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球孢子菌属感染对中枢神经系统细胞连接复合体的影响。

The Impact of Paracoccidioides spp Infection on Central Nervous System Cell Junctional Complexes.

机构信息

Medical Pathology Department, School of Medicine, Universidade Federal do Paraná, Curitiba, Paraná, Brazil.

Neuroinfection Outclinic, Hospital de Clinicas, Universidade Federal do Paraná, Rua Padre Camargo 280, Curitiba, Paraná, 80060-240, Brazil.

出版信息

Mycopathologia. 2022 Dec;187(5-6):567-577. doi: 10.1007/s11046-022-00653-6. Epub 2022 Aug 3.

Abstract

Paracoccidioidomycosis (PCM), a systemic mycosis caused by the fungus Paracoccidioides spp. is the most prevalent fungal infection among immunocompetent patients in Latin America. The estimated frequency of central nervous system (CNS) involvement among the human immunodeficiency virus (HIV)/PCM-positive population is 2.5%. We aimed to address the impact of neuroparacoccidioidomycosis (NPCM) and HIV/NPCM co-infection on the tight junctions (TJ) and adherens junction (AJ) proteins of the CNS. Four CNS formalin-fixed paraffin-embedded (FFPE) tissue specimens were studied: NPCM, NPCM/HIV co-infection, HIV-positive without opportunistic CNS infection, and normal brain autopsy (negative control). Immunohistochemistry was used to analyze the endothelial cells and astrocytes expressions of TJ markers: claudins (CLDN)-1, -3, -5 and occludin; AJ markers: β-catenin and E-cadherin; and pericyte marker: alpha-smooth muscle actin. FFPE CNS tissue specimens were analyzed using the immunoperoxidase assay. CLDN-5 expression in the capillaries of the HIV/NPCM coinfected tissues (mixed clinical form of PCM) was lower than that in the capillaries of the HIV or NPCM monoinfected (chronic clinical form of PCM) tissues. A marked decrease in CLDN-5 expression and a compensatory increase in CLDN-1 expression in the NPCM/HIV co-infection tissue samples was observed. The authors suggest that Paracoccidioides spp. crosses the blood-brain barrier through paracellular pathway, owing to the alteration in the CLDN expression, or inside the macrophages (Trojan horse).

摘要

副球孢子菌病(PCM)是一种由副球孢子菌属真菌引起的系统性真菌病,是拉丁美洲免疫功能正常患者中最常见的真菌感染。人类免疫缺陷病毒(HIV)/PCM 阳性人群中中枢神经系统(CNS)受累的估计频率为 2.5%。我们旨在探讨神经副球孢子菌病(NPCM)和 HIV/NPCM 合并感染对 CNS 紧密连接(TJ)和黏附连接(AJ)蛋白的影响。研究了 4 个 CNS 福尔马林固定石蜡包埋(FFPE)组织标本:NPCM、NPCM/HIV 合并感染、HIV 阳性但无机会性 CNS 感染和正常脑尸检(阴性对照)。免疫组织化学用于分析 TJ 标志物:紧密连接蛋白(CLDN)-1、-3、-5 和闭锁蛋白;AJ 标志物:β-连环蛋白和 E-钙黏蛋白;和周细胞标志物:α-平滑肌肌动蛋白在血管内皮细胞和星形胶质细胞中的表达。使用免疫过氧化物酶检测法分析 FFPE CNS 组织标本。HIV/NPCM 合并感染组织(PCM 混合临床形式)中毛细血管的 CLDN-5 表达低于 HIV 或 NPCM 单一感染(PCM 慢性临床形式)组织中的毛细血管。在 NPCM/HIV 合并感染组织样本中观察到 CLDN-5 表达明显下降和 CLDN-1 表达代偿性增加。作者认为,副球孢子菌属通过 CLDN 表达的改变,或通过巨噬细胞(特洛伊木马),通过细胞旁途径穿过血脑屏障。

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