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诱导宿主中促进其存活的表观遗传机制。

Epigenetic Mechanisms Induced by to Promote Its Survival in the Host.

机构信息

School of Biotechnology, Amrita Vishwa Vidyapeetham, Amritapuri, Kollam 690525, Kerala, India.

Department of Life Sciences, CHRIST (Deemed to be University), Bangalore 560029, Karnataka, India.

出版信息

Int J Mol Sci. 2024 Nov 2;25(21):11801. doi: 10.3390/ijms252111801.

DOI:10.3390/ijms252111801
PMID:39519352
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11546203/
Abstract

Tuberculosis caused by the obligate intracellular pathogen, , is one among the prime causes of death worldwide. An urgent remedy against tuberculosis is of paramount importance in the current scenario. However, the complex nature of this appalling disease contributes to the limitations of existing medications. The quest for better treatment approaches is driving the research in the field of host epigenomics forward in context with tuberculosis. The interplay between various host epigenetic factors and the pathogen is under investigation. A comprehensive understanding of how orchestrates such epigenetic factors and favors its survival within the host is in increasing demand. The modifications beneficial to the pathogen are reversible and possess the potential to be better targets for various therapeutic approaches. The mechanisms, including histone modifications, DNA methylation, and miRNA modification, are being explored for their impact on pathogenesis. In this article, we are deciphering the role of mycobacterial epigenetic regulators on various strategies like cytokine expression, macrophage polarization, autophagy, and apoptosis, along with a glimpse of the potential of host-directed therapies.

摘要

结核分枝杆菌是一种专性细胞内病原体,是全球主要死亡原因之一。在当前情况下,迫切需要一种针对结核病的治疗方法。然而,这种可怕疾病的复杂性导致了现有药物的局限性。为了寻找更好的治疗方法,宿主表观基因组学领域的研究正在向前推进。目前正在研究各种宿主表观遗传因子与病原体之间的相互作用。越来越需要深入了解结核分枝杆菌如何协调这些表观遗传因子并有利于其在宿主内的存活。对病原体有益的修饰是可逆的,有可能成为各种治疗方法的更好靶点。包括组蛋白修饰、DNA 甲基化和 miRNA 修饰在内的机制正在被探索,以了解它们对发病机制的影响。在本文中,我们正在破译分枝杆菌表观遗传调节剂在细胞因子表达、巨噬细胞极化、自噬和细胞凋亡等各种策略中的作用,同时也探讨了宿主定向治疗的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/009e/11546203/ef66b211974b/ijms-25-11801-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/009e/11546203/f101d46bc26b/ijms-25-11801-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/009e/11546203/ef66b211974b/ijms-25-11801-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/009e/11546203/f101d46bc26b/ijms-25-11801-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/009e/11546203/ef66b211974b/ijms-25-11801-g002.jpg

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本文引用的文献

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Downregulation of monocyte miRNAs: implications for immune dysfunction and disease severity in drug-resistant tuberculosis.下调单核细胞 miRNA:对耐药性结核病免疫功能障碍和疾病严重程度的影响。
Front Immunol. 2023 Jun 29;14:1197805. doi: 10.3389/fimmu.2023.1197805. eCollection 2023.
2
Antimicrobial resistance and mechanisms of epigenetic regulation.抗微生物耐药性和表观遗传调控机制。
Front Cell Infect Microbiol. 2023 Jun 14;13:1199646. doi: 10.3389/fcimb.2023.1199646. eCollection 2023.
3
How epigenetics impacts on human diseases.
表观遗传学如何影响人类疾病。
Eur J Intern Med. 2023 Aug;114:15-22. doi: 10.1016/j.ejim.2023.05.036. Epub 2023 Jun 3.
4
Epigenetic orchestration of host immune defences by Mycobacterium tuberculosis.结核分枝杆菌对宿主免疫防御的表观遗传调控。
Microbiol Res. 2023 Aug;273:127400. doi: 10.1016/j.micres.2023.127400. Epub 2023 May 3.
5
Sirtuin-dependent metabolic and epigenetic regulation of macrophages during tuberculosis.结核菌感染期间巨噬细胞中依赖于 Sirtuin 的代谢和表观遗传调控。
Front Immunol. 2023 Mar 13;14:1121495. doi: 10.3389/fimmu.2023.1121495. eCollection 2023.
6
Mycobacterial protein PE_PGRS30 induces macrophage apoptosis through prohibitin 2 mitochondrial function interference.分枝杆菌蛋白PE_PGRS30通过干扰抑癌蛋白2的线粒体功能诱导巨噬细胞凋亡。
Front Microbiol. 2023 Jan 27;14:1080369. doi: 10.3389/fmicb.2023.1080369. eCollection 2023.
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Epigenetics in Tuberculosis: Immunomodulation of Host Immune Response.结核病中的表观遗传学:宿主免疫反应的免疫调节
Vaccines (Basel). 2022 Oct 18;10(10):1740. doi: 10.3390/vaccines10101740.
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MicroRNAs as diagnostic biomarkers for Tuberculosis: A systematic review and meta- analysis.微小 RNA 作为结核病的诊断生物标志物:系统评价和荟萃分析。
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