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TonEBP/NFAT5 杂合不足可减轻高脂肪饮食/链脲佐菌素诱导的糖尿病小鼠海马炎症。

TonEBP/NFAT5 haploinsufficiency attenuates hippocampal inflammation in high-fat diet/streptozotocin-induced diabetic mice.

机构信息

Department of Anatomy and Convergence Medical Science, Institute of Health Sciences, Gyeongsang National University School of Medicine, Jinju, Gyeongnam, Republic of Korea.

Bio Anti-aging Medical Research Center, Gyeongsang National University School of Medicine, Jinju, Gyeongnam, Republic of Korea.

出版信息

Sci Rep. 2017 Aug 10;7(1):7837. doi: 10.1038/s41598-017-08319-w.

Abstract

Recent studies have shown that overexpression of tonicity-responsive enhancer binding protein (TonEBP) is associated with many inflammatory diseases, including diabetes mellitus, which causes neuroinflammation in the hippocampus as well as hepatic steatosis. However, the exact mechanism in diabetic neuroinflammation is unknown. We report that haploinsufficiency of TonEBP inhibits hepatic and hippocampal high-mobility group box-1 (HMGB1) expression in diabetic mice. Here, mice were fed a high-fat diet (HFD) for 16 weeks and received an intraperitoneal injection of 100 mg/kg streptozotocin (STZ) and followed by continued HFD feeding for an additional 4 weeks to induce hyperglycemia and hepatic steatosis. Compared with wild-type diabetic mice, diabetic TonEBP mice showed decreased body weight, fat mass, hepatic steatosis, and macrophage infiltration. We also found that adipogenesis and HMGB1 expression in the liver and hippocampus were lower in diabetic TonEBP mice compared with the wild type. Furthermore, iba-1 immunoreactivity in the hippocampus was decreased in diabetic TonEBP mice compared with that in the wild type. Our findings suggest that TonEBP haploinsufficiency suppresses diabetes-associated hepatic steatosis and neuroinflammation.

摘要

最近的研究表明,渗透压反应增强子结合蛋白(TonEBP)的过表达与许多炎症性疾病有关,包括糖尿病,它会导致海马体的神经炎症以及肝脂肪变性。然而,糖尿病性神经炎症的确切机制尚不清楚。我们报告称,TonEBP 的单倍不足抑制了糖尿病小鼠的肝脏和海马体高迁移率族蛋白 B1(HMGB1)的表达。在这里,将小鼠用高脂肪饮食(HFD)喂养 16 周,并进行 100mg/kg 链脲佐菌素(STZ)的腹腔注射,然后继续用 HFD 喂养另外 4 周,以诱导高血糖和肝脂肪变性。与野生型糖尿病小鼠相比,糖尿病 TonEBP 小鼠的体重、脂肪量、肝脂肪变性和巨噬细胞浸润减少。我们还发现,与野生型相比,糖尿病 TonEBP 小鼠的肝脏和海马体中的脂肪生成和 HMGB1 表达降低。此外,与野生型相比,糖尿病 TonEBP 小鼠的海马体中的 iba-1 免疫反应性降低。我们的研究结果表明,TonEBP 的单倍不足抑制了与糖尿病相关的肝脂肪变性和神经炎症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0093/5552681/f86ce51ec993/41598_2017_8319_Fig1_HTML.jpg

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