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肌醇1,4,5 -三磷酸诱导金黄仓鼠卵的钙释放以及鸟嘌呤核苷酸结合蛋白介导的周期性钙升高。

Inositol 1,4,5-trisphosphate-induced calcium release and guanine nucleotide-binding protein-mediated periodic calcium rises in golden hamster eggs.

作者信息

Miyazaki S

机构信息

Department of Physiology, Jichi Medical School, Tochigi-ken, Japan.

出版信息

J Cell Biol. 1988 Feb;106(2):345-53. doi: 10.1083/jcb.106.2.345.

DOI:10.1083/jcb.106.2.345
PMID:3123497
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2114965/
Abstract

Periodic increases in intracellular free calcium occur upon fertilization of golden hamster eggs (Miyazaki et al. 1986. Dev. Biol. 118:259-267). To investigate the underlying mechanism, inositol 1,4,5-trisphosphate (IP3) and guanine nucleotides were microinjected into the egg while Ca2+ transients were monitored by aequorin luminescence and/or hyperpolarization in the membrane potential, which indicates the exact timing and spatial distribution of the Ca2+ rise. Injection of IP3 induced an immediate Ca2+ transient of 13-18 s in the entire egg. The critical concentration of IP3 was 80 nM in the injection pipette (2 nM in the egg, assuming uniform distribution); the effect was all-or-none. The Ca2+ rise occurred even in Ca-free external medium. Injection of 5 mM GTP or 0.33 mM guanosine-5'-O-(3-thiotriphosphate) (GTP gamma S) (calculated intracellular concentration, 200 or 12 microM, respectively) caused a similar Ca2+ transient with a delay of 160-200 s. More than 50 microM GTP gamma S produced recurring and attenuating Ca2+ transients in a local area of the cytoplasm, with an initial delay of 25-40 s and intervals of 45-60 s. In Ca-free medium the first one to two Ca2+ transients occurred but succeeding ones were absent. Preinjection of guanosine-5'-O-(2-thiodiphosphate) inhibited the occurrence of both GTP gamma S-induced and sperm-induced Ca2+ transients in a dose-dependent manner. Neither pertussis nor cholera toxins had effect. It was proposed that sperm-egg interaction activates a GTP-binding protein that stimulates production of IP3, causing the first one to two Ca releases from internal stores, and also stimulates a pathway for elevation of Ca2+ permeability in the plasma membrane, thereby sustaining the repeated Ca2+ releases.

摘要

金黄地鼠卵受精后,细胞内游离钙会周期性增加(宫崎等人,1986年。《发育生物学》118:259 - 267)。为了探究其潜在机制,将肌醇1,4,5 - 三磷酸(IP3)和鸟嘌呤核苷酸显微注射到卵中,同时通过水母发光蛋白发光和/或膜电位超极化监测Ca2+瞬变,这表明了Ca2+升高的确切时间和空间分布。注射IP3会在整个卵中立即引发13 - 18秒的Ca2+瞬变。注射移液器中IP3的临界浓度为80 nM(假设均匀分布,卵内为2 nM);其效应是全或无的。即使在无钙的外部介质中也会出现Ca2+升高。注射5 mM GTP或0.33 mM鸟苷 - 5'-O -(3 - 硫代三磷酸)(GTPγS)(计算得出的细胞内浓度分别为200或12 μM)会引发类似的Ca2+瞬变,但有160 - 200秒的延迟。超过50 μM的GTPγS会在细胞质局部区域产生反复且衰减的Ca2+瞬变,初始延迟为25 - 40秒,间隔为45 - 60秒。在无钙介质中,最初的一到两个Ca2+瞬变会出现,但后续的则不会。预先注射鸟苷 - 5'-O -(2 - 硫代二磷酸)会以剂量依赖的方式抑制GTPγS诱导的和精子诱导的Ca2+瞬变的发生。百日咳毒素和霍乱毒素均无作用。有人提出,精卵相互作用会激活一种GTP结合蛋白,该蛋白会刺激IP3的产生,导致从内部储存库中首次释放一到两个Ca2+,并且还会刺激质膜中Ca2+通透性升高的途径,从而维持Ca2+的反复释放。

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本文引用的文献

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Fertilization potential in golden hamster eggs consists of recurring hyperpolarizations.金黄仓鼠卵的受精潜能由反复出现的超极化组成。
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Micro-injection of inositol 1,3,4,5-tetrakisphosphate activates sea urchin eggs by a mechanism dependent on external Ca2+.微量注射肌醇1,3,4,5 - 四磷酸通过一种依赖于细胞外钙离子的机制激活海胆卵。
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Inositol(1,3,4,5)tetrakisphosphate-induced activation of sea urchin eggs requires the presence of inositol trisphosphate.肌醇(1,3,4,5)四磷酸诱导的海胆卵激活需要三磷酸肌醇的存在。
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The part played by inositol trisphosphate and calcium in the propagation of the fertilization wave in sea urchin eggs.肌醇三磷酸和钙在海胆卵受精波传播中所起的作用。
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