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

长双歧杆菌 溃疡性结肠炎 双歧杆菌 炎症性肠病 结肠炎 免疫系统 促黑素细胞激素 医学 免疫学 激素 生物 内科学 细菌 疾病 乳酸菌 遗传学
作者
Pijin Wei,Yan Yang,Qing Ding,Xiuying Li,Hanxiao Sun,Zhaobing Liu,Junli Huang,Yahui Gong
出处
期刊:Journal of Medical Microbiology [Microbiology Society]
卷期号:65 (2): 160-168 被引量:37
标识
DOI:10.1099/jmm.0.000197
摘要

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.
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