al-Obaidi N, Kastner U, Merker H J, Klug S
Institut für Toxikologie und Embryopharmakologie, Freie Universität Berlin, Germany.
Arch Toxicol. 1995;69(7):472-9. doi: 10.1007/s002040050201.
On the basis of an already established suspension organ culture system of mouse palate anlagen, we developed a corresponding culture system for rat palate anlagen. In order to optimize the culture results we systematically studied the influence of main "culture conditions" such as dissection technique, rotation speed, gassing schedule, and developmental stage at the onset of culture for mice and rat palate anlagen. This system allows culturing rat palate anlagen from day 15 of gestation to day 18 + 8 h (80 h) under serum- and antibiotic-free conditions using a chemically defined medium, resulting in 90% fused palates. The explants, containing the maxillary vault and the palatal shelves, were cultured in siliconized culture flasks at a rotation speed of 12 rpm and a temperature of 37 degrees C (Table 1).
基于已建立的小鼠腭原基悬浮器官培养系统,我们开发了相应的大鼠腭原基培养系统。为了优化培养结果,我们系统地研究了主要“培养条件”的影响,如解剖技术、转速、通气方案以及小鼠和大鼠腭原基培养开始时的发育阶段。该系统允许在无血清和抗生素的条件下,使用化学成分明确的培养基,将大鼠腭原基从妊娠第15天培养至第18 + 8小时(80小时),腭融合率达90%。含有上颌穹窿和腭板的外植体在硅化培养瓶中以12转/分钟的转速和37摄氏度的温度进行培养(表1)。