Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2012 Aug;46(2):246-56.
doi: 10.1002/mus.23306.

Proteomic Analysis in Giant Axonal Neuropathy: New Insights Into Disease Mechanisms

Affiliations

Proteomic Analysis in Giant Axonal Neuropathy: New Insights Into Disease Mechanisms

Silke Mussche et al. Muscle Nerve. .

Abstract

Introduction: Giant axonal neuropathy (GAN) is a progressive hereditary disease that affects the peripheral and central nervous systems. It is characterized morphologically by aggregates of intermediate filaments in different tissues. Mutations have been reported in the gene that codes for gigaxonin. Nevertheless, the underlying molecular mechanism remains obscure.

Methods: Cell lines from 4 GAN patients and 4 controls were analyzed by iTRAQ.

Results: Among the dysregulated proteins were ribosomal protein L29, ribosomal protein L37, galectin-1, glia-derived nexin, and aminopeptidase N. Also, nuclear proteins linked to formin-binding proteins were found to be dysregulated. Although the major role of gigaxonin is reported to be degradation of cytoskeleton-associated proteins, the amount of 76 structural cytoskeletal proteins was unaltered.

Conclusions: Several of the dysregulated proteins play a role in cytoskeletal reorganization. Based on these findings, we speculate that disturbed cytoskeletal regulation is responsible for formation of aggregates of intermediate filaments.

Similar articles

See all similar articles

Cited by 3 articles

Publication types

LinkOut - more resources

Feedback