嗜粘阿克曼氏菌在疾病调控中的作用。

IF 4.4 2区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Yingying Ding, Yingjian Hou, Xingzhen Lao
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引用次数: 0

摘要

近年来,作为核心肠道共生菌代表的Akkermansia muciniphila (a . muciniphila)由于其独特的粘蛋白降解能力和宿主相互作用机制,在微生态干预领域显示出突出的治疗潜力。嗜粘杆菌于2004年首次从人类粪便中分离出来。它在肠道黏液层定植,利用杯状细胞分泌的粘蛋白作为主要的碳氮来源。2013年,研究人员发现补充A. muciniphila可以改善肥胖,证明A. muciniphila在治疗疾病方面的潜力。最近的研究表明,嗜muciniphila通过多种机制增强肠道屏障完整性,改善代谢疾病,减轻炎症,包括通过toll样受体(TLR) 2刺激腺苷单磷酸活化蛋白激酶(AMPK)途径激活和nod样受体家族,pyrin结构域包含3 (NLRP3)激活。嗜muciniphila及其衍生物也表现出强大的抗肿瘤作用。它们诱导肿瘤坏死因子相关的凋亡诱导配体(TRAIL)上调,触发肿瘤细胞的外源性(死亡受体介导)和内在(线粒体)凋亡途径。此外,嗜muciniphila通过NLRP3激活促进m1样肿瘤相关巨噬细胞(tam),并通过与肿瘤内微生物群的代谢串扰重塑肿瘤微环境。值得注意的是,嗜muciniphila与程序性死亡-1 (PD-1)抗体联合可促进CD8+ T细胞浸润,从而克服宿主对PD-1阻断的抗性。此外,A. muciniphila促进丁酸产菌的生长,抑制特定菌群的生长,在肠道微生物群网络中发挥重要作用。本文综述了嗜粘杆菌在维持肠道屏障完整性、改善代谢和炎症紊乱以及增强抗肿瘤免疫反应等方面的最新发现。本文还讨论了其对肠道菌群的生态作用,指出了其治疗局限性和前景,为促进嗜粘液阿克曼氏菌在临床疾病特别是肿瘤治疗中的发展提供理论参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Role of Akkermansia muciniphila in Disease Regulation.

In recent years, Akkermansia muciniphila (A. muciniphila), as a representative of the core gut commensal bacteria, has shown outstanding therapeutic potential in the field of microecological interventions due to its unique mucin degrading ability and host-interaction mechanism. A. muciniphila is first isolated from human feces in 2004. It colonizes the intestinal mucus layer, utilizing mucin secreted by goblet cells as its primary carbon and nitrogen source. In 2013, researchers found that supplementation with A. muciniphila could improve obesity, demonstrating the potential of A. muciniphila in the treatment of disease. Recent studies show that A. muciniphila strengthens intestinal barrier integrity, improves metabolic diseases, and mitigates inflammation through multiple mechanisms, including adenosine monophosphate-activated protein kinase (AMPK) pathway activation via Toll-like receptor (TLR) 2 stimulation and NOD-like receptor family, pyrin domain containing 3 (NLRP3) activation. A. muciniphila and its derivatives also exhibit potent anti-tumor effects. They induce tumor-necrosis-factor-related apoptosis-inducing ligand (TRAIL) upregulation, triggering extrinsic (death receptor-mediated) and intrinsic (mitochondrial) apoptosis pathways in tumor cells. Additionally, A. muciniphila promotes M1-like tumor-associated macrophages (TAMs) through NLRP3 activation and remodels the tumor microenvironment via metabolic crosstalk with intratumoral microbiota. Notably, A. muciniphila combined with programmed death-1 (PD-1) antibody boost CD8+ T cell infiltration, thereby overcoming host resistance to PD-1 blockade. Moreover, A. muciniphila contributes to the growth of butyric acid-producing bacteria and suppresses the growth of specific bacterial populations, playing an important role in the gut microbiome network. This review evaluates recent discoveries regarding A. muciniphila's multifaceted roles in maintaining intestinal barrier integrity, ameliorating metabolic and inflammatory disorders, and enhancing anti-tumor immune responses. We also discuss its ecological effect on the gut microbiota flora and point out the therapeutic limitations and prospect which provides theoretical references to promote the development of Akkermansia muciniphila in clinical diseases, especially in tumor therapy.

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来源期刊
Probiotics and Antimicrobial Proteins
Probiotics and Antimicrobial Proteins BIOTECHNOLOGY & APPLIED MICROBIOLOGYMICROB-MICROBIOLOGY
CiteScore
11.30
自引率
6.10%
发文量
140
期刊介绍: Probiotics and Antimicrobial Proteins publishes reviews, original articles, letters and short notes and technical/methodological communications aimed at advancing fundamental knowledge and exploration of the applications of probiotics, natural antimicrobial proteins and their derivatives in biomedical, agricultural, veterinary, food, and cosmetic products. The Journal welcomes fundamental research articles and reports on applications of these microorganisms and substances, and encourages structural studies and studies that correlate the structure and functional properties of antimicrobial proteins.
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