Israr Mohd, Mitchell Danielle, Alam Samina, Dinello Donald, Kishel Joseph J, Meyers Craig
Department of Microbiology and Immunology, Pennsylvania State University College of Medicine, Hershey, PA, USA.
Antivir Ther. 2010;15(2):253-65. doi: 10.3851/IMP1512.
HIV-positive patients taking antiretroviral drugs, including protease inhibitors, have shown a significant increase in the development of oral complications; these complications are a major health issue for affected patients. The effect of these drugs on oral epithelium growth and differentiation is presently unknown. In this study, we explore for the first time the effect of the HIV protease inhibitor amprenavir on gingival epithelium growth and differentiation.
Organotypic (raft) cultures of gingival keratinocytes were established and the raft cultures treated with a range of amprenavir concentrations. Haematoxylin and eosin staining was performed to examine the effect of amprenavir on gingival epithelium growth and stratification. The raft cultures were also immunohistochemically analysed to determine the effect of amprenavir on the expression of key differentiation and proliferation markers, including cytokeratins, proliferating cell nuclear antigen (PCNA) and cyclin A.
Amprenavir severely inhibited the growth of gingival epithelium when the drug was present throughout the growth period of the tissue. When the drug was added at day 8, amprenavir treatment altered the proliferation and differentiation of gingival keratinocytes. Expression of the cytokeratins 5, 14, 6 and 10, PCNA and cyclin A was increased; their expression pattern was also altered over time in treated rafts. Biochemically, the tissue exhibited characteristics of increased proliferation in the suprabasal layers of amprenavir-treated tissue.
Our results suggest that amprenavir treatment deregulates the cell cycle/proliferation and differentiation pathways, resulting in abnormal epithelial repair and proliferation. Our system could be developed as a potential model for studying the effects of highly active antiretroviral therapy in vitro.
服用抗逆转录病毒药物(包括蛋白酶抑制剂)的HIV阳性患者出现口腔并发症的情况显著增加;这些并发症是受影响患者的一个主要健康问题。目前尚不清楚这些药物对口腔上皮生长和分化的影响。在本研究中,我们首次探究了HIV蛋白酶抑制剂安普那韦对牙龈上皮生长和分化的影响。
建立牙龈角质形成细胞的器官型(筏式)培养物,并用一系列安普那韦浓度处理筏式培养物。进行苏木精和伊红染色以检查安普那韦对牙龈上皮生长和分层的影响。还对筏式培养物进行免疫组织化学分析,以确定安普那韦对关键分化和增殖标志物(包括细胞角蛋白、增殖细胞核抗原(PCNA)和细胞周期蛋白A)表达的影响。
当在组织的整个生长期间存在该药物时,安普那韦严重抑制牙龈上皮的生长。当在第8天添加该药物时,安普那韦处理改变了牙龈角质形成细胞的增殖和分化。细胞角蛋白5、14、6和10、PCNA和细胞周期蛋白A的表达增加;在处理过的筏式培养物中,它们的表达模式也随时间发生了改变。从生化角度来看,该组织在安普那韦处理的组织的基底层以上各层表现出增殖增加的特征。
我们的结果表明,安普那韦处理会使细胞周期/增殖和分化途径失调,导致上皮修复和增殖异常。我们的系统可被开发为在体外研究高效抗逆转录病毒疗法效果的潜在模型。