Effects of Cytochalasin-D on the Maintenance of Blastocoels of Bovine Blastocysts Produced In Vitro

Y. Tsuzuki, K. Ashizawa, N. Fujihara
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引用次数: 1

Abstract

In the present study, we investigated the role of actin filaments in the blastocoel (BC) of bovine blastocysts produced in vitro by using cytochalasin-D (CD), an inhibitor of actin polymerization. Blastocysts classified as good or poor based on their morphological normality were exposed to 2 μM CD for 1.5-2 hr. After incubation, the presence or absence of BC was observed, and the re-expansion rate was assessed after transferring CD-treated blastocysts with collapsed BC to a non-CD medium. Ultrastructural observation was also undertaken using a transmission electron microscope (TEM). The remaining blastocysts were immersed in a hypotonic solution of sodium citrate so that the cells could be counted to confirm the classification grade of blastocysts in this study. The percent of maintained BC under the presence of CD in the good group was significantly lower (P<0.05) than that in the poor group (3.3% versus 27.7%, respectively). The average cell number of blastocysts in the good group was significantly more (P<0.05) than that in the poor group. In addition, when the blastocysts with shrunken BC in both groups were cultured, re-expansion rates in the good and poor groups were 83.3 and 75.0%, respectively, and no significant difference was observed between groups. Based on observation of the ultrastructure with TEM, the microvilli on the surface of some trophoblast cells of some blastocysts in the poor group in the presence of CD showed a translucent matrix, and their electron density was low compared with that of trophoblast cells of blastocysts in the good and non-treated (control) groups. However, the electron density of microvilli after removal of CD in the poor group increased to a level comparable to those of the good and control groups. These results suggest that polymerizing actin may be required to sustain the blastocoel and microvilli of blastocysts produced in vitro. However, in poor grade blastocysts, the polymerization ability of actin present in the filamentous form in the microvilli in some cells might be lower than that in good grade blastocysts.
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细胞松弛素d对体外培养的牛囊胚胚腔维持的影响
在本研究中,我们利用细胞松弛素d (cytochalasin-D,一种肌动蛋白聚合抑制剂)研究了肌动蛋白丝在体外培养的牛囊胚囊胚(BC)中的作用。将形态学正常的囊胚分为好囊胚和差囊胚,置于2 μM CD环境中1.5 ~ 2小时。孵育后,观察BC的存在或不存在,并将具有塌陷BC的cd处理囊胚转移到非cd培养基后评估再膨胀率。透射电镜(TEM)进行超微结构观察。将剩余囊胚浸泡在柠檬酸钠低渗溶液中计数,以确定本研究囊胚的分类等级。良好组在CD存在下维持BC的百分比显著低于不良组(分别为3.3%和27.7%)(P<0.05)。良好组囊胚平均细胞数显著高于不良组(P<0.05)。此外,两组BC萎缩胚培养时,良好组和不良组的再膨胀率分别为83.3%和75.0%,两组间差异无统计学意义。透射电镜观察超微结构发现,在CD作用下,不良组部分囊胚滋养层细胞表面微绒毛呈半透明基质,其电子密度较良好组和未处理组囊胚滋养层细胞低。然而,去除CD后,不良组微绒毛的电子密度增加到与良好组和对照组相当的水平。这些结果表明,肌动蛋白的聚合可能需要维持囊胚胚腔和微绒毛的体外培养。然而,在低级别囊胚中,某些细胞微绒毛中以丝状形式存在的肌动蛋白聚合能力可能低于高级别囊胚。
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