Journal
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
Volume 294, Issue 4, Pages C1012-C1020Publisher
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpcell.00411.2007
Keywords
S-nitrosothiols; cysteine; cystine; amino acid transporters
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Funding
- NHLBI NIH HHS [HL-42444, HL-61377] Funding Source: Medline
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We have shown previously that extracellular cysteine is necessary for cellular responses to S- nitrosoalbumin. In this study we have investigated mechanisms involved in accumulation of extracellular cysteine outside vascular smooth muscle cells and characterized the role of cystine- cysteine release in transfer of nitric oxide (NO)- bioactivity. Incubation of cells with cystine led to cystine uptake, reduction, and cysteine release. The process was inhibitable by extracellular glutamate, suggesting a role for system x(c)(-) amino acid transporters. Smooth muscle cells express this transporter constitutively and induction of the light chain component (xCT) by either diethyl maleate or 3- morpholinosydnonimine (SIN- 1) led to glutamate- inhibitable cystine uptake and an increased rate of cysteine release from cells. Likewise, overexpression of xCT in smooth muscle cells or endothelial cells led to glutamate- inhibitable cysteine release. The resulting extracellular cysteine was found to be required for transfer of NO from extracellular S- nitrosothiols into cells via system L transporters leading to formation of cellular S- nitrosothiols. Cysteine release coupled to cystine uptake was also found to be required for cellular responses to S- nitrosoalbumin and facilitated S- nitrosoalbumin- mediated inhibition of epidermal growth factor signaling. These data show that xCT expression can constitute a cystine- cysteine shuttle whereby cystine uptake drives cysteine release. Furthermore, we show that extracellular cysteine provided by this shuttle mechanism is necessary for transfer of NO equivalents and cellular responses to S- nitrosoablumin.
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