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Updated: Aug 16, 2026

Neural Tube Closure in Mouse Whole Embryo Culture
Published on: October 21, 2011
Teratogenic effects of retinoic acid on neurulation in mice embryos
M Nobakht1, A Zirak, M Mehdizadeh
1Department of Anatomy and Histology, Iran University Of Medical Sciences, P.O. Box 14155-6183, Tehran, Iran. nobakht@yahoo.com
Abstract:
Retinoic acids (RA) are natural chemicals that exert a hormone-like activity and a variety of biological effects on early development of mouse. In this study, the probable teratogenic effects of RA on CNS have been investigated in pregnant mice (n = 20) divided into four groups: (1) untreated controls, (2) controls which received a single dose of DMSO, (3) a group that received 40 mg/kg, and (4) a group that received 60 mg/kg of all-trans RA in DMSO, respectively on the eighth day of gestation. Embryos whose dams had received 40 and 60 mg/kg doses of RA, showed malformations and decreased size. At 40 mg/kg dosage level, 50% of the embryos had closed neural tubes while at 60 mg/kg dosage level the neural tube failed to close. The neuroblast mantle layers were disorganized in the 40 mg/kg and even more in the 60 mg/kg exposed group compared to the controls. In mitosis, the density of chromatin was increased in the 60 mg/kg dose group. Compared to controls the 40 and 60 mg/kg dose groups of RA treated dams decreases in the luminal longitudinal and internal measures were observed. Also the thickness of ventricular, mantle and marginal layers was smaller. Wide intercellular spaces due to the degenerated cells at high doses of RA as well as an accumulation of intercellular fluid were observed. Therefore, the wedge shape of neuroepithelium was abolished, preventing the elevation of the neural wall.
Insights
High doses of all-trans retinoic acid (RA) cause significant birth defects in mouse embryos, particularly affecting central nervous system (CNS) development. RA exposure disrupted neural tube closure and disorganized developing brain structures.
Area of Science:
- Developmental Biology
- Neuroscience
- Toxicology
Background:
- Retinoic acids (RA) are crucial signaling molecules regulating embryonic development.
- Aberrant RA signaling is implicated in various congenital malformations.
Purpose of the Study:
- To investigate the teratogenic effects of all-trans retinoic acid (RA) on the developing central nervous system (CNS) in mouse embryos.
- To determine dose-dependent effects of RA on neural tube closure and neuroepithelial organization.
Main Methods:
- Pregnant mice were administered varying doses of all-trans RA (40 and 60 mg/kg) or vehicle (DMSO) on day 8 of gestation.
- Embryos were examined for malformations, size, neural tube closure, and histological changes in CNS layers.
Main Results:
- RA exposure led to embryo malformations and reduced size.
- Significant dose-dependent inhibition of neural tube closure was observed (50% closure at 40 mg/kg, failure at 60 mg/kg).
- Histological analysis revealed disorganized neuroblast layers, increased chromatin density, reduced layer thickness, intercellular spaces, and fluid accumulation.
Conclusions:
- All-trans retinoic acid exhibits potent teratogenic effects on the developing CNS in mice.
- RA disrupts critical developmental processes including neural tube formation and neuroepithelial structure.
- These findings highlight the sensitivity of early embryonic development to retinoic acid signaling.
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Teratogenicity
Neurulation