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衣藻受精过程中细胞黏附丧失的快速和慢速机制。

Rapid and slow mechanisms for loss of cell adhesiveness during fertilization in Chlamydomonas.

作者信息

Hunnicutt G R, Snell W J

机构信息

Department of Cell Biology and Neuroscience, University of Texas Southwestern Medical Center, Dallas 75235.

出版信息

Dev Biol. 1991 Sep;147(1):216-24. doi: 10.1016/s0012-1606(05)80019-3.

Abstract

Although vegetative cells, gametes, and zygotes of the biflagellated alga Chlamydomonas bear flagella, only the flagella of mt+ and mt- gametes are adhesive. The molecules responsible for adhesiveness, mt+ and mt- agglutinins, are long rod-shaped glycoproteins displayed on the flagellar membrane. These flagellar agglutinins, which gametes use both as adhesion and signaling molecules during the early events of fertilization, are lost from the flagella during adhesion. Flagellar adhesiveness can be maintained, however, by recruitment and activation of preexisting, inactive agglutinins from the plasma membrane of the cell body (Hunnicutt et al, 1990, J. Cell Biol. 111, 1605-1616) unless the gametes of opposite mating types fuse to form zygotes. Upon cell fusion, flagellar adhesiveness is lost. In the studies presented here, we have employed an in vitro bioassay to measure agglutinins in both cell bodies and flagella at various times during gametogenesis, during fertilization, and after zygote-formation. By use of the bioassay, which can detect agglutinins that are functionally inactive in vivo, we found that vegetative cells are devoid of agglutinins. These adhesion molecules appear only after gametogenesis is underway with the cell body agglutinins appearing first and then the flagellar agglutinins. Surprisingly, 30 min after zygote formation, when the zygotes' flagella are no longer adhesive, the flagellar agglutinin activity detectable with the bioassay remains high. One interpretation of these results is that zygotes continue to recruit agglutinins from the cell body to the flagella, but cell fusion abrogates activation of the agglutinins. Within 45-90 min after fusion both the cell body and flagellar agglutinins are lost and can be detected in the medium. These mechanisms, which render the zygotes nonadhesive to other zygotes and unmated gametes, contribute to the Chlamydomonas equivalent of a block to polyspermy.

摘要

尽管双鞭毛藻类衣藻的营养细胞、配子和合子都带有鞭毛,但只有正交配型(mt+)和负交配型(mt-)配子的鞭毛具有黏附性。负责黏附性的分子,即mt+和mt-凝集素,是展示在鞭毛膜上的长杆状糖蛋白。这些鞭毛凝集素在受精早期事件中既作为黏附分子也作为信号分子被配子利用,在黏附过程中会从鞭毛上消失。然而,除非相反交配型的配子融合形成合子,否则鞭毛的黏附性可以通过从细胞体的质膜募集和激活预先存在的无活性凝集素来维持(Hunnicutt等人,1990年,《细胞生物学杂志》111卷,1605 - 1616页)。细胞融合后,鞭毛的黏附性丧失。在本文所呈现的研究中,我们采用了一种体外生物测定法来测量在配子发生、受精过程以及合子形成后的不同时间,细胞体和鞭毛中的凝集素。通过使用这种能够检测在体内功能无活性的凝集素的生物测定法,我们发现营养细胞不含凝集素。这些黏附分子仅在配子发生开始后出现,细胞体凝集素先出现,然后是鞭毛凝集素。令人惊讶的是,在合子形成30分钟后,当合子的鞭毛不再具有黏附性时,用生物测定法可检测到的鞭毛凝集素活性仍然很高。对这些结果的一种解释是,合子继续从细胞体向鞭毛募集凝集素,但细胞融合消除了凝集素的激活。在融合后45 - 90分钟内,细胞体和鞭毛凝集素都消失了,并能在培养基中检测到。这些使合子对其他合子和未交配配子不具有黏附性的机制,有助于衣藻实现相当于多精受精阻断的过程。

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