Çevrim Çağrı, Laplace-Builhé Béryl, Sugawara Ko, Rusciano Maria Lorenza, Labert Nicolas, Brocard Jacques, Almazán Alba, Averof Michalis
Institut de Génomique Fonctionnelle de Lyon (IGFL), École Normale Supérieure de Lyon, Lyon, France.
Centre National de la Recherche Scientifique (CNRS), Paris, France.
Elife. 2025 Aug 8;14:RP107534. doi: 10.7554/eLife.107534.
High-resolution live imaging of regeneration presents unique challenges due to the nature of the specimens (large mobile animals), the duration of the process (spanning days or weeks), and the fact that cellular resolution must be achieved without damage caused by lengthy exposures to light. Building on previous work that allowed us to image different parts of the process of leg regeneration in the crustacean , we present here a method for live imaging that captures the entire process of leg regeneration, spanning up to 10 days, at cellular resolution. Our method includes (1) mounting and long-term live imaging of regenerating legs under conditions that yield high spatial and temporal resolution but minimise photodamage, (2) fixing and in situ staining of the regenerated legs that were imaged, to identify cell fates, and (3) computer-assisted cell tracking to determine the cell lineages and progenitors of identified cells. The method is optimised to limit light exposure while maximising tracking efficiency. Combined with appropriate cell-type-specific markers, this method may allow the description of cell lineages for every regenerated cell type in the limb.
由于样本的特性(大型活动动物)、再生过程的持续时间(长达数天或数周),以及必须在不因长时间光照造成损伤的情况下实现细胞分辨率,对再生过程进行高分辨率实时成像面临着独特的挑战。基于之前使我们能够对甲壳类动物腿部再生过程的不同部分进行成像的工作,我们在此提出一种实时成像方法,该方法能够以细胞分辨率捕捉长达10天的腿部再生全过程。我们的方法包括:(1)在能产生高空间和时间分辨率但将光损伤降至最低的条件下,对再生腿部进行固定和长期实时成像;(2)对已成像的再生腿部进行固定和原位染色,以确定细胞命运;(3)通过计算机辅助细胞追踪来确定已识别细胞的细胞谱系和祖细胞。该方法经过优化,以限制光照暴露同时最大化追踪效率。结合适当的细胞类型特异性标记物,此方法可能有助于描述肢体中每种再生细胞类型的细胞谱系。