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Cancer Cell death Cell cycle Cytoskeleton Exo/endocytosis Differentiation Division Organelles Signalling Stem cells Trafficking
Cell Biology International (2010) 34, 27–33 (Printed in Great Britain)
Proteomic analysis to identify early molecular targets of pregabalin in C6 glial cells
Seyeon Park*1 and Joomin Lee†
*Department of Applied Chemistry, Dongduk Women's University, Seoul 136-714, Korea, and †Department of Food and Nutrition, Yonsei University, Seoul 134, Korea

Pregabalin is a lipophilic amino acid derivative of γ-amino butyric acid that displays anticonvulsant and analgesic activities against neuropathic pain. Although a role for glial cells as an important player in pain control and also as a new target for pain medicine has been suggested, the effect of pregabalin on glial cells has not been elucidated. In the present study, we have investigated the action of pregabalin on the glial cell proteome. To identify immediate early protein targets of pregabalin in glial cells, a differential proteomics approach in C6 rat glioma cells treated with pregabalin was used. Seven proteins that sensitively reacted to pregabalin treatment were identified using two-dimensional gel electrophoresis and MALDI–TOF-MS (matrix-assisted laser-desorption ionization–time-of-flight MS). The calcium-ion-binding chaperone, calreticulin, and the oxidative response protein, DJ-1, were up-regulated after pregabalin treatment. Hsp (heat-shock protein)-90-β, cytoskeleton protein actin and myosin also showed quantitative expression profile differences. Functionally relevant to the proteome result, immediate actin depolymerization was observed after treatment with pregabalin. These results suggest a previously undefined role of pregabalin in the regulation of chaperone activity and cytoskeleton remodelling in glial cells.

Key words: C6 glial cell, calreticulin, cytoskeleton, DJ-1, pregabalin, proteomic approach

Abbreviations: Epac, exchange protein directly activated by cAMP, GABA, γ-amino butyric acid, GAPDH, glyceraldehyde-3-phosphate dehydrogenase, Hsp, heat-shock protein, MALDI–TOF-MS, matrix-assisted laser-desorption ionization–time-of-flight MS, PBST, PBS containing 0.1% Tween 20

1To whom correspondence should be addressed (email

Received 8 May 2009/11 June 2009; accepted 7 September 2009

Published as Cell Biology International Immediate Publication 7 September 2009, doi:10.1042/CBI20090018

© 2010 The Author(s) Journal compilation. © 2010 Portland Press Ltd

ISSN Print: 1065-6995
ISSN Electronic: 1095-8355
Published by Portland Press Limited on behalf of the International Federation for Cell Biology (IFCB)