Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA 94305, USA
Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Development. 2020 Jun 17;147(12):dev183640. doi: 10.1242/dev.183640.
Cell ablation is a powerful method for elucidating the contributions of individual cell populations to embryonic development and tissue regeneration. Targeted cell loss in whole organisms has been typically achieved through expression of a cytotoxic or prodrug-activating gene product in the cell type of interest. This approach depends on the availability of tissue-specific promoters, and it does not allow further spatial selectivity within the promoter-defined region(s). To address this limitation, we have used the light-inducible GAVPO transactivator in combination with two genetically encoded cell-ablation technologies: the nitroreductase/nitrofuran system and a cytotoxic variant of the M2 ion channel. Our studies establish ablative methods that provide the tissue specificity afforded by regulatory elements and the conditionality of optogenetics. Our studies also demonstrate differences between the nitroreductase and M2 systems that influence their efficacies for specific applications. Using this integrative approach, we have ablated cells in zebrafish embryos with both spatial and temporal control.
细胞消融是阐明单个细胞群体对胚胎发育和组织再生贡献的有力方法。在整个生物体中靶向细胞缺失通常通过在感兴趣的细胞类型中表达细胞毒性或前药激活基因产物来实现。这种方法取决于组织特异性启动子的可用性,并且不允许在启动子定义的区域内进一步进行空间选择性。为了解决这个限制,我们使用了光诱导的 GAVPO 转录激活子与两种基因编码的细胞消融技术结合使用:硝基还原酶/硝基呋喃系统和 M2 离子通道的细胞毒性变体。我们的研究建立了消融方法,这些方法提供了调控元件所赋予的组织特异性和光遗传学的条件性。我们的研究还表明,硝基还原酶和 M2 系统之间存在差异,这会影响它们在特定应用中的功效。使用这种综合方法,我们已经在斑马鱼胚胎中进行了具有时空控制的细胞消融。