Sánchez-Gómez Helena, Garrido-Maraver Juan, Rojas-Ríos Patricia
Centro Andaluz de Biología del Desarrollo, CSIC/Universidad Pablo de Olavide/JA.
Centro Andaluz de Biología del Desarrollo, CSIC/Universidad Pablo de Olavide/JA;
J Vis Exp. 2024 Dec 20(214). doi: 10.3791/67389.
Live imaging methods allow the analysis of dynamic cellular processes in detail and in real-time. The Drosophila ovary represents an excellent model to explore the dynamics of a myriad of developmental processes, such as cell division, stemness, differentiation, migration, apoptosis, autophagy, cellular adhesion, etc., over time. Recently, we have implemented an extended ex vivo culture and live imaging of the female Drosophila GSC niche. Using a Drosophila line harboring a GFP::Par-1 transgene as an example, this method allows the visualization of the GSCs' asymmetric division within their niche and the description of the changes in the spectrosome morphology along the cell cycle. Here, we present a detailed protocol for the ex vivo culture of Drosophila germaria, enabling prolonged visualization of the female GSC niche. Importantly, this protocol is broadly applicable to live imaging GSCs with multiple fluorescently tagged proteins of interest that are available in stock centers and/or in the Drosophila research community.
活体成像方法能够详细且实时地分析动态细胞过程。果蝇卵巢是探索众多发育过程(如细胞分裂、干性、分化、迁移、凋亡、自噬、细胞黏附等)随时间变化的动态过程的绝佳模型。最近,我们实现了对雌性果蝇生殖干细胞微环境的扩展离体培养和活体成像。以携带GFP::Par-1转基因的果蝇品系为例,该方法能够可视化生殖干细胞在其微环境中的不对称分裂,并描述沿细胞周期的纺锤体形态变化。在此,我们展示了一份用于果蝇生殖腺离体培养的详细方案,可实现对雌性生殖干细胞微环境的长时间可视化。重要的是,该方案广泛适用于对具有多种感兴趣的荧光标记蛋白的生殖干细胞进行活体成像,这些蛋白可从库存中心和/或果蝇研究群体中获取。