Calvet Cláudia M, Oliveira Francisco O R, Araújo-Jorge Tânia C, Pereira Mirian C S
Laboratório de Ultra-estrutura Celular, Instituto Oswaldo Cruz/FIOCRUZ, Av. Brasil 4365, Manguinhos, 21045-900 Rio de Janeiro, RJ, Brazil.
Int J Med Microbiol. 2009 Apr;299(4):301-12. doi: 10.1016/j.ijmm.2008.08.005. Epub 2008 Oct 16.
Alterations in the extracellular matrix have been observed in the cardiomyopathy of Chagas disease caused by Trypanosoma cruzi infection. However, the mechanism of extracellular matrix regulation in T. cruzi-infected cultured cardiomyocytes (CMs) is unclear. Using confocal laser microscopy, we demonstrated that treatment of these cultures with transforming growth factor beta (TGF-beta) and tumor necrosis factor alpha (TNF-alpha) leads to an enhancement of the fibronectin matrix only in uninfected CMs, while infected myocytes displayed low fibronectin expression. Digital image analysis also revealed low superposition of the fibronectin signal with parasite nests in cytokine treated and untreated cultures. Cytochalasin D treatment resulted in microfilament disarray that induced a disturbance in the fibronectin network of CMs, suggesting that cytoskeleton disruption caused by T. cruzi infection disorganizes the fibronectin matrix. Western blot analysis revealed a 2-fold increase in the fibronectin expression in CM cultures after cytokine treatment, whereas T. cruzi infection significantly reduced fibronectin levels in all conditions. In contrast, no change in the laminin expression was detected after cytokine treatment. Laminin distribution was altered in T. cruzi-infected CMs, with intense laminin labeling only at the cell periphery even after cytokine treatment. Our observations indicate that TGF-beta and TNF-alpha stimulates fibronectin expression only in uninfected cells of the T. cruzi-infected cultures, whereas the cells harboring the parasites display low or no fibronectin fibrils.
在由克氏锥虫感染引起的恰加斯病心肌病中,已观察到细胞外基质的改变。然而,克氏锥虫感染的培养心肌细胞(CMs)中细胞外基质调节的机制尚不清楚。使用共聚焦激光显微镜,我们证明用转化生长因子β(TGF-β)和肿瘤坏死因子α(TNF-α)处理这些培养物仅在未感染的CMs中导致纤连蛋白基质增强,而感染的心肌细胞显示出低纤连蛋白表达。数字图像分析还显示在细胞因子处理和未处理的培养物中,纤连蛋白信号与寄生虫巢的叠加程度较低。细胞松弛素D处理导致微丝紊乱,进而引起CMs纤连蛋白网络的紊乱,这表明克氏锥虫感染引起的细胞骨架破坏使纤连蛋白基质紊乱。蛋白质印迹分析显示细胞因子处理后CM培养物中纤连蛋白表达增加了2倍,而在所有条件下克氏锥虫感染均显著降低了纤连蛋白水平。相比之下,细胞因子处理后未检测到层粘连蛋白表达的变化。在克氏锥虫感染的CMs中,层粘连蛋白分布发生改变,即使在细胞因子处理后,仅在细胞周边有强烈的层粘连蛋白标记。我们的观察结果表明,TGF-β和TNF-α仅在克氏锥虫感染培养物的未感染细胞中刺激纤连蛋白表达,而携带寄生虫的细胞显示低纤连蛋白原纤维或无纤连蛋白原纤维。