Data di Pubblicazione:
2009
Abstract:
The Lgi1 protein is involved in the pathogenesis
of autosomal dominant lateral temporal epilepsy
because mutations in the leucine-rich, glioma-inactivated 1
(LGI1) gene have been found in aVected subjects and
families; however, the function of Lgi1 is still unclear.
DeWnition of the Wne intracellular distribution of Lgi1 in
normal cortical tissue would add in understanding its role
and envisage pathogenetic mechanisms. Therefore, we
analyzed normal rat cortex for Lgi1 by combining biochemistry,
immunohistochemistry and immunoelectron
microscopy. Our results demonstrate that Lgi1 is a cytoplasmic
protein distributed both in the soma and in the processes
of neurons: it occurs on the rough endoplasmic
reticulum, the site of synthesis, in the Golgi complex,
where it undergoes glycosylation, and in close proximity to
neurotubules and neuroWlaments, especially in the axons,
but it is scarce at synapses and the neurilemma. Lgi1 association
with axonal cytoskeletal structures would imply
Lgi1 is either transported along axons by motor proteins, or
playing some role as a carrier in the axonal Xux, or it could
be involved in the regulation of cytoskeletal organization.
Tipologia CRIS:
01.01 Articolo in rivista
Elenco autori:
Furlan, Sandra; Nobile, Carlo
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