Swonger Jessica M, Liu Jocelyn S, Ivey Malina J, Tallquist Michelle D
Departments of Medicine and Cell and Molecular Biology, John A. Burns School of Medicine, University of Hawaii, Honolulu, HI 96813, USA.
Departments of Medicine and Cell and Molecular Biology, John A. Burns School of Medicine, University of Hawaii, Honolulu, HI 96813, USA.
Differentiation. 2016 Sep;92(3):66-83. doi: 10.1016/j.diff.2016.05.009. Epub 2016 Jun 21.
The use of mouse genetic tools to track and manipulate fibroblasts has provided invaluable in vivo information regarding the activities of these cells. Recently, many new mouse strains have been described for the specific purpose of studying fibroblast behavior. Colorimetric reporter mice and lines expressing Cre are available for the study of fibroblasts in the organs prone to fibrosis, including heart, kidney, liver, lung, and skeletal muscle. In this review we summarize the current state of the models that have been used to define tissue resident fibroblast populations. While these complex genetic reagents provide unique insights into the process of fibrosis, they also require a thorough understanding of the caveats and limitations. Here, we discuss the specificity and efficiency of the available genetic models and briefly describe how they have been used to document the mechanisms of fibrosis.
利用小鼠遗传工具追踪和操纵成纤维细胞,为了解这些细胞的活动提供了宝贵的体内信息。最近,为了专门研究成纤维细胞的行为,已经描述了许多新的小鼠品系。用于研究易发生纤维化器官(包括心脏、肾脏、肝脏、肺和骨骼肌)中 的成纤维细胞的比色报告基因小鼠和表达Cre的品系均已问世。在本综述中,我们总结了用于定义组织驻留成纤维细胞群体的模型的当前状态。虽然这些复杂的遗传试剂为纤维化过程提供了独特的见解,但它们也需要对注意事项和局限性有透彻的了解。在这里,我们讨论了现有遗传模型的特异性和效率,并简要描述了它们如何被用于记录纤维化的机制。