Literature DB >> 9266770

Ascidian eggs block polyspermy by two independent mechanisms: one at the egg plasma membrane, the other involving the follicle cells.

C Lambert1, H Goudeau, C Franchet, G Lambert, M Goudeau.   

Abstract

Many ascidians live in clumps and usually release sperm before the eggs. Consequently, eggs are often spawned into dense clouds of sperm. Because fertilization by more than a single sperm is lethal, ascidians have evolved at least two successive blocks to polyspermy: the rapid release of a glycosidase that inhibits sperm binding to the vitelline coat (VC) and a subsequent change in membrane potential that prevents supernumerary sperm-egg fusion. This paper shows that (1) these two blocks can be uncoupled by the use of suramin, and (2) most of the glycosidase appears to be from the follicle cells, which are accessory cells on the outside of the egg VC. Phallusia mammillata eggs initially bind numerous sperm but, after the glycosidase is released, only a few additional sperm bind. Intact eggs in 20 microM suramin release glycosidase, but the electrical response is inhibited; sperm swim actively and bind to the VC but fail to penetrate. Suramin treatment is completely reversible; intact eggs exhibit the electrical response an average of 11 minutes after the drug is washed out. Sperm must contact the follicle cells before passing through the VC; eggs with the VC removed and fertilized in the presence of 20 microM suramin show the electrical response 35% of the time, thus VC removal enhances sperm entry. Like the intact eggs, 100% of the naked eggs respond electrically to fertilization after the drug is washed out. Follicle cells that are isolated by calcium magnesium free seawater and then returned to complete seawater release N-acetylglucosaminidase activity in response to sperm. Thus, these eggs have two blocks to polyspermy that operate in sequence: an early first block resulting from enzymatic modification of the VC by N-acetylglucosaminidase released primarily from follicle cells and a second electrical block operating at the egg plasma membrane level and requiring sperm-egg fusion.

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Year:  1997        PMID: 9266770     DOI: 10.1002/(SICI)1098-2795(199709)48:1<137::AID-MRD16>3.0.CO;2-Y

Source DB:  PubMed          Journal:  Mol Reprod Dev        ISSN: 1040-452X            Impact factor:   2.609


  5 in total

Review 1.  Calcium at fertilization and in early development.

Authors:  Michael Whitaker
Journal:  Physiol Rev       Date:  2006-01       Impact factor: 37.312

2.  Localization of ubiquitin C-terminal hydrolase L1 in mouse ova and its function in the plasma membrane to block polyspermy.

Authors:  Satoshi Sekiguchi; Jungkee Kwon; Etsuko Yoshida; Hiroko Hamasaki; Shizuko Ichinose; Makoto Hideshima; Mutsuki Kuraoka; Akio Takahashi; Yoshiyuki Ishii; Shigeru Kyuwa; Keiji Wada; Yasuhiro Yoshikawa
Journal:  Am J Pathol       Date:  2006-11       Impact factor: 4.307

3.  Inactivation kinetics of formaldehyde on N-acetyl-β-D-glucosaminidase from Nile tilapia (Oreochromis niloticus).

Authors:  Wei-Ni Zhang; Ding-Ping Bai; Xin-Yu Lin; Qing-Xi Chen; Xiao-Hong Huang; Yi-Fan Huang
Journal:  Fish Physiol Biochem       Date:  2013-09-15       Impact factor: 2.794

4.  Reproductive protein evolution in two cryptic species of marine chordate.

Authors:  Marie L Nydam; Richard G Harrison
Journal:  BMC Evol Biol       Date:  2011-01-19       Impact factor: 3.260

Review 5.  Mechanisms of Sperm-Egg Interactions: What Ascidian Fertilization Research Has Taught Us.

Authors:  Hitoshi Sawada; Takako Saito
Journal:  Cells       Date:  2022-07-01       Impact factor: 7.666

  5 in total

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