Lisse Thomas S, Brochu Elizabeth A, Rieger Sandra
Davis Center for Regenerative Biology and Medicine, MDI Biological Laboratory.
Davis Center for Regenerative Biology and Medicine, MDI Biological Laboratory;
J Vis Exp. 2015 Jan 31(95):52654. doi: 10.3791/52654.
The zebrafish larval tail fin is ideal for studying tissue regeneration due to the simple architecture of the larval fin-fold, which comprises of two layers of skin that enclose undifferentiated mesenchyme, and because the larval tail fin regenerates rapidly within 2-3 days. Using this system, we demonstrate a method for capturing the repair dynamics of the amputated tail fin with time-lapse video brightfield stereomicroscopy. We demonstrate that fin amputation triggers a contraction of the amputation wound and extrusion of cells around the wound margin, leading to their subsequent clearance. Fin regeneration proceeds from proximal to distal direction after a short delay. In addition, developmental growth of the larva can be observed during all stages. The presented method provides an opportunity for observing and analyzing whole tissue-scale behaviors such as fin development and growth in a simple microscope setting, which is easily adaptable to any stereomicroscope with time-lapse capabilities.
斑马鱼幼体的尾鳍对于研究组织再生而言是理想的,这是因为幼体鳍褶的结构简单,它由两层皮肤组成,这两层皮肤包围着未分化的间充质,而且幼体尾鳍能在2到3天内迅速再生。利用这个系统,我们展示了一种通过延时视频明场立体显微镜来捕捉截断尾鳍修复动态的方法。我们证明,鳍截断会引发截断伤口的收缩以及伤口边缘细胞的挤出,从而导致这些细胞随后被清除。鳍的再生在短暂延迟后从近端向远端进行。此外,在所有阶段都能观察到幼体的发育生长。所呈现的方法为在简单的显微镜设置下观察和分析诸如鳍发育和生长等全组织尺度的行为提供了机会,这种设置很容易适配任何具有延时功能的立体显微镜。