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NUCB2/Nesfatin-1 可减轻肥胖饮食诱导的小鼠皮下白色脂肪组织炎症。

NUCB2/Nesfatin-1 Reduces Obesogenic Diet Induced Inflammation in Mice Subcutaneous White Adipose Tissue.

机构信息

Warwickshire Institute for the Study of Diabetes, Endocrinology and Metabolism (WISDEM), University Hospitals Coventry and Warwickshire NHS Trust, Coventry CV2 2DX, UK.

Warwick Medical School, University of Warwick, Coventry CV4 7AL, UK.

出版信息

Nutrients. 2022 Mar 28;14(7):1409. doi: 10.3390/nu14071409.

Abstract

BACKGROUND

Excess adipose tissue accumulation and obesity are characterised by chronic, low-grade, systemic inflammation. Nestfatin-1 is a neuropeptide derived from the precursor protein nucleobindin-2 (NUCB2), which was initially reported to exert anorexigenic effects. The present study aimed to investigate the effects of an obesogenic diet (OD; high-fat, high-sugar) in NUCB2 knockout (KO) mice and of nesfatin-1 treatment in LPS-stimulated 3T3-L1 preadipocytes.

METHODS

Subcutaneous white adipose tissue (Sc-WAT) samples from wild type (WT) and NUCB2 KO mice that were fed a normal diet (ND), or the OD for 12 weeks were used for RNA and protein extraction, as well as immunohistochemistry. 3T3-L1 cells were treated with 100 nM nesfatin-1 during differentiation and stimulated with 1 µg/mL LPS for measuring the expression and secretion of pro-inflammatory mediators by qPCR, western blotting, immunofluorescence, Bioplex, and ELISA.

RESULTS

Following the OD, the mRNA, protein and cellular expression of pro-inflammatory mediators (Tnfα, Il-6, Il-1β, Adgre1, Mcp1, TLR4, Hmbgb1 and NF-kB) significantly increased in the ScWAT of NUCB2 KO mice compared to ND controls. Adiponectin and Nrf2 expression significantly decreased in the ScWAT of OD-fed NUCB2 KO, without changes in the OD-fed WT mice. Furthermore, nesfatin-1 treatment in LPS-stimulated 3T3-L1 cells significantly reduced the expression and secretion of pro-inflammatory cytokines (Tnfα, Il-6, Il-1β, Mcp1) and hmgb1.

CONCLUSION

An obesogenic diet can induce significant inflammation in the ScWAT of NUCB2 KO mice, involving the HMGB1, NRF2 and NF-kB pathways, while nesfatin-1 reduces the pro-inflammatory response in LPS-stimulated 3T3-L1 cells. These findings provide a novel insight into the metabolic regulation of inflammation in WAT.

摘要

背景

过多的脂肪组织积累和肥胖的特点是慢性、低度、全身性炎症。内脂素-1 是一种源自核结合蛋白-2(NUCB2)前体蛋白的神经肽,最初报道具有厌食作用。本研究旨在探讨肥胖饮食(OD;高脂肪、高糖)对 NUCB2 敲除(KO)小鼠和 LPS 刺激的 3T3-L1 前体脂肪细胞中内脂素-1 治疗的影响。

方法

用正常饮食(ND)或 OD 喂养 12 周的野生型(WT)和 NUCB2 KO 小鼠的皮下白色脂肪组织(Sc-WAT)样本进行 RNA 和蛋白质提取以及免疫组织化学分析。在分化过程中用 100 nM 内脂素-1 处理 3T3-L1 细胞,并以 1 µg/mL LPS 刺激,通过 qPCR、western blot、免疫荧光、Bioplex 和 ELISA 测量促炎介质的表达和分泌。

结果

OD 后,与 ND 对照组相比,NUCB2 KO 小鼠 ScWAT 中促炎介质(Tnfα、Il-6、Il-1β、Adgre1、Mcp1、TLR4、Hmbgb1 和 NF-kB)的 mRNA、蛋白和细胞表达显著增加。脂联素和 Nrf2 的表达在 OD 喂养的 NUCB2 KO 小鼠的 ScWAT 中显著降低,而在 OD 喂养的 WT 小鼠中没有变化。此外,LPS 刺激的 3T3-L1 细胞中内脂素-1 的治疗显著降低了促炎细胞因子(Tnfα、Il-6、Il-1β、Mcp1)和 hmgb1 的表达和分泌。

结论

肥胖饮食可诱导 NUCB2 KO 小鼠 ScWAT 发生显著炎症,涉及 HMGB1、NRF2 和 NF-kB 途径,而内脂素-1 可降低 LPS 刺激的 3T3-L1 细胞中的促炎反应。这些发现为 WAT 中炎症的代谢调节提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d22/9003550/e239b370496c/nutrients-14-01409-g001.jpg

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