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受精后海胆卵皮质层中荧光标记肌动蛋白的积累。

Accumulation of fluorescently labeled actin in the cortical layer in sea urchin eggs after fertilization.

作者信息

Hamaguchi Y, Mabuchi I

机构信息

Biological Laboratory, Tokyo Institute of Technology, Japan.

出版信息

Cell Motil Cytoskeleton. 1988;9(2):153-63. doi: 10.1002/cm.970090207.

Abstract

Actin from sea urchin eggs was fluorescently labeled with fluorescein isothiocyanate (FITC), N-(7-dimethylamino-4-methylcoumarinyl)-maleimide (DACM), or 5-iodoacetamidofluorescein (IAF) and microinjected into sea urchin eggs and oocytes. It distributed evenly in the cytoplasm of unfertilized eggs. Upon fertilization, actin accumulated first around the sperm binding site and, soon afterwards, in the fertilization cone. The accumulation propagated all over the cortex after a latent period of 10-20 sec. In the case of Clypeaster japonicus eggs, propagation of the accumulation coincided with a shape change in the egg, suggesting that the accumulated actin in the cortex generates forces. FITC-actin was incorporated into microvilli and retained in the cortex after cleavage. On the other hand, DACM- or IAF-actin was not incorporated into microvilli and was dispersed from the cortex by cleavage. These differences may be attributable to differences in the properties of the actins labeled at different sites. After photobleaching by laser light irradiation, FITC- or IAF-actin redistributed in the cortex of fertilized egg as quickly as it did before fertilization. When an unfertilized egg was injected with both actin and a calcium buffer (intracellular free Ca2+ concentration 9 microM), the actin accumulation was similar to that during fertilization but without the latent period. This suggests that the accumulation depended on the increase in the intracellular free Ca2+ concentration. When the unfertilized egg was injected with 0.2 M EGTA after injection of labeled actin and then inseminated, it accumulated only in the protrusion of cytoplasm where the sperm had entered, and fertilization was not completed. In immature oocytes, the accumulation was observed in the cortical region, including the huge protrusion of the cytoplasm where the sperm had entered. These results suggest that actin accumulation in the sperm binding site plays an important role in the sperm reception mechanism of the egg.

摘要

用异硫氰酸荧光素(FITC)、N-(7-二甲基氨基-4-甲基香豆素基)-马来酰亚胺(DACM)或5-碘乙酰氨基荧光素(IAF)对海胆卵中的肌动蛋白进行荧光标记,然后显微注射到海胆卵和卵母细胞中。它均匀分布在未受精卵的细胞质中。受精后,肌动蛋白首先在精子结合位点周围积累,随后不久在受精锥中积累。经过10 - 20秒的潜伏期后,积累物在整个皮质中扩散。对于日本笠海胆的卵,积累物的扩散与卵的形状变化同时发生,这表明皮质中积累的肌动蛋白产生了力。FITC-肌动蛋白在卵裂后被整合到微绒毛中并保留在皮质中。另一方面,DACM-或IAF-肌动蛋白没有被整合到微绒毛中,并且在卵裂时从皮质中分散。这些差异可能归因于在不同位点标记的肌动蛋白性质的差异。在激光照射进行光漂白后,FITC-或IAF-肌动蛋白在受精卵皮质中的重新分布与受精前一样快。当向未受精卵注射肌动蛋白和钙缓冲液(细胞内游离Ca2+浓度为9 microM)时,肌动蛋白的积累与受精时相似,但没有潜伏期。这表明积累依赖于细胞内游离Ca2+浓度的增加。当在注射标记肌动蛋白后向未受精卵注射0.2 M乙二醇双四乙酸(EGTA),然后进行授精时,它仅在精子进入的细胞质突起中积累,受精未完成。在未成熟卵母细胞中,在皮质区域观察到积累,包括精子进入的巨大细胞质突起。这些结果表明,精子结合位点处的肌动蛋白积累在卵的精子接收机制中起重要作用。

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