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口服表达α-黑素细胞刺激素的长双歧杆菌以对抗溃疡性结肠炎。

Oral delivery of Bifidobacterium longum expressing α-melanocyte-stimulating hormone to combat ulcerative colitis.

作者信息

Wei Pijin, Yang Yan, Ding Qing, Li Xiuying, Sun Hanxiao, Liu Zhaobing, Huang Junli, Gong Yahui

机构信息

Institute of Genomic Medicine Research, College of Pharmacy, Jinan University, Guangzhou, 510632, PR China.

出版信息

J Med Microbiol. 2016 Feb;65(2):160-168. doi: 10.1099/jmm.0.000197. Epub 2015 Nov 13.

Abstract

α-Melanocyte-stimulating hormone (α-MSH) is a tridecapeptide derived from pro-opiomelanocortin that exhibits potent anti-inflammatory properties by regulating the production of inflammatory mediators. This peptide has been well established in several inflammatory models, including inflammatory bowel disease (IBD). However, its extremely short duration in vivo limits its clinical application. To address this limitation, Bifidobacterium was used here as a carrier to deliver α-MSH. We utilized α-MSH-engineered Bifidobacterium against IBD, which is closely linked to immune and intestinal microbiota dysfunction. First, we constructed a Bifidobacterium longum secreting α-MSH (B. longum-α-MSH). We then tested the recombinant α-MSH expression and determined its bioactivity in HT-29 cells. To assess its effectiveness, B. longum-α-MSH was used against an ulcerative colitis (UC) model in rats induced by dextran sulfate sodium. The data showed that α-MSH expression in B. longum-α-MSH was effective, and its biological activity was similar to the synthesized one. This UC model experiment indicated that B. longum-α-MSH successfully colonized the intestinal gut, expressed bioactive α-MSH and had a significant anti-inflammatory effect. The results demonstrate the feasibility of preventing IBD by using B. longum-α-MSH.

摘要

α-黑素细胞刺激素(α-MSH)是一种由阿黑皮素原衍生而来的十三肽,通过调节炎症介质的产生表现出强大的抗炎特性。该肽在包括炎症性肠病(IBD)在内的多种炎症模型中已得到充分证实。然而,其在体内的作用时间极短,限制了其临床应用。为解决这一局限性,本研究使用双歧杆菌作为载体来递送α-MSH。我们利用工程化表达α-MSH的双歧杆菌来对抗与免疫和肠道微生物群功能障碍密切相关的IBD。首先,我们构建了分泌α-MSH的长双歧杆菌(B. longum-α-MSH)。然后,我们检测了重组α-MSH的表达,并在HT-29细胞中测定了其生物活性。为评估其有效性,将B. longum-α-MSH用于葡聚糖硫酸钠诱导的大鼠溃疡性结肠炎(UC)模型。数据显示,B. longum-α-MSH中α-MSH的表达是有效的,其生物活性与合成的α-MSH相似。该UC模型实验表明,B. longum-α-MSH成功定殖于肠道,表达具有生物活性的α-MSH,并具有显著的抗炎作用。结果证明了使用B. longum-α-MSH预防IBD的可行性。

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