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RhoA在小鼠卵母细胞生发泡破裂中的作用。

The role of RhoA in the germinal vesicle breakdown of mouse oocytes.

作者信息

Cheon Y P, Kim S W, Kim S J, Yeom Y I, Cheong C, Ha K S

机构信息

Biomolecule Research Team, Korea Basic Science Institute, Taejon, 305-333, Korea.

出版信息

Biochem Biophys Res Commun. 2000 Jul 14;273(3):997-1002. doi: 10.1006/bbrc.2000.3052.

Abstract

We have investigated a new role of RhoA in the germinal vesicle breakdown (GVBD) of mouse oocytes. First, RhoA was identified by immunostaining and ADP-ribosylation in germinal vesicle (GV) stage-oocytes. RhoA was mainly localized in the ooplasmic area, but rarely detected in germinal vesicle. Incubation of oocyte extract with C3 transferase induced a strong ADP-ribosylation at about 25 kDa. Incubation of GV-stage oocytes in culture medium induced the spontaneous maturation to GVBD by about 78 and 87% of total oocytes at 1 and 3 h, respectively. However, microinjection of C3 transferase into GV-stage oocytes significantly inhibited GVBD at 1 (GVBD = 29%) and 3 h (GVBD = 49%). To study the role of reactive oxygen species (ROS) in the oocyte maturation, the level of intra-oocyte ROS was measured using a ROS-specific fluorescent dye H(2)DCFDA during the oocyte maturation. Spontaneous maturation of GV-stage oocytes induced a significant increase of ROS at 3 h by about twofold over the control level and then the increased level was maintained until 6 h. However, microinjection of C3 transferase inhibited the production of intra-oocyte ROS. Incubation with ROS scavengers, N-acetyl-l-cysteine and catalase, blocked the ROS increase. The ROS scavengers also significantly inhibited GVBD, as did C3 transferase. Thus, it was proposed that RhoA was involved in the GVBD, possibly by the production of ROS in mouse oocytes.

摘要

我们研究了RhoA在小鼠卵母细胞生发泡破裂(GVBD)中的新作用。首先,通过免疫染色和ADP核糖基化在生发泡(GV)期卵母细胞中鉴定出RhoA。RhoA主要定位于卵质区域,但在生发泡中很少检测到。用C3转移酶孵育卵母细胞提取物会在约25 kDa处诱导强烈的ADP核糖基化。将GV期卵母细胞在培养基中孵育,分别在1小时和3小时时,约78%和87%的总卵母细胞会自发成熟至GVBD。然而,将C3转移酶显微注射到GV期卵母细胞中会在1小时(GVBD = 29%)和3小时(GVBD = 49%)时显著抑制GVBD。为了研究活性氧(ROS)在卵母细胞成熟中的作用,在卵母细胞成熟过程中使用ROS特异性荧光染料H(2)DCFDA测量卵母细胞内ROS的水平。GV期卵母细胞的自发成熟在3小时时导致ROS显著增加,比对照水平高出约两倍,然后增加的水平一直维持到6小时。然而,显微注射C3转移酶会抑制卵母细胞内ROS的产生。用ROS清除剂N-乙酰-L-半胱氨酸和过氧化氢酶孵育可阻止ROS的增加。ROS清除剂也显著抑制了GVBD,C3转移酶也是如此。因此,有人提出RhoA可能通过在小鼠卵母细胞中产生ROS参与GVBD。

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