Department of Cell Biology, Charles University, Viničná 7, Prague, Czech Republic.
Biotechnology and Biomedicine Centre of the Academy of Sciences and Charles University (BIOCEV), Průmyslová 595, 25242, Vestec u Prahy, Czech Republic.
Sci Data. 2018 Oct 2;5:180198. doi: 10.1038/sdata.2018.198.
M2-polarized macrophages have been shown to adapt their 3D migration mode to physical properties of surrounding extracellular matrix. They migrate in the integrin-mediated adhesion and proteolytic activity-dependent "mesenchymal" mode in stiff matrices and in the integrin and protease-independent "amoeboid" mode in low density, porous environments. To find out what impact the switching between the migration modes has on expression of both protein-coding and non-coding genes we employed RNA sequencing of total RNA depleted of ribosomal RNA isolated from macrophages migrating in either mode in 3D collagens. Differentially expressed genes from both categories have been detected and the changes in expression of selected genes were further validated with RT-qPCR. The acquired data will facilitate better understanding of how mechanical properties of tissue microenvironment reflect in macrophage immune function and how the transitions between mesenchymal and amoeboid migratory modes are regulated at the gene expression level.
M2 极化的巨噬细胞已经被证明能够根据周围细胞外基质的物理特性来调整其 3D 迁移模式。在刚性基质中,它们以整合素介导的黏附和蛋白水解活性依赖性的“间质”模式迁移,而在低密度多孔环境中,它们以整合素和蛋白酶非依赖性的“阿米巴样”模式迁移。为了了解迁移模式之间的转换对蛋白质编码基因和非编码基因表达的影响,我们采用了 RNA 测序技术,对在 3D 胶原中以两种模式迁移的巨噬细胞中分离的核糖体 RNA 去除后的总 RNA 进行了测序。从这两个类别中检测到了差异表达的基因,并通过 RT-qPCR 进一步验证了选定基因表达的变化。所获得的数据将有助于更好地理解组织微环境的机械特性如何反映在巨噬细胞免疫功能中,以及在基因表达水平上如何调节间质样和阿米巴样迁移模式之间的转变。