Expression of nogo-a is decreased with increasing gestational age in the human fetal brain.

Abstract:

:Nogo is a member of the reticulon family. Our understanding of the physiological functions of the Nogo-A protein has grown over the last few years, and this molecule is now recognized as one of the most important axonal regrowth inhibitors present in central nervous system (CNS) myelin. Nogo-A plays other important roles in nervous system development, epilepsy, vascular physiology, muscle pathology, stroke, inflammation, and CNS tumors. Since the exact role of Nogo-A protein in human brain development is still poorly understood, we studied its cellular and regional distribution by immunohistochemistry in the frontal lobe of 30 human fetal brains. Nogo-A was expressed in the following cortical zones: ependyma, ventricular zone, subventricular zone, intermediate zone, subplate, cortical plate, and marginal zone. The number of positive cells decreased significantly with increasing gestational age in the subplate and marginal zone. Using different antibodies, changes in isoform expression and dimerization states could be shown between various cortical zones. The results demonstrate a significant change in the expression of Nogo-A during the development of the human brain. The effects of its time- and region-specific regulation have to be further studied in detail.

journal_name

Dev Neurosci

authors

Haybaeck J,Llenos IC,Dulay RJ,Bettermann K,Miller CL,Wälchli T,Frei K,Virgintino D,Rizzi M,Weis S

doi

10.1159/000343143

subject

Has Abstract

pub_date

2012-01-01 00:00:00

pages

402-16

issue

5

eissn

0378-5866

issn

1421-9859

pii

000343143

journal_volume

34

pub_type

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