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林蛙卵母细胞第一次减数分裂过程中孕酮诱导的质膜去极化的生化关联

Biochemical correlates of progesterone-induced plasma membrane depolarization during the first meiotic division in Rana oocytes.

作者信息

Morrill G A, Ziegler D H, Kunar J, Weinstein S P, Kostellow A B

出版信息

J Membr Biol. 1984;77(3):201-12. doi: 10.1007/BF01870569.

Abstract

Changes in protein synthesis, protein phosphorylation and lipid phosphorylation in the amphibian oocyte plasma membrane have been correlated with electrical changes following steroid induction of the completion of the first meiotic division. The oocyte first depolarizes from about -60 mV (inside negative) to about -25 mV 1 to 2 hr before breakdown of the large nucleus followed by a further depolarization beginning 3 to 6 hr after nuclear breakdown. The initial depolarization is associated with appearance of previously described cycloheximide-sensitive cytoplasmic factor(s) which induce both nuclear breakdown and plasma membrane depolarization. We found a similar ED50 (0.4 microM) for cycloheximide inhibition of nuclear breakdown, membrane depolarization, and [3H]-leucine incorporation. Emetine (1 nM to 1 mM) was inactive. The period of cycloheximide sensitivity (first 5 hr) is essentially the same for plasma membrane depolarization and nuclear breakdown. The onset of the second depolarization phase following nuclear breakdown is associated with a marked increase in the rate of [3H]-leucine and [32PO4] incorporation into membrane protein and lipid. Polyacrylamide gel electrophoresis of membrane protein and lipoprotein indicated that a major newly synthesized membrane component is proteolipid. An increase in [32PO4] incorporation into membrane phosphatidylserine and phosphatidylethanolamine (with a decrease in phosphatidylcholine [32PO4] begins during the second depolarization phase and coincides with the appearance of excitability in the oocyte plasma membrane. In toto, the bulk of the biochemical changes (proteins, phosphoproteins, proteolipids, phospholipids) appear to be associated with plasma membrane components and coincide with stepwise changes in membrane permeability to specific ions (e.g. Cl-).

摘要

两栖类卵母细胞质膜中蛋白质合成、蛋白质磷酸化和脂质磷酸化的变化,已与甾体诱导第一次减数分裂完成后的电变化相关联。在大核破裂前1至2小时,卵母细胞首先从约-60 mV(内负)去极化至约-25 mV,随后在核破裂后3至6小时开始进一步去极化。初始去极化与先前描述的对放线菌酮敏感的细胞质因子的出现有关,该因子诱导核破裂和质膜去极化。我们发现放线菌酮抑制核破裂、膜去极化和[3H] - 亮氨酸掺入的ED50相似(0.4 microM)。依米丁(1 nM至1 mM)无活性。质膜去极化和核破裂对放线菌酮敏感的时期(最初5小时)基本相同。核破裂后第二个去极化阶段的开始与[3H] - 亮氨酸和[32PO4]掺入膜蛋白和脂质的速率显著增加有关。膜蛋白和脂蛋白的聚丙烯酰胺凝胶电泳表明,一种主要的新合成膜成分是蛋白脂质。在第二个去极化阶段,[32PO4]掺入膜磷脂酰丝氨酸和磷脂酰乙醇胺增加(同时磷脂酰胆碱[32PO4]减少),并与卵母细胞质膜兴奋性的出现同时发生。总体而言,大部分生化变化(蛋白质、磷蛋白、蛋白脂质、磷脂)似乎与质膜成分有关,并与膜对特定离子(如Cl-)通透性的逐步变化一致。

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