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小鼠胚胎致密化过程中钙作用的两个位点。

Two sites for calcium action in compaction of the mouse embryo.

作者信息

Bilozur M, Powers R D

出版信息

Exp Cell Res. 1982 Nov;142(1):39-45. doi: 10.1016/0014-4827(82)90406-2.

Abstract

Compact mouse morulae were decompacted in calcium-free medium and allowed to recompact in standard embryo culture medium. When the recompaction medium contained trifluoperazine (TFP)(0.05 mM), an inhibitor of the calcium-dependent protein calmodulin, the embryos failed to recompact. This effect could not be overcome by either db-cAMP (1.0 mM) or theophylline (0.75 mg/ml). When the recompaction medium contained less than standard calcium (0.085 or 0.17 mM) the embryos recompacted at a slower rate than in control medium (1.7 mM). The calcium ionophore A23187, at concentrations up to 1.5 X 10(-3) mM, had no significant stimulatory effect upon the recompaction rte of embryos in the reduced calcium medium. In addition, the calcium antagonist Verapamil (0.3 mM), which blocks calcium uptake by cells, significantly inhibited recompaction in standard culture medium. Large doses of diazepam inhibited recompaction only slightly in standard culture medium. Large doses of diazepam inhibited recompaction only slightly in standard culture medium. We conclude that calcium uptake into the cytoplasm is required for recompaction, but that cell surface calcium is also required and is rate-limiting under these experimental conditions.

摘要

致密的小鼠桑椹胚在无钙培养基中去致密化,然后在标准胚胎培养基中重新致密化。当重新致密化培养基中含有三氟拉嗪(TFP)(0.05 mM),一种钙依赖性蛋白钙调蛋白的抑制剂时,胚胎无法重新致密化。这种作用不能被二丁酰环磷腺苷(db - cAMP)(1.0 mM)或茶碱(0.75 mg/ml)克服。当重新致密化培养基中钙含量低于标准值(0.085或0.17 mM)时,胚胎重新致密化的速度比在对照培养基(1.7 mM)中慢。钙离子载体A23187,浓度高达1.5×10⁻³ mM时,对低钙培养基中胚胎的重新致密化速率没有显著的刺激作用。此外,钙拮抗剂维拉帕米(0.3 mM),它能阻止细胞摄取钙,在标准培养基中显著抑制重新致密化。大剂量地西泮在标准培养基中仅轻微抑制重新致密化。我们得出结论,重新致密化需要钙摄取到细胞质中,但细胞表面钙也是必需的,并且在这些实验条件下是限速因素。

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