Moredun Research Institute, Pentlands Science Park, Bush Loan, Penicuik, Midlothian EH26 OPZ, United Kingdom.
J Virol. 2011 Apr;85(7):3341-55. doi: 10.1128/JVI.02481-10. Epub 2011 Jan 26.
Ovine pulmonary adenocarcinoma (OPA) is a transmissible lung cancer of sheep caused by Jaagsiekte sheep retrovirus (JSRV). The details of early events in the pathogenesis of OPA are not fully understood. For example, the identity of the JSRV target cell in the lung has not yet been determined. Mature OPA tumors express surfactant protein-C (SP-C) or Clara cell-specific protein (CCSP), which are specific markers of type II pneumocytes or Clara cells, respectively. However, it is unclear whether these are the cell types initially infected and transformed by JSRV or whether the virus targets stem cells in the lung that subsequently acquire a differentiated phenotype during tumor growth. To examine this question, JSRV-infected lung tissue from experimentally infected lambs was studied at early time points after infection. Single JSRV-infected cells were detectable 10 days postinfection in bronchiolar and alveolar regions. These infected cells were labeled with anti-SP-C or anti-CCSP antibodies, indicating that differentiated epithelial cells are early targets for JSRV infection in the ovine lung. In addition, undifferentiated cells that expressed neither SP-C nor CCSP were also found to express the JSRV Env protein. These results enhance the understanding of OPA pathogenesis and may have comparative relevance to human lung cancer, for which samples representing early stages of tumor growth are difficult to obtain.
绵羊肺腺癌(OPA)是一种由绵羊肺腺瘤病毒(JSRV)引起的传染性绵羊肺癌。OPA 发病机制的早期事件的细节尚不完全清楚。例如,肺部中 JSRV 靶细胞的身份尚未确定。成熟的 OPA 肿瘤表达表面活性剂蛋白-C(SP-C)或克拉拉细胞特异性蛋白(CCSP),分别是 II 型肺泡细胞或克拉拉细胞的特异性标志物。然而,尚不清楚这些是否是最初被 JSRV 感染和转化的细胞类型,或者病毒是否靶向肺中的干细胞,这些干细胞在肿瘤生长过程中随后获得分化表型。为了研究这个问题,研究了实验感染羔羊感染后早期的 JSRV 感染肺组织。在感染后 10 天,可在细支气管和肺泡区域检测到单个 JSRV 感染细胞。这些感染细胞被抗 SP-C 或抗 CCSP 抗体标记,表明分化的上皮细胞是绵羊肺中 JSRV 感染的早期靶标。此外,既不表达 SP-C 也不表达 CCSP 的未分化细胞也被发现表达 JSRV Env 蛋白。这些结果增强了对 OPA 发病机制的理解,并且可能与人类肺癌具有比较相关性,因为很难获得代表肿瘤生长早期阶段的人类肺癌样本。