新的即時成像、非侵入性細胞標記技術 發現
2 細胞階段胚胎只有只有其中一個細胞
會演化成80% 胚胎主體 未來的外胚層 內胚層(卵黃囊)和滋養外胚層(胎盤)
Labeling and live imaging of human embryos reveal that the majority of the future body originates, mostly, from one of the 2-cell stage blastomeres. Descendants of the first 2-cell stage blastomere to divide contribute more asymmetric divisions at the 8-cell stage, which generate the small number of founding epiblast cells before implantation.
https://www.cell.com/action/showPdf?pii=S0092-8674%2824%2900455-0
The first two blastomeres contribute unequally
to the human embryo
https://doi.org/10.1016/j.cell.2024.04.029
SUMMARY
Retrospective lineage reconstruction of humans predicts that dramatic clonal imbalances in the body can be
traced to the 2-cell stage embryo. However, whether and how such clonal asymmetries arise in the embryo is
unclear. Here, we performed prospective lineage tracing of human embryos using live imaging, non-invasive
cell labeling, and computational predictions to determine the contribution of each 2-cell stage blastomere to
the epiblast (body), hypoblast (yolk sac), and trophectoderm (placenta). We show that the majority of epiblast
cells originate from only one blastomere of the 2-cell stage embryo. We observe that only one to three cells
become internalized at the 8-to-16-cell stage transition. Moreover, these internalized cells are more
frequently derived from the first cell to divide at the 2-cell stage. We propose that cell division dynamics
and a cell internalization bottleneck in the early embryo establish asymmetry in the clonal composition of
the future human body.