Eight-cell Embryo

An eight-cell embryo is an early stage of embryonic development in which the fertilized egg has divided into eight smaller cells, or blastomeres, making it an important landmark in developmental biology and reproductive science. It forms through cleavage, a series of rapid mitotic divisions that partition the original cytoplasm without substantially increasing the embryo’s overall size; around this stage, blastomeres begin strengthening cell-cell contacts and may undergo compaction. Studying eight-cell embryos helps researchers evaluate early development, investigate embryo quality in assisted reproduction, and examine how cell division, gene activity, and organization establish the foundation for later morula and blastocyst formation.

Eight-cell Embryo - Related Videos

Research

JoVE Journal - Biology
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Xenotransplantation of Human Stem Cells into the Chicken Embryo

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Cited by 31 •

2010

In this paper we present a method for transplanting human stem cells into various regions of the central nervous system of the chicken embryo. This provides an in vivo model for assessing the proliferation and differentiation of various types of human stem cells in embryonic tissue environments.

Research

JoVE Journal - Developmental Biology

Isolation and Characterization of Single Cells from Zebrafish Embryos

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Cited by 20 •

2016

This protocol describes a method for isolating single cells from zebrafish embryos, enriching for cells of interest, capturing zebrafish cells in microfluidic based single cell multiplex systems, and assessing gene expression from single cells.

Imaging Cell Shape Change in Living Drosophila Embryos

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Cited by 23 •

2011

Early development of the fruit fly, Drosophila melanogaster, is characterized by a number of cell shape changes that are well suited for imaging approaches. This article will describe basic tools and methods required for live confocal imaging of Drosophila embryos, and will focus on a cell shape change called cellularization.

Single Cell Transfection in Chick Embryos

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Cited by 3 •

2010

Using fine tip micropipettes we inject plasmid DNA into subdomains of chicken somites or neural tubes. The concentration of the plasmid is adjusted to generate single transfected cells. We then allow the cells to develop into clonal populations.

Use of LysoTracker to Detect Programmed Cell Death in Embryos and Differentiating Embryonic Stem Cells

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Cited by 53 •

2012

We present a simple protocol to visualize regions of programmed cell death (PCD) in mouse embryos and differentiating embryonic stem (ES) cell cultures using a highly soluble dye called LysoTracker.

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