Alcohol induces α2-6sialo mucin O-glycans that kill U937 macrophages mediated by sialic acid-binding immunoglobulin-like lectin 7 (Siglec 7)

IF 2.8 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Pi-Wan Cheng, Vishwanath-Reddy Hothpet, Ganapati Bhat, Kristina Bailey, Lei Li, Derrick R. Samuelson
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引用次数: 0

Abstract

Alcohol misuse increases infections and cancer fatalities, but mechanisms underlying its toxicity are ill-defined. We show that alcohol treatment of human tracheobronchial epithelial cells leads to inactivation of giantin-mediated Golgi targeting of glycosylation enzymes. Loss of core 2 N-acetylglucosaminyltransferase 1, which uses only giantin for Golgi targeting, coupled with shifted targeting of other glycosylation enzymes to Golgi matrix protein 130-Golgi reassembly stacking protein 65, the site normally used by core 1 enzyme, results in loss of sialyl Lewis x and increase of sialyl Lewis a and α2-6sialo mucin O-glycans. The α2-6sialo mucin O-glycans induced by alcohol cause death of U937 macrophages mediated by sialic acid-binding immunoglobulin-like lectin 7. These results provide a mechanistic insight into the cause of the toxic effects of alcohol and might contribute to the development of therapies to alleviate its toxicity.

Abstract Image

酒精会诱导α2-6sialo粘蛋白O-糖,这种粘蛋白O-糖可通过与硅谷酸结合的免疫球蛋白样凝集素7(Siglec 7)杀死U937巨噬细胞。
滥用酒精会增加感染和癌症死亡率,但其毒性机制尚不明确。我们的研究表明,酒精处理人类气管支气管上皮细胞会导致巨蛋白介导的高尔基体糖基化酶靶向失活。核心 2 N-乙酰葡糖胺基转移酶 1 只使用巨球蛋白进行高尔基体靶向,而其他糖基化酶的靶向转移到了高尔基体基质蛋白 130-高尔基体重组堆积蛋白 65(核心 1 酶通常使用的位点),核心 2 N-乙酰葡糖胺基转移酶 1 的缺失导致硅氨酰路易斯 x 的缺失,而硅氨酰路易斯 a 和α2-6sialo 粘蛋白 O-糖的增加。酒精诱导的α2-6sialo 粘蛋白 O-聚糖会导致 U937 巨噬细胞在硅氨酰基结合免疫球蛋白样凝集素 7 的介导下死亡。这些结果从机理上揭示了酒精毒性作用的原因,可能有助于开发减轻酒精毒性的疗法。
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来源期刊
FEBS Open Bio
FEBS Open Bio BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
5.10
自引率
0.00%
发文量
173
审稿时长
10 weeks
期刊介绍: FEBS Open Bio is an online-only open access journal for the rapid publication of research articles in molecular and cellular life sciences in both health and disease. The journal''s peer review process focuses on the technical soundness of papers, leaving the assessment of their impact and importance to the scientific community. FEBS Open Bio is owned by the Federation of European Biochemical Societies (FEBS), a not-for-profit organization, and is published on behalf of FEBS by FEBS Press and Wiley. Any income from the journal will be used to support scientists through fellowships, courses, travel grants, prizes and other FEBS initiatives.
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