Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014 Aug 28;55(4):299-305.
doi: 10.3325/cmj.2014.55.299.

Embryonic cerebrospinal fluid in brain development: neural progenitor control

Affiliations
Review

Embryonic cerebrospinal fluid in brain development: neural progenitor control

Angel Gato et al. Croat Med J. .

Abstract

Due to the effort of several research teams across the world, today we have a solid base of knowledge on the liquid contained in the brain cavities, its composition, and biological roles. Although the cerebrospinal fluid (CSF) is among the most relevant parts of the central nervous system from the physiological point of view, it seems that it is not a permanent and stable entity because its composition and biological properties evolve across life. So, we can talk about different CSFs during the vertebrate life span. In this review, we focus on the CSF in an interesting period, early in vertebrate development before the formation of the choroid plexus. This specific entity is called "embryonic CSF." Based on the structure of the compartment, CSF composition, origin and circulation, and its interaction with neuroepithelial precursor cells (the target cells) we can conclude that embryonic CSF is different from the CSF in later developmental stages and from the adult CSF. This article presents arguments that support the singularity of the embryonic CSF, mainly focusing on its influence on neural precursor behavior during development and in adult life.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Development of the mouse embryo after 10.5 days. (A) Transversal histological hematoxilin-eosin stained section. (B) Macroscopic view showing the neural tube by transilumination.

References

    1. Gato A, Desmond ME. Why the embryo still matters: CSF and the neuroepithelium as interdependent regulators of embryonic brain growth, morphogenesis and histiogenesis. Dev Biol. 2009;327:263–72. doi: 10.1016/j.ydbio.2008.12.029. - DOI - PubMed
    1. Pai YJ, Abdullah NL, Mohd-Zin SW, Mohammed RS, Rolo A, Greene ND, et al. Epithelial fusion during neural tube morphogenesis. Birth Defects Res A Clin Mol Teratol. 2012;94:817–23. doi: 10.1002/bdra.23072. - DOI - PMC - PubMed
    1. Yamaguchi Y, Miura M. How to form and close the brain: insight into the mechanism of cranial neural tube closure in mammals. Cell Mol Life Sci. 2013;70:3171–86. doi: 10.1007/s00018-012-1227-7. - DOI - PMC - PubMed
    1. Desmond ME, Schoenwolf GC. Timing and positioning of occlusion of the spinal neurocele in the chick embryo. J Comp Neurol. 1985;235:479–87. doi: 10.1002/cne.902350406. - DOI - PubMed
    1. Desmond ME, Levitan ML. Brain expansion in the chick embryo initiated by experimentally produced occlusion of the spinal neurocoel. Anat Rec. 2002;268:147–59. doi: 10.1002/ar.10146. - DOI - PubMed

Publication types