Miranda Vanessa do Socorro Cabral, Falcão Luiz Fabio Magno, Fuzii Hellen Thais, Carvalho Marcos Luiz Gaia, Lopes Jeferson da Costa, Filho Arnaldo Jorge Martins, Cruz Ana Cecilia Ribeiro, Azevedo Raimunda do Socorro da Silva, Sousa Jorge Rodrigues de, Wakimoto Mayumi Duarte, Vasconcelos Pedro Fernando da Costa, Quaresma Juarez Antônio Simões
Departmento of Pathology, Evandro Chagas Institute, Ministry of Health, Ananindeua 67030-000, PA, Brazil.
Departmento of Pathology, State University of Para, Belem 66050-540, PA, Brazil.
Viruses. 2024 Dec 24;17(1):3. doi: 10.3390/v17010003.
Necroptosis is a regulated form of cell death implicated in several pathological conditions, including viral infections. In this study, we investigated the expression and correlation of necroptosis markers MLKL, RIP1 and RIP3 in human liver tissue from fatal cases of yellow fever (YF) using immunohistochemistry (IHC). The liver samples were obtained from 21 YF-positive individuals and five flavivirus-negative controls with preserved liver parenchymal architecture. The cases underwent histopathological analysis, followed by tissue immunostaining with the immunohistochemical method of streptavidin-biotin peroxidase. Using the in situ method, we evaluated the centrilobular zone (Z3), midzonal zone (Z2), periportal zone and portal tract (PT) of human liver parenchyma with markers for necroptosis, RIPK1, RIPK3 and MLKL. A quantitative analysis revealed a significantly higher expression of MLKL, RIP1 and RIP3 in the liver parenchyma of YF cases compared to controls in different zones (Z3, Z2, Z1) and portal tracts (PTs) of the liver, especially in zone 2. Immunostaining confirmed the localization of MLKL, RIP1 and RIP3 in hepatocytes and inflammatory infiltrates, highlighting their involvement in the pathogenesis of YF. A Pearson correlation analysis demonstrated significant correlations among necroptosis markers, which indicates their coordinated regulation during YF-induced liver injury.
坏死性凋亡是一种受调控的细胞死亡形式,与包括病毒感染在内的多种病理状况有关。在本研究中,我们使用免疫组织化学(IHC)方法,调查了黄热病(YF)致死病例的人肝组织中坏死性凋亡标志物混合谱系激酶结构域样蛋白(MLKL)、受体相互作用蛋白1(RIP1)和受体相互作用蛋白3(RIP3)的表达及相关性。肝样本取自21例YF阳性个体和5例肝实质结构保存完好的黄病毒阴性对照。对这些病例进行了组织病理学分析,随后采用链霉亲和素-生物素过氧化物酶免疫组织化学方法进行组织免疫染色。我们使用原位方法,用坏死性凋亡标志物RIPK1、RIPK3和MLKL评估人肝实质的中央小叶区(Z3)、中间带区(Z2)、门周区和门静脉区(PT)。定量分析显示,与对照组相比,YF病例肝实质不同区域(Z3、Z2、Z1)和肝门静脉区(PTs)中MLKL、RIP1和RIP3的表达显著更高,尤其是在2区。免疫染色证实了MLKL、RIP1和RIP3在肝细胞和炎性浸润中的定位,突出了它们在YF发病机制中的作用。Pearson相关性分析表明坏死性凋亡标志物之间存在显著相关性,这表明它们在YF诱导的肝损伤过程中受到协同调控。