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Tail reduction process during human embryonic development.

Sayaka Tojima1,2, Haruyuki Makishima3, Tetsuya Takakuwa4

  • 1Department of Anatomy and Cell Biology, Graduate School of Medicine, Osaka City University, Osaka, Japan.

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|January 10, 2018
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Summary
This summary is machine-generated.

Human embryonic development involves tail formation, followed by reduction. This study visualizes somite changes, revealing a common tail reduction mechanism in amniotes and insights into human tail anomalies.

Keywords:
amniotesevolutionsomitetailthree-dimensional reconstruction

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Area of Science:

  • Developmental Biology
  • Evolutionary Biology
  • Human Anatomy

Background:

  • Embryonic development in humans includes a transient tail, similar to other amniotes.
  • The evolutionary process of human tail reduction remains unclear.
  • Congenital 'human tail' anomalies are poorly understood, with their link to embryonic tails unverified.

Purpose of the Study:

  • To develop a novel method for visualizing all somites in embryonic development.
  • To investigate the process of tail reduction during human embryonic development.
  • To explore potential common mechanisms of tail morphogenesis in amniotes.

Main Methods:

  • Utilized sagittal-sectioned human embryos from Carnegie Stage (CS) 13 to CS23.
  • Employed photomicroscopy and 3D reconstruction techniques.
  • Visualized and labeled all somites within the developing embryos.

Main Results:

  • Successfully visualized and labeled somites in human embryos.
  • Observed a peak in somite number at CS16, followed by a significant decrease of approximately five somites.
  • Identified tail reduction correlating with somite decrease, mirroring patterns in short-tailed amniotes.

Conclusions:

  • The observed tail reduction mechanism suggests a potential commonality across amniote species.
  • Findings offer new insights into the developmental origins of the congenital 'human tail' anomaly.
  • Elucidating embryonic tail reduction is crucial for understanding human evolution and congenital anomalies.