Allergy and Clinical Immunology Branch, Health Effects Laboratory Division, National Institute for Occupational Safety and Health, Centers for Disease Control and Prevention, Morgantown, WV, United States.
Health Effects Laboratory Division, National Institute for Occupational Safety and Health, Centers for Disease Control and Prevention, Morgantown, WV, United States.
Front Immunol. 2018 Feb 7;9:170. doi: 10.3389/fimmu.2018.00170. eCollection 2018.
Fungal bioaerosols are ubiquitous in the environment and human exposure can result in a variety of health effects ranging from systemic, subcutaneous, and cutaneous infections to respiratory morbidity including allergy, asthma, and hypersensitivity pneumonitis. Recent research has focused on the role of microRNAs (miRNAs) following fungal exposure and is overlooked, yet important, group of regulators capable of influencing fungal immune responses through a variety of cellular mechanisms. These small non-coding ribose nucleic acids function to regulate gene expression at the post-transcriptional level and have been shown to participate in multiple disease pathways including cancer, heart disease, apoptosis, as well as immune responses to microbial hazards and occupational allergens. Recent animal model studies have characterized miRNAs following the exposure to inflammatory stimuli. Studies focused on microbial exposure, including bacterial infections, as well as exposure to different allergens have shown miRNAs, such as miR-21, miR-146, miR-132, miR-155, and the let-7 family members, to be involved in immune and inflammatory responses. Interestingly, the few studies have assessed that the miRNA profiles following fungal exposure have identified the same critical miRNAs that have been characterized in other inflammatory-mediated and allergy-induced experimental models. Review of available , animal and human studies of exposures to , and identified several miRNAs that were shared between responses to these species including miR-125 a/b (macrophage polarization/activation), miR-132 [toll-like receptor (TLR)2-mediated signaling], miR-146a (TLR mediated signaling, alternative macrophage activation), and miR-29a/b (natural killer cell function, C-leptin signaling, inhibition of Th1 immune response). Although these datasets provide preliminary insight into the role of miRNAs in fungal exposed models, interpretation of miRNA datasets can be challenging for researchers. To assist in navigating this rapidly evolving field, the aim of this review is to describe miRNAs in the framework of host recognition mechanisms and provide initial insight into the regulatory pathways in response to fungal exposure.
真菌生物气溶胶在环境中无处不在,人类暴露于真菌生物气溶胶中会导致多种健康影响,包括系统性、皮下和皮肤感染,以及呼吸道疾病,包括过敏、哮喘和过敏性肺炎。最近的研究集中在真菌暴露后 microRNAs(miRNAs)的作用上,而 microRNAs 是一类能够通过多种细胞机制影响真菌免疫反应的重要调控因子。这些小的非编码核糖核酸通过在转录后水平调节基因表达来发挥作用,并且已经参与到多种疾病途径中,包括癌症、心脏病、细胞凋亡,以及对微生物危害和职业过敏原的免疫反应。最近的动物模型研究已经对暴露于炎症刺激后的 microRNAs 进行了特征描述。研究集中在微生物暴露,包括细菌感染,以及暴露于不同过敏原后,表明 miRNAs,如 miR-21、miR-146、miR-132、miR-155 和 let-7 家族成员,参与免疫和炎症反应。有趣的是,少数研究评估了真菌暴露后 miRNA 谱,发现了与其他炎症介导和过敏诱导实验模型中特征化的相同关键 miRNAs。对现有关于接触真菌、细菌和真菌暴露的动物和人类研究的综述,确定了几种在这些物种的反应中共享的 miRNAs,包括 miR-125a/b(巨噬细胞极化/激活)、miR-132[TLR( toll-like receptor)2 介导的信号转导]、miR-146a(TLR 介导的信号转导,替代巨噬细胞激活)和 miR-29a/b(自然杀伤细胞功能、C-瘦素信号转导、抑制 Th1 免疫反应)。尽管这些数据集为 miRNAs 在真菌暴露模型中的作用提供了初步的见解,但 miRNA 数据集的解释对研究人员来说可能具有挑战性。为了帮助研究人员了解这一快速发展的领域,本综述的目的是描述 miRNAs 在宿主识别机制中的作用,并提供对真菌暴露后调控途径的初步了解。