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miRNome 表达分析揭示麻风免疫病理生理学的新参与者。

miRNome Expression Analysis Reveals New Players on Leprosy Immune Physiopathology.

机构信息

Laboratório de Dermato-Imunologia, Instituto de Ciências Biológicas (ICB), Universidade Federal do Pará (UFPA), Marituba, Brazil.

Laboratório de Genética Humana e Médica, ICB, UFPA, Belém, Brazil.

出版信息

Front Immunol. 2018 Mar 9;9:463. doi: 10.3389/fimmu.2018.00463. eCollection 2018.

Abstract

Leprosy remains as a public health problem and its physiopathology is still not fully understood. MicroRNAs (miRNA) are small RNA non-coding that can interfere with mRNA to regulate gene expression. A few studies using DNA chip microarrays have explored the expression of miRNA in leprosy patients using a predetermined set of genes as targets, providing interesting findings regarding the regulation of immune genes. However, using a predetermined set of genes restricted the possibility of finding new miRNAs that might be involved in different mechanisms of disease. Thus, we examined the miRNome of tuberculoid (TT) and lepromatous (LL) patients using both blood and lesional biopsies from classical leprosy patients (LP) who visited the Dr. Marcello Candia Reference Unit in Sanitary Dermatology in the State of Pará and compared them with healthy subjects. Using a set of tools to correlate significantly differentially expressed miRNAs with their gene targets, we identified possible interactions and networks of miRNAs that might be involved in leprosy immunophysiopathology. Using this approach, we showed that the leprosy miRNA profile in blood is distinct from that in lesional skin as well as that four main groups of genes are the targets of leprosy miRNA: (1) recognition and phagocytosis, with activation of immune effector cells, where the immunosuppressant profile of LL and immunoresponsive profile of TT are clearly affected by miRNA expression; (2) apoptosis, with supportive data for an antiapoptotic leprosy profile based on , and expression; (3) Schwann cells (SCs), demyelination and epithelial-mesenchymal transition (EMT), supporting a role for different developmental or differentiation gene families, such as Sox, Zeb, and Hox; and (4) loss of sensation and neuropathic pain, revealing that , and aquaporin-1 () may be involved in the loss of sensation or leprosy pain, indicating possible new therapeutic targets. Additionally, may also be involved in skin dryness and loss of elasticity, which are well known signs of leprosy but with unrecognized physiopathology. In sum, miRNA expression reveals new aspects of leprosy immunophysiopathology, especially on the regulation of the immune system, apoptosis, SC demyelination, EMT, and neuropathic pain.

摘要

麻风仍然是一个公共卫生问题,其病理生理学仍未完全被理解。微小 RNA(miRNA)是一种非编码的小 RNA,可以干扰 mRNA 来调节基因表达。一些使用 DNA 芯片微阵列的研究已经使用预定的基因集作为靶点探索了麻风病患者中 miRNA 的表达,这些研究提供了有关免疫基因调控的有趣发现。然而,使用预定的基因集限制了发现可能涉及疾病不同机制的新 miRNA 的可能性。因此,我们使用来自巴西马拉尼昂州 Sanitary Dermatology 州立 Dr. Marcello Candia 参考单位就诊的经典麻风病患者的血液和病变活检检查了结核样型(TT)和瘤型(LL)患者的 miRNome,并将其与健康受试者进行了比较。使用一组工具将差异表达 miRNA 与其基因靶点相关联,我们鉴定了可能参与麻风病免疫病理生理学的 miRNA 相互作用和网络。使用这种方法,我们表明血液中的麻风 miRNA 谱与皮肤病变中的 miRNA 谱不同,并且有四个主要的基因群是麻风 miRNA 的靶点:(1)识别和吞噬作用,伴有免疫效应细胞的激活,其中 LL 的免疫抑制和 TT 的免疫反应性受 miRNA 表达的明显影响;(2)细胞凋亡,有支持麻风细胞凋亡谱的证据,基于 和 的表达;(3)许旺细胞(SCs)、脱髓鞘和上皮间质转化(EMT),支持不同发育或分化基因家族的作用,如 Sox、Zeb 和 Hox;(4)感觉丧失和神经病理性疼痛,表明 和水通道蛋白-1(AQP1)可能与感觉丧失或麻风病疼痛有关,提示可能有新的治疗靶点。此外,miR-196a 也可能参与皮肤干燥和失去弹性,这是麻风病的已知特征,但病理生理学尚未被认识。总之,miRNA 表达揭示了麻风病免疫病理生理学的新方面,特别是对免疫系统、细胞凋亡、SCs 脱髓鞘、EMT 和神经病理性疼痛的调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e3b/5854644/dc66340fa405/fimmu-09-00463-g001.jpg

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