Department of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Department of Dermatology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
J Cell Sci. 2022 Oct 15;135(20). doi: 10.1242/jcs.260594. Epub 2022 Oct 26.
A large group of keratin genes (n=54 in the human genome) code for intermediate filament (IF)-forming proteins and show differential regulation in epithelial cells and tissues. Keratin expression can be highly informative about the type of epithelial tissue, differentiation status of constituent cells and biological context (e.g. normal versus diseased settings). The foundational principles underlying the use of keratin expression to gain insight about epithelial cells and tissues primarily originated in pioneering studies conducted in the 1980s. The recent emergence of single cell transcriptomics provides an opportunity to revisit these principles and gain new insight into epithelial biology. Re-analysis of single-cell RNAseq data collected from human and mouse skin has confirmed long-held views regarding the quantitative importance and pairwise regulation of specific keratin genes in keratinocytes of surface epithelia. Furthermore, such analyses confirm and extend the notion that changes in keratin gene expression occur gradually as progenitor keratinocytes commit to and undergo differentiation, and challenge the prevailing assumption that specific keratin combinations reflect a mitotic versus a post-mitotic differentiating state. Our findings provide a blueprint for similar analyses in other tissues, and warrant a more nuanced approach in the use of keratin genes as biomarkers in epithelia.
一大组角蛋白基因(人类基因组中共有 54 个)编码中间丝(IF)形成蛋白,并在上皮细胞和组织中表现出差异调节。角蛋白的表达可以提供关于上皮组织类型、组成细胞的分化状态和生物学背景(例如正常与患病状态)的重要信息。利用角蛋白表达来深入了解上皮细胞和组织的基础原理主要源于 20 世纪 80 年代进行的开创性研究。单细胞转录组学的最新出现为重新审视这些原则并深入了解上皮生物学提供了机会。对来自人和小鼠皮肤的单细胞 RNAseq 数据的重新分析证实了长期以来关于表皮角质形成细胞中特定角蛋白基因的定量重要性和成对调节的观点。此外,这些分析证实并扩展了这样一种观点,即角蛋白基因表达的变化是随着祖角质形成细胞的分化而逐渐发生的,并挑战了特定角蛋白组合反映有丝分裂与有丝分裂后分化状态的普遍假设。我们的发现为其他组织中的类似分析提供了蓝图,并需要在使用角蛋白基因作为上皮组织生物标志物时采取更细致的方法。