A quantification model for apoptosis in mouse embryos in the early stage of fetation.

PengFei Wang, JianHua Fu, WanYun Ma, DieYan Chen, DanYu Lü, WenJia Bai
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引用次数: 1

Abstract

Apoptosis is the most important inducement and modulator for embryos in the early stage of fetation, i.e. after the 8-cell stage, mostly the morula and blastula stage, to proceed to the stage of nonlinear development. Using a two-photon laser scanning microscopy (TPLSM) system, we obtained 3-dimensional (3D) fluorescent images of preimplantation mouse embryos. A model for quantification was established. The statistical results for the spatial location of apoptosis bodies in embryos was obtained following image processing, as well as investigation of the kinetics of apoptosis. It was found that most (70%) apoptosis occurred in the trophectoderm, and the departure between the centroid and geometric center of embryos had a step transition when embryos developed into the 32-cell stage, which was consistent with the theoretical prediction that the blastocele would induce a symmetry break of the distribution of cells in embryos.

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胚胎早期小鼠胚胎细胞凋亡定量模型的建立。
细胞凋亡是胚胎早期,即8细胞期(主要是桑葚胚期)以后进入非线性发育阶段的最重要的诱导因子和调节剂。利用双光子激光扫描显微镜(TPLSM)系统,我们获得了小鼠胚胎着床前的三维荧光图像。建立了定量模型。通过图像处理和细胞凋亡动力学研究,得到胚胎细胞凋亡小体空间定位的统计结果。结果表明,大多数(70%)细胞凋亡发生在滋养外胚层,胚胎质心与几何中心的偏离在胚胎发育至32细胞期时发生了阶梯过渡,这与理论预测胚泡发育会导致胚胎细胞分布的对称性断裂一致。
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