Hoshino Y, Nishino E, Mii M
Laboratory of Plant Cell Technology, Faculty of Horticulture, Chiba University, 648 Matsudo, Matsudo City, Chiba Pref. 271-8510, Japan, , , , , , JP.
Laboratory of Plant Morphology, Faculty of Horticulture, Chiba University, 648 Matsudo, Matsudo City, Chiba Pref. 271-8510, Japan, , , , , , JP.
Plant Cell Rep. 2000 Apr;19(5):443-447. doi: 10.1007/s002990050753.
Mature ovules of Dianthus (Caryophyllaceae) were histologically observed by clearing and serial sectioning to characterize the cells of the embryo sac. The results show that the mature embryo sac was located deep inside the hemitropous ovule due to thick nucellar tissue at the micropylar region. For the isolation of the embryo sacs, ovules were collected from ovaries of flowers 1 day after anthesis, and treated with an enzyme solution for digesting cell walls on a gyratory shaker. After 12 h of enzyme treatment, these ovules were dissected using a glass needle under an inverted microscope to release the embryo sacs. The embryo sacs, characterized by their specific size, were successfully released by these successive treatments. The viability of the embryo sacs was more than 80% as assessed with fluorescein diacetate staining. Fluorescent staining with 4,6-diamidino-2-phenylindole revealed the nuclei of the egg apparatus in the isolated embryo sacs. The procedure for isolating embryo sacs established in this study will offer a new approach to further in vitro studies on fertilization in Dianthus.
通过透明和连续切片的方法对石竹科石竹属植物成熟胚珠进行组织学观察,以表征胚囊细胞。结果表明,由于珠孔区域的珠心组织较厚,成熟胚囊位于半倒生胚珠的深处。为了分离胚囊,在花开放后1天从子房收集胚珠,并在回转摇床上用酶溶液处理以消化细胞壁。酶处理12小时后,在倒置显微镜下用玻璃针解剖这些胚珠以释放胚囊。通过这些连续处理成功释放了具有特定大小特征的胚囊。用荧光素二乙酸酯染色评估,胚囊的活力超过80%。用4,6-二脒基-2-苯基吲哚进行荧光染色揭示了分离胚囊中卵器的细胞核。本研究中建立的胚囊分离程序将为石竹属植物受精的进一步体外研究提供一种新方法。