BIO5 Institute, The University of Arizona, Tucson, AZ, USA.
Department of Immunobiology, BIO5 Institute, The University of Arizona, Tucson, AZ, USA.
Methods Mol Biol. 2021;2244:83-101. doi: 10.1007/978-1-0716-1111-1_5.
Of the many research challenges posed by the study of human cytomegalovirus (HCMV) latency, one of the most notable is the requirement for the use of primary hematopoietic cell culture. Culturing hematopoietic progenitor subpopulations requires that consideration be given to maintaining their physiological relevance. We describe a long-standing primary CD34+ hematopoietic progenitor cell (HPC) system as an in vitro model to study HCMV latent infection. Key aspects of the model include infection of primary human CD34+ HPCs prior to ex vivo expansion, a long-term culture with a stromal cell support designed to maintain the ability of stem cells to support hematopoietic reconstitution, and an assay to quantify infectious centers produced prior to and following a reactivation stimulus. Importantly, this system has been used to identify a number of viral determinants of latency or reactivation and findings have been recapitulated in vivo using a humanized mouse model for HCMV latency. Therefore, this system offers a powerful approach to defining virus-host interactions and mechanisms important for HCMV latency and reactivation.
在研究人类巨细胞病毒 (HCMV) 潜伏性所面临的诸多研究挑战中,其中一个最值得注意的挑战是需要使用原代造血细胞培养。培养造血祖细胞亚群需要考虑保持其生理相关性。我们描述了一种长期存在的原代 CD34+造血祖细胞 (HPC) 系统,作为研究 HCMV 潜伏感染的体外模型。该模型的关键方面包括在体外扩增前感染原代人 CD34+HPC、用基质细胞支持进行长期培养,以维持干细胞支持造血重建的能力,以及一种在重新激活刺激前后定量感染中心的检测方法。重要的是,该系统已被用于鉴定潜伏或重新激活的一些病毒决定因素,并且使用 HCMV 潜伏的人源化小鼠模型在体内重现了这些发现。因此,该系统为定义 HCMV 潜伏和重新激活的病毒-宿主相互作用和机制提供了一种有力的方法。