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海胆受精卵周围细胞外基质的调节性胞吐作用与顺序构建。

Regulated exocytosis and sequential construction of the extracellular matrix surrounding the sea urchin zygote.

作者信息

Matese J C, Black S, McClay D R

机构信息

Developmental, Cell and Molecular Biology Group, Duke University, Durham, North Carolina 27708, USA.

出版信息

Dev Biol. 1997 Jun 1;186(1):16-26. doi: 10.1006/dbio.1997.8585.

Abstract

After fertilization most eggs become surrounded by a complex extracellular matrix. This study examines those matrix assembly processes that are triggered by fertilization of the sea urchin egg. The study uses antibodies that identify five different storage compartments in the egg. These compartments release their protein contents in a highly regulated fashion to assemble and modify the extraembryonic layers. The exocytosis sequence begins with a fertilization wave that progresses from the site of sperm entry and elevates the fertilization envelope above a water-filled perivitelline space. The immediate surface of the zygote then becomes covered by a newly secreted hyaline layer. Prior to fertilization some of the antigens are localized to cortical granules. Others are found in "basal laminar vesicles" that are released in a wave beginning at about 30 sec, or roughly at the same time as cortical granule exocytosis. The remaining antigens are exocytosed with a rather precise timing, but with a delay of several to tens of minutes relative to the first wave of exocytosis. "Apical vesicles," so named because antigens from this class are preferentially exocytosed toward the apical cell surface of polarized cells, include antigens that are exocytosed beginning at about 5 min postfertilization. The fourth compartment, named "echinonectin vesicles" release echinonectin, a protein that is deposited to the inner side of the hyaline layer. Surface staining of echinonectin is first detected about 10-15 min following sperm contact. Finally, maternal cadherin, which is stored in yet a fifth distinct compartment, is not detected on the surface until at least 30 min following fertilization. The data are also consistent with the notion that the tightly regulated timing of exocytosis contributes to the ordered assembly of the hyaline layer and elevation of the fertilization envelope. Finally, two of the vesicle classes continue to exocytose after the cells become polarized. In polarized cells apical and basal laminar antigens are trafficked toward opposite sides of the same cell after passing through the same trans-Golgi network-like compartment.

摘要

受精后,大多数卵子会被复杂的细胞外基质包围。本研究考察了由海胆卵受精引发的那些基质组装过程。该研究使用了能识别卵子中五个不同储存区室的抗体。这些区室以高度调控的方式释放其蛋白质成分,以组装和修饰胚外层。胞吐作用序列始于受精波,受精波从精子进入位点开始推进,并使受精膜在充满水的卵周隙上方升高。然后,合子的直接表面会被新分泌的透明层覆盖。受精前,一些抗原定位于皮质颗粒。其他抗原则存在于“基底层囊泡”中,这些囊泡在大约30秒时开始以波的形式释放,或者大致与皮质颗粒胞吐作用同时释放。其余抗原以相当精确的时间进行胞吐,但相对于第一波胞吐作用延迟了几分钟到几十分钟。“顶端囊泡”之所以这样命名,是因为这类抗原优先向极化细胞的顶端细胞表面胞吐,其中包括受精后约5分钟开始胞吐的抗原。第四个区室,即“棘皮粘连蛋白囊泡”,释放棘皮粘连蛋白,这种蛋白质沉积在透明层的内侧。精子接触后约10 - 15分钟首次检测到棘皮粘连蛋白的表面染色。最后,储存在第五个不同区室中的母体钙黏蛋白,直到受精后至少30分钟才在表面被检测到。这些数据也与这样一种观点一致,即严格调控的胞吐作用时间有助于透明层的有序组装和受精膜的升高。最后,两类囊泡在细胞极化后仍继续胞吐。在极化细胞中,顶端和基底层抗原在通过同一个类似反式高尔基体网络的区室后,被运输到同一细胞的相对两侧。

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