D'Angelo William, Acharya Dhiraj, Wang Ruoxing, Wang Jundi, Gurung Chandan, Chen Bohan, Bai Fengwei, Guo Yan-Lin
1 Department of Biological Sciences, the University of Southern Mississippi , Hattiesburg, Mississippi.
2 Department of Cancer Biology, University of Pennsylvania School of Medicine , Philadelphia, Pennsylvania.
Stem Cells Dev. 2016 Apr 15;25(8):648-59. doi: 10.1089/scd.2015.0377. Epub 2016 Mar 17.
The innate immunity of embryonic stem cells (ESCs) has recently emerged as an important issue in ESC biology and in ESC-based regenerative medicine. We have recently reported that mouse ESCs (mESCs) do not have a functional type I interferon (IFN)-based antiviral innate immunity. They are deficient in expressing IFN in response to viral infection and have limited ability to respond to IFN. Using fibroblasts (FBs) as a cell model, the current study investigated the development of antiviral mechanisms during in vitro differentiation of mESCs. We demonstrate that mESC-differentiated FBs (mESC-FBs) share extensive similarities with naturally differentiated FBs in morphology, marker expression, and growth pattern, but their development of antiviral mechanisms lags behind. Nonetheless, the antiviral mechanisms are inducible during mESC differentiation as demonstrated by the transition of nuclear factor kappa B (NFκB), a key transcription factor for IFN expression, from its inactive state in mESCs to its active state in mESC-FBs and by increased responses of mESC-FBs to viral stimuli and IFN during their continued in vitro propagation. Together with our previously published study, the current data provide important insights into molecular basis for the deficiency of IFN expression in mESCs and the development of antiviral innate immunity during mESC differentiation.
胚胎干细胞(ESC)的固有免疫最近已成为ESC生物学和基于ESC的再生医学中的一个重要问题。我们最近报道,小鼠胚胎干细胞(mESC)不具有基于I型干扰素(IFN)的功能性抗病毒固有免疫。它们在病毒感染时表达IFN存在缺陷,并且对IFN的反应能力有限。本研究以成纤维细胞(FB)为细胞模型,调查了mESC体外分化过程中抗病毒机制的发展。我们证明,mESC分化的FB(mESC-FB)在形态、标志物表达和生长模式上与自然分化的FB有广泛的相似性,但它们抗病毒机制的发展滞后。尽管如此,如关键转录因子核因子κB(NFκB)从mESC中的无活性状态转变为mESC-FB中的活性状态,以及mESC-FB在体外持续增殖过程中对病毒刺激和IFN的反应增加所示,抗病毒机制在mESC分化过程中是可诱导的。与我们之前发表的研究一起,当前数据为mESC中IFN表达缺陷的分子基础以及mESC分化过程中抗病毒固有免疫的发展提供了重要见解。