National Laboratory of Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.
Nat Protoc. 2012 Dec;7(12):2090-102. doi: 10.1038/nprot.2012.128. Epub 2012 Nov 8.
Postembryonic development is an important process of organismal maturation after embryonic growth. Despite key progress in recent years in understanding embryonic development via fluorescence time-lapse microscopy, comparatively less live-cell imaging of postembryonic development has been done. Here we describe a protocol to image larval development in the nematode Caenorhabditis elegans. Our protocol describes the construction of fluorescent transgenic C. elegans, immobilization of worm larvae and time-lapse microscopy analysis. To improve the throughput of imaging, we developed a C. elegans triple-fluorescence imaging approach with a worm-optimized blue fluorescent protein (TagBFP), green fluorescent protein (GFP) and mCherry. This protocol has been previously applied to time-lapse imaging analysis of Q neuroblast asymmetric division, migration and apoptosis, and we show here that it can also be used to image neuritogenesis in the L1 larvae. Other applications are also possible. The protocol can be completed within 3 h and may provide insights into understanding postembryonic development.
胚胎后发育是生物体在胚胎生长后成熟的一个重要过程。尽管近年来通过荧光延时显微镜在理解胚胎发育方面取得了重要进展,但相对而言,对胚胎后发育的活细胞成像研究较少。本文描述了一种在秀丽隐杆线虫中对幼虫发育进行成像的方法。我们的方案描述了荧光转基因秀丽隐杆线虫的构建、线虫幼虫的固定和延时显微镜分析。为了提高成像通量,我们开发了一种秀丽隐杆线虫三荧光成像方法,使用了一种经过优化的线虫蓝色荧光蛋白(TagBFP)、绿色荧光蛋白(GFP)和 mCherry。该方案以前曾应用于 Q 神经母细胞不对称分裂、迁移和凋亡的延时成像分析,我们在这里还表明,它也可以用于 L1 幼虫的神经突发生成像。其他应用也是可能的。该方案可以在 3 小时内完成,可能有助于理解胚胎后发育。