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克氏锥虫感染可诱导小鼠心肌细胞中CD40的表达,有利于依赖CD40连接产生致心性白细胞介素-6。

Trypanosoma cruzi infection induces the expression of CD40 in murine cardiomyocytes favoring CD40 ligation-dependent production of cardiopathogenic IL-6.

作者信息

Ayala Mariela Alejandra Moreno, Casasco Agustina, González Mariela, Postan Miriam, Corral Ricardo Santiago, Petray Patricia Beatriz

机构信息

Servicio de Parasitología y Enfermedad de Chagas, Hospital de Niños Ricardo Gutiérrez, Gallo 1330, Buenos Aires, Argentina.

Instituto de Investigaciones Biomédicas (UBA-CONICET), Facultad de Medicina, Universidad de Buenos Aires, Paraguay 2155, piso 10, Buenos Aires, Argentina.

出版信息

Parasitol Res. 2016 Feb;115(2):779-85. doi: 10.1007/s00436-015-4805-4. Epub 2015 Nov 3.

Abstract

The inflammatory response in the myocardium is an important aspect of the pathogenesis of Chagas' heart disease raised by Trypanosoma cruzi. CD40, a transmembrane type I receptor belonging to the tumor necrosis factor receptor (TNFR) family, is expressed in a broad spectrum of cell types and is crucial in several inflammatory and autoimmune diseases. Activation of CD40 through ligation to CD40L (CD154) induces multiple effects, including the secretion of proinflammatory molecules. In the present study, we examined the ability of T. cruzi to trigger the expression of CD40 in cardiac myocytes in vitro and in a murine model of chagasic cardiomyopathy. Our results indicate, for the first time, that T. cruzi is able to induce the expression of CD40 in HL-1 murine cardiomyocytes. Moreover, ligation of CD40 receptor upregulated interleukin-6 (IL-6), associated with inflammation. Furthermore, the induction of this costimulatory molecule was demonstrated in vivo in myocardium of mice infected with T. cruzi. This suggests that CD40-bearing cardiac muscle cells could interact with CD40L-expressing lymphocytes infiltrating the heart, thus contributing to inflammatory injury in chagasic cardiomyopathy.

摘要

心肌中的炎症反应是由克氏锥虫引发的恰加斯心脏病发病机制的一个重要方面。CD40是一种属于肿瘤坏死因子受体(TNFR)家族的跨膜I型受体,在多种细胞类型中表达,并且在几种炎症和自身免疫性疾病中起关键作用。通过与CD40配体(CD154)结合激活CD40会诱导多种效应,包括促炎分子的分泌。在本研究中,我们检测了克氏锥虫在体外以及在恰加斯心肌病小鼠模型中触发心肌细胞中CD40表达的能力。我们的结果首次表明,克氏锥虫能够在HL-1小鼠心肌细胞中诱导CD40的表达。此外,CD40受体的结合上调了与炎症相关的白细胞介素-6(IL-6)。此外,在感染克氏锥虫的小鼠心肌中,体内证实了这种共刺激分子的诱导。这表明携带CD40的心肌细胞可能与浸润心脏的表达CD40L的淋巴细胞相互作用,从而导致恰加斯心肌病中的炎症损伤。

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