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Oxidative modifications of cerebral transthyretin are associated with multiple sclerosis

Authors :
Diego Franciotta
Maria di Ioia
Andrea Urbani
Piero Del Boccio
Luisa Pieroni
Damiana Pieragostino
Diego Centonze
Giovanna De Luca
Alessandra Lugaresi
Claudia Rossi
Simona D'Aguanno
Carmine Di Ilio
Paolo Sacchetta
V. Greco
Pieragostino Damiana
Del Boccio Piero
Di Ioia Maria
Pieroni Luisa
Greco Viviana
De Luca Giovanna
D'Aguanno Simona
Rossi Claudia
Franciotta Diego
Centonze Diego
Sacchetta Paolo
Di Ilio Carmine
Lugaresi Alessandra
Urbani Andrea
Source :
Proteomics. 13(6)
Publication Year :
2012

Abstract

Transthyretin (TTR) is a homotetrameric protein of the CNS that plays a role of as the major thyroxine (T4) carrier from blood to cerebrospinal fluid (CSF). T4 physiologically helps oligodendrocyte precursor cells to turn into myelinating oligodendrocytes, enhancing remyelination after myelin sheet damage. We investigated post-translational oxidative modifications of serum and CSF TTR in multiple sclerosis subjects, highlighting high levels of S-sulfhydration and S-sulfonation of cysteine in position ten only in the cerebral TTR, which correlate with an anomalous TTR protein folding as well as with disease duration. Moreover, we found low levels of free T4 in CSF of multiple sclerosis patients, suggestive of a potential role of these modifications in T4 transport into the brain.

Details

ISSN :
16159861
Volume :
13
Issue :
6
Database :
OpenAIRE
Journal :
Proteomics
Accession number :
edsair.doi.dedup.....80ee85ff907d18a37791c3921d9b8429