Glass Christopher K
From the Department of Cellular and Molecular Medicine, University of California, San Diego.
Arterioscler Thromb Vasc Biol. 2015 Apr;35(4):755-62. doi: 10.1161/ATVBAHA.114.304051. Epub 2015 Mar 5.
A major goal of our laboratory is to understand the molecular mechanisms that underlie the development and functions of diverse macrophage phenotypes in health and disease. Recent studies using genetic and genomic approaches suggest a relatively simple model of collaborative and hierarchical interactions between lineage-determining and signal-dependent transcription factors that enable selection and activation of transcriptional enhancers that specify macrophage identity and function. In addition, we have found that it is possible to use natural genetic variation as a powerful tool for advancing our understanding of how the macrophage deciphers the information encoded by the genome to attain specific phenotypes in a context-dependent manner. Here, I will describe our recent efforts to extend genetic and genomic approaches to investigate the roles of distinct tissue environments in determining the phenotypes of different resident populations of macrophages.
我们实验室的一个主要目标是了解在健康和疾病状态下,多种巨噬细胞表型的发育和功能所基于的分子机制。最近使用遗传和基因组方法的研究提出了一个相对简单的模型,即谱系决定转录因子和信号依赖转录因子之间的协作和层级相互作用,这种相互作用能够选择和激活指定巨噬细胞身份和功能的转录增强子。此外,我们发现可以利用自然遗传变异作为一种强大的工具,来加深我们对巨噬细胞如何解读基因组编码信息以在依赖于环境的方式下获得特定表型的理解。在这里,我将描述我们最近为扩展遗传和基因组方法所做的努力,以研究不同组织环境在决定不同驻留巨噬细胞群体表型中的作用。