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Signaling pathways in ascidian oocyte maturation: The role of cyclic AMP and follicle cells in germinal vesicle breakdown

机译:海藻卵母细胞成熟中的信号传导途径:环状AMP和卵泡细胞在生小泡破裂中的作用

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Many ascidian oocytes undergo 'spontaneous' germinal vesicle breakdown (GVBD) when transferred from the ovary to normal pH 8.2 sea water (SW); however, low pH inhibits GVBD, which can then be stimulated while remaining in the low pH SW. Oocytes of Boltenia villosa blocked from GVBD by pH 4 SW undergo GVBD in response to permeant cyclic AMP (8-bromo-cyclic AMP), phosphodiesterase inhibitors (isobutylmethylxanthine and theophylline) or the adenylyl cyclase activator forskolin. This suggests that cAMP increases during GVBD. Removal of the follicle cells or addition of a protease inhibitor inhibits GVBD in response to raised pH but not to forskolin, theophylline or 8 bromo-cAMP. Isolated follicle cells in low pH SW release protease activity in response to an increase in pH. These studies imply that the follicle cells release protease activity, which either itself stimulates an increase in oocyte cAMP level or reacts with other molecules to stimulate this process. Studies with the mitogen-activated protein (MAP) kinase inhibitors U0126 and CI 1040 suggest that MAP kinase is not involved in GVBD. The Cdc25 inhibitor NSC 95397 inhibits GVBD at 200 nM in a reversible manner.
机译:当从卵巢转移至正常pH 8.2海水(SW)时,许多海鞘卵母细胞会经历“自发的”生胚囊泡分解(GVBD)。但是,低pH值会抑制GVBD,然后可以将其刺激,同时保持在低pH SW中。 pH 4 SW阻断GVBD的长毛丹螺卵母细胞通过渗透性环AMP(8-溴环AMP),磷酸二酯酶抑制剂(异丁基甲基黄嘌呤和茶碱)或腺苷酸环化酶激活剂forskolin经历GVBD。这表明在GVBD期间cAMP增加。去除卵泡细胞或添加蛋白酶抑制剂可响应pH升高而抑制GVBD,但不响应福司可林,茶碱或8 brom-cAMP。低pH SW中分离的卵泡细胞响应pH的增加而释放蛋白酶活性。这些研究暗示卵泡细胞释放蛋白酶活性,该蛋白酶活性本身刺激卵母细胞cAMP水平升高或与其他分子反应以刺激该过程。对促分裂原活化蛋白(MAP)激酶抑制剂U0126和CI 1040的研究表明,MAP激酶不参与GVBD。 Cdc25抑制剂NSC 95397以可逆方式抑制200 nM的GVBD。

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