Silva Julhiany de Fátima da, Vicentim Juliana, Oliveira Haroldo Cesar de, Marcos Caroline Maria, Assato Patricia Akemi, Andreotti Patrícia Ferrari, Silva Juliana Leal Monteiro da, Soares Christiane Pienna, Benard Gil, Almeida Ana Marisa Fusco, Mendes-Giannini Maria José Soares
Departamento de Análises Clínicas, Faculdade de Ciências Farmacêuticas de Araraquara, Universidade Estadual Paulista, Araraquara, SP, Brasil.
Laboratório de Alergia e Imunologia Clínica e Experimental, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brasil.
Mem Inst Oswaldo Cruz. 2015 Jun;110(4):476-84. doi: 10.1590/0074-02760150057. Epub 2015 Jun 2.
The fungal strain Paracoccidioides brasiliensis remains viable inside of epithelial cells and can induce apoptosis in this population. However, until now, the molecules that participate in this process remained unknown. Thus, this study evaluated the contribution of two P. brasiliensis molecules, the 14-3-3 and glycoprotein of 43 kDa proteins, which had been previously described as extracellular matrix adhesins and apoptosis inductors in human pneumocytes. Accordingly, epithelial cells were treated with these molecules for different periods of time and the expression of the apoptosis regulating-proteins Bak, Bax, Bcl-2, p53 and caspases were evaluated by terminal deoxynucleotidyl transferase dUTP nick end labelling, flow cytometry and real-time polymerase chain reaction analysis. Our results demonstrated that treatment with these molecules induces apoptosis signalling in pulmonary epithelial cells, showing the same pattern of programmed cell-death as that observed during infection with P. brasiliensis. Thus, we could conclude that P. brasiliensis uses these molecules as virulence factors that participate not only in the fungal adhesion process to host cells, but also in other important cellular mechanisms such as apoptosis.
巴西副球孢子菌菌株在上皮细胞内仍具活力,并可在此群体中诱导细胞凋亡。然而,迄今为止,参与这一过程的分子仍不为人知。因此,本研究评估了两种巴西副球孢子菌分子,即14-3-3和43 kDa糖蛋白的作用,这两种分子先前被描述为细胞外基质粘附素和人类肺细胞中的凋亡诱导剂。相应地,用这些分子处理上皮细胞不同时间段,通过末端脱氧核苷酸转移酶dUTP缺口末端标记、流式细胞术和实时聚合酶链反应分析评估凋亡调节蛋白Bak、Bax、Bcl-2、p53和半胱天冬酶的表达。我们的结果表明,用这些分子处理可诱导肺上皮细胞中的凋亡信号,显示出与巴西副球孢子菌感染期间观察到的相同的程序性细胞死亡模式。因此,我们可以得出结论,巴西副球孢子菌将这些分子用作毒力因子,这些因子不仅参与真菌与宿主细胞的粘附过程,还参与其他重要的细胞机制,如细胞凋亡。