S-Nitrosation of cellular proteins by no donors in rat embryonic fibroblast 3Y1 cells: Factors affecting S-nitrosation

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Abstract

The mechanism of protein S-nitrosation in cells is not fully understood. Using rat 3Y1 cells, we addressed this issue. Among S-nitrosothiols and NO donors tested, only S-nitrosocysteine (CysNO) induced S-nitrosation when exposed in Hanks' balanced salt solution (HBSS) and not in serum-containing general culture medium. In HBSS, NO release from CysNO was almost completely abolished by sequestering metal ions with a metal chelator without affecting cellular S-nitrosation. In contrast, L-leucine, a substrate of L-type amino acid transporters (LATs), significantly inhibited S-nitrosation. The absence of S-nitrosation with CysNO in general culture medium resulted not only from a competition with amino acids in the medium for LATs but also from transnitrosation of cysteine residues in serum albumin. Collectively, these results suggest that in simple buffered saline, CysNO-dependent S-nitrosation occurs through a cellular incorporation-dependent mechanism, but if it occurs in general culture media, it may be through an NO-dependent mechanism. © 2011 Norihiro Ryuman et al.

Figures

  • Figure 1: Protein S-nitrosation induced by potential S-nitrosating agents in 3Y1 cell lysates. (a) Detection of S-nitrosated proteins in cell lysate treated with potential S-nitrosating agents. 3Y1 cell lysates prepared in PBS containing 0.5mM EDTA and 0.5% Triton X-100 were incubated with CysNO (200 μM), GSNO (200μM), NOR-3 (200 μM), or SIN-1 (1mM) at 37◦C for 30min. S-nitrosated proteins were detected by the biotin-switch assay. (b) Specificity of the biotin switch assay. 3Y1 cells lysates were incubated with or withoutGSNO (500μM), and the resulting S-nitrosated proteins were assessed by biotin-switch assay as above, but with or without ascorbate in the biotinylation step. A 10% gel was used for this confirmation experiment. Therefore, the resolution of S-nitrosated protein bands was different from that in all other experiments in which 6.0%–16.5% gradient gels were used.
  • Figure 2: Protein S-nitrosation induced by exposure to potential S-nitrosating agents in intact 3Y1 cells. (a) Comparison of the efficiencies of potential S-nitrosating agents to S-nitrosate 3Y1 cells. Cells maintained in HBSS were treated with CysNO (200μM), GSNO (200μM), NOR-3 (200 μM), or SIN-1 (1mM) for 30min. S-nitrosated proteins were detected by the biotin-switch assay. (b and c) Effects of media on S-nitrosation efficiency of S-nitrosothiols. Cells cultured in 10% FCS/DMEM andHBSS were treated with GSNO (1mM) or CysNO (1mM) for 30min, and S-nitrosated proteins were detected by (b) the biotin-switch assay and (c) the DAN assay. The blots shown in (a) and (b) are representative results from several experiments with similar results. Data in (c) are shown as mean ± SEM of three to four independent assays.
  • Figure 3: Effects of DETAPAC, DTNB, and L-leucine on CysNO-induced S-nitrosation in 3Y1 cells. (a) NO release from S-nitrosothiols in HBSS. CysNO or GSNO was diluted in HBSS to a final concentration of 200 μM without or with DETAPAC (0.5 mM). NO concentration in the medium was aerobically monitored at 37◦C using an NO electrode. The trace shown is a representative result. (b and c) Effects of DETAPAC, DTNB, and L-leucine on CysNO-induced S-nitrosation in 3Y1 cells. Cells in HBSS were treated with CysNO (200 μM) for 30 min in the absence or presence of DETAPAC (0.5mM), L-leucine (1mM), and DTNB (100 μM), which were added 20min before the addition of CysNO. Protein S-nitrosation was detected using (b) the DAN assay and (c) the biotin-switch assay. The blot shown is a representative result. (d) The efficiency of CysNO- and D-CysNO-induced S-nitrosation, each at 200 μM, was measured by the DAN assay as in (b). S-nitrosothiol levels in cells treated with CysNO alone (labeled “none” in (b)) were taken as 100% (12 ± 2 nmol SNO/mg protein), and the values are expressed as the mean ± SEM of six to eight independent experiments in (b) and from three independent experiments in (d). ∗P < 0.001.
  • Figure 4: Effects of FCS, BSA, and NEM-BSA on CysNO-mediated S-nitrosation in 3Y1 cells. Cells maintained in HBSS or DMEM in the absence or presence of FCS (10%), BSA (3mg/ml), or NEMtreated BSA (3mg/ml) were treated with CysNO (200μM) for 30min. The levels of S-nitrosated proteins were measured by the DAN assay, and the value for cells treated with CysNO in HBSS alone (none) was taken as 100% (12 ± 2 nmol/mg protein). Values are mean ± SEM of three to four independent assays. ∗P < 0.001 versus none; #P < 0.001 versus BSA.

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Watanabe, N., Ryuman, N., & Arai, T. (2011). S-Nitrosation of cellular proteins by no donors in rat embryonic fibroblast 3Y1 cells: Factors affecting S-nitrosation. Oxidative Medicine and Cellular Longevity. https://doi.org/10.1155/2011/450317

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