Human cystine/glutamate transporter: cDNA cloning and upregulation by oxidative stress in glioma cells

Citation
Jy. Kim et al., Human cystine/glutamate transporter: cDNA cloning and upregulation by oxidative stress in glioma cells, BBA-BIOMEMB, 1512(2), 2001, pp. 335-344
Citations number
34
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES
ISSN journal
00052736 → ACNP
Volume
1512
Issue
2
Year of publication
2001
Pages
335 - 344
Database
ISI
SICI code
0005-2736(20010606)1512:2<335:HCTCCA>2.0.ZU;2-B
Abstract
A human cDNA for amino acid transport system x(C)(-) was isolated from diet hyl maleate-treated human glioma U87 cells. u87 cells expressed two variant s of system x(C)(-) transporters hxCTa and hxCTb with altered C-terminus re gions probably generated by the alternative splicing at 3'-ends. Both hxCTa and hxCTb messages were also detected in spinal cord, brain and pancreas, although the level of hxCTb expression appears to be lower than that of hxC Ta in these tissues. When expressed in Xenopus oocytes, hxCTb required the heavy chain of 4F2 cell surface antigen (4F2hc) and exhibited the Na+-indep endent transport of L-cystine and L-glutamate, consistent with the properti es of system x(C)(-). In agreement with this, 137 kDa band was detected by either anti-xCT or anti-4F2hc antibodies in the non-reducing condition in w estern blots, whereas it shifted to 50 kDa or 90 kDa bands in the reducing condition, indicating the association of two proteins via disulfide bands. We found that the expression of xCT was rapidly induced in U87 cells upon o xidative stress by diethyl maleate treatment, which was accompanied by the increase in the L-cystine uptake by U87 cells. Because of this highly regul ated nature, xCT in glial cells would fulfill the task to protect neurons a gainst oxidative stress by providing suitable amount of cystine to produce glutathione. (C) 2001 Elsevier Science B.V. All rights reserved.