North Carolina State University, College of Veterinary Medicine, 4700 Hillsborough Street, Raleigh, NC 27606, USA.
Parasitol Res. 2010 May;106(6):1507-11. doi: 10.1007/s00436-010-1837-7. Epub 2010 Mar 30.
We hypothesized that unrecognized differences in epithelial expression of inducible nitric oxide synthase (iNOS), resulting from engineered immunodeficiency, could explain the contradictory findings of prior studies regarding the importance of nitric oxide (NO) in murine models of Cryptosporidium parvum infection. Severe combined immunodeficient mice (SCID) failed to constitutively or inducibly express epithelial iNOS or increase NO synthesis in response to C. parvum infection. In contrast, mice lacking IFN-gamma alone induced both epithelial iNOS expression and NO synthesis in response to infection. Accordingly, lymphocytes mediate epithelial expression of iNOS and NO synthesis independent of IFN-gamma in response to C. parvum infection. These findings in large part explain the contradictory conclusions of prior studies regarding the role of iNOS in C. parvum infection.
我们假设,由于基因工程导致的免疫缺陷,诱导型一氧化氮合酶(iNOS)在肠道上皮细胞中的表达存在未被识别的差异,这可能解释了先前关于一氧化氮(NO)在隐孢子虫感染的小鼠模型中重要性的研究结果存在矛盾的原因。严重联合免疫缺陷(SCID)小鼠不能持续或诱导性地表达肠道上皮细胞 iNOS,也不能增加 NO 的合成以响应隐孢子虫感染。相比之下,单独缺乏 IFN-γ的小鼠在感染后诱导肠道上皮细胞 iNOS 的表达和 NO 的合成。因此,淋巴细胞介导肠道上皮细胞 iNOS 的表达和 NO 的合成,这一过程独立于 IFN-γ,响应隐孢子虫感染。这些发现在很大程度上解释了先前关于 iNOS 在隐孢子虫感染中的作用的研究结果存在矛盾的原因。