroenterology, Peking Union Medical College Hospital (PUMCH), Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, China.

The Southern Medical District of Chinese PLA General Hospital, Beijing, China.

出版信息

FEBS Open Bio. 2021 Feb;11(2):386-394. doi: 10.1002/2211-5463.13049. Epub 2021 Jan 13.

Abstract

Age-associated decline of the immune system is referred to as immunosenescence. The E3 ligase RING finger 10 (RNF10) has long been associated with the innate immune response, although a potential role in immunosenescence has not previously been reported. In the present study, we identified that RNF10 expression is lower in aged mouse macrophages than in young cells. After lipopolysaccharide stimulation, RNF10 expression remained at a basal low level in aged mouse cells, but declined sharply in young mouse cells. Knockdown of RNF10 enhanced both the nuclear factor-κB and interferon regulatory factor 3 signaling pathways and thus enhanced proinflammatory cytokines and type I interferons in macrophages, promoting clearance of Listeria monocytogenes. These findings indicate that dysregulated expression of RNF10 is associated with age-associated immune dysfunction, and RNF10 may thus be a potential target for the treatment of age-related inflammatory diseases.

摘要

免疫系统随年龄增长而出现的衰退被称为免疫衰老。E3 连接酶 RING 指蛋白 10(RNF10)长期以来一直与先天免疫反应有关,尽管其在免疫衰老中的潜在作用此前尚未被报道。在本研究中,我们发现 RNF10 在衰老的小鼠巨噬细胞中的表达低于年轻细胞。在脂多糖刺激后,RNF10 在衰老的小鼠细胞中的表达仍处于基础的低水平,但在年轻的小鼠细胞中急剧下降。RNF10 的敲低增强了核因子-κB 和干扰素调节因子 3 信号通路,从而增强了巨噬细胞中的促炎细胞因子和 I 型干扰素,促进了李斯特菌的清除。这些发现表明,RNF10 的表达失调与年龄相关的免疫功能障碍有关,因此 RNF10 可能是治疗与年龄相关的炎症性疾病的潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af3c/7876489/a9e835817adc/FEB4-11-386-g001.jpg

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