Dorresteijn Adriaan W C, Wagemaker Huibert A, de Laat Siegfried W, van den Biggelaar Jo A M
Zoological Laboratory, State University of Utrecht, Padualaan 8, 3508 TB, Utrecht, The Netherlands.
Hubrecht Laboratory, International Embryological Institute, Uppsalalaan 8, 3584 CT, Utrecht, The Netherlands.
Wilehm Roux Arch Dev Biol. 1983 Sep;192(5):262-269. doi: 10.1007/BF00848658.
During the early development of the molluscPatella, the dorsoventral axis is established after the fifth cleavage due to direct interaction between the animal micromeres and one of the vegetal macromeres. This vegetal macromere is thereby induced to become the mesentoblast mother cell (3D). In this study we have examined intercellular communication in earlyPatella embryos by monitoring the transfer of the fluorescent dye, Lucifer Yellow, upon iontophoretic injection into blastomeres between the second and sixth cleavage. Up to the fifth cleavage dye transfer is detectable neither inin toto embryos nor in serial sections. Shortly after the fifth cleavage dye-coupling between blastomeres becomes apparent. This occurs approximately 40 min before the interaction between animal micromeres and the future mesentoblast mother cell. Inspection of serially sectioned embryos after dye-iontophoresis in either animal micromeres or in the central macromere 3D showed the absence of direct dye-transfer between these cells at the stage of interaction. The reduced rate of dye-transfer from the 3D macromere to its dorsal neighbour 2d suggests a bilateral symmetrical transfer pattern, the axis of which corresponds with the dorsoventral axis at the sixth cleavage. Cell deletion experiments demonstrated that the establishment of dye-coupling between the vegetal macromeres occurs independently of the interaction between animal and vegetal blastomeres.
在软体动物笠贝的早期发育过程中,由于动物极微裂球与一个植物极大裂球之间的直接相互作用,背腹轴在第五次卵裂后确立。这个植物极大裂球因此被诱导成为中胚层母细胞(3D)。在本研究中,我们通过监测荧光染料路西法黄在离子电渗注入第二次至第六次卵裂的卵裂球后在早期笠贝胚胎中的转移情况,来研究细胞间通讯。在第五次卵裂之前,无论是在完整胚胎还是在连续切片中都检测不到染料转移。在第五次卵裂后不久,卵裂球之间的染料偶联变得明显。这大约发生在动物极微裂球与未来的中胚层母细胞相互作用前40分钟。在动物极微裂球或中央大裂球3D中进行染料离子电渗后,对连续切片胚胎的检查显示,在相互作用阶段,这些细胞之间不存在直接的染料转移。从3D大裂球到其背侧相邻细胞2d的染料转移速率降低,表明存在双侧对称的转移模式,其轴与第六次卵裂时的背腹轴相对应。细胞缺失实验表明,植物极大裂球之间染料偶联的建立独立于动物极和植物极卵裂球之间的相互作用。