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
. 1985 May;4(5):1163-70.
doi: 10.1002/j.1460-2075.1985.tb03755.x.

Do neurons in the vertebrate CNS migrate on laminin?

Do neurons in the vertebrate CNS migrate on laminin?

P Liesi. EMBO J. 1985 May.

Abstract

In adult rat brain the extracellular matrix glycoprotein, laminin, is found only in basement membranes, but is transiently expressed by astrocytes after brain injury. Here, I show that laminin also appears in immature brain cells during CNS development, and that its presence coincides with phases of neuronal migration. In early embryos, laminin is seen throughout the whole thickness of the forming brain, and is apparently synthesized by the cells, as judged by its intracytoplasmic localization. As development proceeds, intracellular laminin becomes restricted to the periventricular regions while punctate deposits of laminin follow the course of vimentin-positive radial glial fibers. In most brain regions, the adult pattern of laminin expression is achieved by birth. In the post-natal rat cerebellum, however, laminin is detected in external granule cells, in Purkinje cells, and in punctate deposits along the radial Bergmann glial fibers. By day 24 after birth, when the migration of external granule cells is complete, all laminin immunoreactivity disappears from these structures. The transient expression of laminin in regions where neurons are migrating raises the possibility that laminin plays a role in neuronal migration during CNS development.

PubMed Disclaimer

References

    1. EMBO J. 1984 Jan;3(1):1-10 - PubMed
    1. J Neurosci Res. 1982;8(2-3):179-93 - PubMed
    1. J Cell Biol. 1984 Mar;98(3):971-9 - PubMed
    1. J Cell Biol. 1978 Jul;78(1):176-98 - PubMed
    1. Proc Natl Acad Sci U S A. 1984 Jan;81(1):267-71 - PubMed

Publication types