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Updated: Mar 6, 2026

Organotypic Culture Method to Study the Development Of Embryonic Chicken Tissues
Published on: August 25, 2018
Primary hypoblast development in the chick : I. Scanning electron microscopy of normal development
Clement Weinberger1, Irving Brick2
1Department of Biology, Seton Hall University, 07079, South Orange, New Jersey, USA.
The primary hypoblast forms via epiblast cell downward movement (polyingression) and cell adhesion. This process, observed using scanning electron microscopy (SEM), establishes the early embryonic hypoblast layer.
Area of Science:
- Developmental biology
- Cell biology
- Embryology
Background:
- The early stages of embryonic development involve complex cellular rearrangements.
- Formation of the primary hypoblast is a critical early event in avian and mammalian embryogenesis.
Purpose of the Study:
- To investigate the cellular mechanisms and morphological changes during primary hypoblast formation.
- To utilize scanning electron microscopy (SEM) for detailed visualization of early embryonic surface topography.
Main Methods:
- Scanning electron microscopy (SEM) was employed to examine chick embryos during the first 8 hours of incubation.
- In situ fixation techniques were used to preserve delicate embryonic structures and minimize artifacts.
- Detailed morphological analysis of epiblast cell movement and hypoblast formation was performed.
Main Results:
- Primary hypoblast formation occurs beneath the area pellucida through polyingression of epiblast cells.
- Polyingression initiates posteriorly and progresses antero-laterally, creating surface pits and ridges.
- Epithelialization of the hypoblast involves cell adhesion, merging, and flattening, proceeding from posterior to anterior.
Conclusions:
- SEM provides high-resolution imaging of polyingression and hypoblast epithelialization.
- The study elucidates the dynamic cellular processes driving early hypoblast development.
- Cellular proliferation contributes to the cell population of the developing hypoblast.
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