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首页> 外文期刊>Development >Cortical granule translocation is microfilament mediated and linked to meiotic maturation in the sea urchin oocyte.
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Cortical granule translocation is microfilament mediated and linked to meiotic maturation in the sea urchin oocyte.

机译:皮质颗粒易位是微丝介导的,并与海胆卵母细胞的减数分裂成熟有关。

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Cortical granules exocytose after the fusion of egg and sperm in most animals, and their contents function in the block to polyspermy by creating an impenetrable extracellular matrix. Cortical granules are synthesized throughout oogenesis and translocate en masse to the cell surface during meiosis where they remain until fertilization. As the mature oocyte is approximately 125 micro m in diameter (Lytechinus variegatus), many of the cortical granules translocate upwards of 60 micro m to reach the cortex within a 4 hour time window. We have investigated the mechanism of this coordinated vesicular translocation event. Although the stimulus to reinitiate meiosis in sea urchin oocytes is not known, we found many different ways to reversibly inhibit germinal vesicle breakdown, and used these findings to discover that meiotic maturation and cortical granule translocation are inseparable. We also learned that cortical granule translocation requires association with microfilaments but not microtubules. It is clear from endocytosis assays that microfilament motors are functional prior to meiosis, even though cortical granules do not use them. However, just after GVBD, cortical granules attach to microfilaments and translocate to the cell surface. This latter conclusion is based on organelle stratification within the oocyte followed by positional quantitation of the cortical granules. We conclude from these studies that maturation promoting factor (MPF) activation stimulates vesicle association with microfilaments, and is a key regulatory step in the coordinated translocation of cortical granules to the egg cortex.
机译:在大多数动物中,卵与精子融合后,皮质颗粒会胞吐,其含量通过形成难以穿透的细胞外基质而在多精子的阻滞中起作用。皮质颗粒是在整个卵子发生过程中合成的,并在减数分裂期间大量转运至细胞表面,并一直保留直至受精。由于成熟卵母细胞的直径约为125微米(Lytechinus variegatus),因此许多皮质颗粒向上移位60微米,在4小时的时间范围内到达皮质。我们已经研究了这种协调的水泡易位事件的机制。尽管尚不清楚刺激海胆卵母细胞恢复减数分裂的刺激方法,但我们发现了许多可逆性抑制生小泡破裂的方法,并利用这些发现发现减数分裂成熟和皮质颗粒易位是不可分割的。我们还了解到,皮质颗粒易位需要与微丝相关,而与微管无关。从内吞作用测定法可以清楚地看出,即使皮质颗粒不使用微丝马达,减数分裂前的微丝马达仍然起作用。但是,刚好在GVBD之后,皮质颗粒附着在微丝上并转移到细胞表面。后一个结论是基于卵母细胞内的细胞器分层,然后是皮质颗粒的位置定量。我们从这些研究中得出结论,成熟促进因子(MPF)激活可刺激囊泡与微丝缔合,并且是皮层颗粒向蛋皮层协调移位的关键调控步骤。

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