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精神分裂症患者外周血单核细胞中TLR 1、2和6的分子与功能分析:一项初步研究

Molecular and Functional Analysis of TLR 1, 2 and 6 in Peripheral Blood Monocytes of Patients with Schizophrenia: A Pilot Study.

作者信息

Sotelo-Ramírez Carlo E, Valdés-Tovar Marcela, Zaragoza-Hoyos Julio Uriel, Ortiz-López Leonardo, Argueta Jesús, Rosel-Vales Mauricio, Miranda-Labra Roxana U, Camarena Beatriz

机构信息

Doctorado en Biología Experimental, Universidad Autónoma Metropolitana (UAM)-Iztapalapa, Mexico City 09340, Mexico.

Departamento de Farmacogenética, Subdirección de Investigaciones Clínicas, Instituto Nacional de Psiquiatría Ramón de la Fuente Muñiz, Mexico City 14370, Mexico.

出版信息

Int J Mol Sci. 2025 Jan 23;26(3):926. doi: 10.3390/ijms26030926.

Abstract

Schizophrenia (SZ) is a chronic disabling mental disorder with high heritability, and several immune-regulating genes have been implicated in its pathophysiology In this study, we investigated the expression of Toll-like receptors (TLRs) 1, 2, and 6 in peripheral blood monocytes from SZ patients and healthy control subjects (HCSs) in the Mexican population, focusing on specific SZ-associated gene variants. Gene expressions were assessed by qPCR, and protein expression was measured using flow cytometry. The secretory profiles of MALP2-stimulated monocytes were evaluated through immunoproteomic arrays. Our results indicate that patients with SZ carrying the rs4833093/ GG genotype exhibited significantly lower gene expression compared to TT carriers. Notably, HCSs with the TT genotype showed markedly higher protein expression, while all patients with SZ exhibited significantly reduced protein levels regardless of genotype. Furthermore, monocytes from patients with SZ displayed altered secretion profiles upon TLR stimulation, with significant elevations in IL-18, uPAR, angiopoietin-2, and serpin E1, alongside reductions in MCP-1, IL-17A, IL-24, MIF, and myeloperoxidase compared to HCSs. These findings suggest a dysfunctional TLR-mediated innate immune response in SZ.

摘要

精神分裂症(SZ)是一种具有高遗传性的慢性致残性精神障碍,并且一些免疫调节基因已被认为与它的病理生理学有关。在本研究中,我们调查了墨西哥人群中SZ患者和健康对照者(HCSs)外周血单核细胞中Toll样受体(TLRs)1、2和6的表达,重点关注特定的与SZ相关的基因变体。通过qPCR评估基因表达,并使用流式细胞术测量蛋白质表达。通过免疫蛋白质组阵列评估MALP2刺激的单核细胞的分泌谱。我们的结果表明,携带rs4833093/GG基因型的SZ患者与携带TT基因型的患者相比,基因表达显著降低。值得注意的是,具有TT基因型的HCSs显示出明显更高的蛋白质表达,而所有SZ患者无论基因型如何,蛋白质水平均显著降低。此外,与HCSs相比,SZ患者的单核细胞在TLR刺激后分泌谱发生改变,IL-18、uPAR、血管生成素-2和丝氨酸蛋白酶抑制剂E1显著升高,同时MCP-1、IL-17A、IL-24、MIF和髓过氧化物酶降低。这些发现表明SZ中存在功能失调的TLR介导的先天性免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f32a/11817014/3922f6d29263/ijms-26-00926-g001.jpg

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