Kobayashi Sho, Sato Mami, Kasakoshi Takayuki, Tsutsui Takumi, Sugimoto Masahiro, Osaki Mitsuhiko, Okada Futoshi, Igarashi Kiharu, Hiratake Jun, Homma Takujiro, Conrad Marcus, Fujii Junichi, Soga Tomoyoshi, Bannai Shiro, Sato Hideyo
From the Department of Food and Applied Life Sciences, Faculty of Agriculture, Yamagata University, Tsuruoka, Yamagata 997-8555, Japan, the Department of Functional Genomics and Biotechnology, United Graduate School of Agricultural Sciences, Iwate University, Morioka, Iwate 020-8550, Japan, the Helmholtz Center Munich, German Research Center for Environmental Health, Institute of Developmental Genetics, Ingolstädter Landstrasse 1, 85764 Neuherberg, Germany.
From the Department of Food and Applied Life Sciences, Faculty of Agriculture, Yamagata University, Tsuruoka, Yamagata 997-8555, Japan.
J Biol Chem. 2015 Apr 3;290(14):8778-88. doi: 10.1074/jbc.M114.625053. Epub 2015 Feb 20.
The cystine/glutamate transporter, designated as system xc(-), is important for maintaining intracellular glutathione levels and extracellular redox balance. The substrate-specific component of system xc(-), xCT, is strongly induced by various stimuli, including oxidative stress, whereas it is constitutively expressed only in specific brain regions and immune tissues, such as the thymus and spleen. Although cystine and glutamate are the well established substrates of system xc(-) and the knockout of xCT leads to alterations of extracellular redox balance, nothing is known about other potential substrates. We thus performed a comparative metabolite analysis of tissues from xCT-deficient and wild-type mice using capillary electrophoresis time-of-flight mass spectrometry. Although most of the analyzed metabolites did not show significant alterations between xCT-deficient and wild-type mice, cystathionine emerged as being absent specifically in the thymus and spleen of xCT-deficient mice. No expression of either cystathionine β-synthase or cystathionine γ-lyase was observed in the thymus and spleen of mice. In embryonic fibroblasts derived from wild-type embryos, cystine uptake was significantly inhibited by cystathionine in a concentration-dependent manner. Wild-type cells showed an intracellular accumulation of cystathionine when incubated in cystathionine-containing buffer, which concomitantly stimulated an increased release of glutamate into the extracellular space. By contrast, none of these effects could be observed in xCT-deficient cells. Remarkably, unlike knock-out cells, wild-type cells could be rescued from cystine deprivation-induced cell death by cystathionine supplementation. We thus conclude that cystathionine is a novel physiological substrate of system xc(-) and that the accumulation of cystathionine in immune tissues is exclusively mediated by system xc(-).
胱氨酸/谷氨酸转运体,被命名为系统xc(-),对于维持细胞内谷胱甘肽水平和细胞外氧化还原平衡至关重要。系统xc(-)的底物特异性成分xCT,受到包括氧化应激在内的各种刺激的强烈诱导,而它仅在特定脑区和免疫组织(如胸腺和脾脏)中组成性表达。尽管胱氨酸和谷氨酸是系统xc(-)公认的底物,且xCT基因敲除会导致细胞外氧化还原平衡改变,但对于其他潜在底物却一无所知。因此,我们使用毛细管电泳飞行时间质谱法对xCT基因缺陷小鼠和野生型小鼠的组织进行了比较代谢物分析。尽管大多数分析的代谢物在xCT基因缺陷小鼠和野生型小鼠之间没有显示出显著变化,但胱硫醚却特别在xCT基因缺陷小鼠的胸腺和脾脏中缺失。在小鼠的胸腺和脾脏中未观察到胱硫醚β-合酶或胱硫醚γ-裂合酶的表达。在源自野生型胚胎的胚胎成纤维细胞中,胱硫醚以浓度依赖的方式显著抑制胱氨酸摄取。野生型细胞在含胱硫醚的缓冲液中孵育时会出现细胞内胱硫醚积累,这同时刺激了谷氨酸向细胞外空间释放增加。相比之下,在xCT基因缺陷细胞中未观察到这些效应。值得注意的是,与基因敲除细胞不同,补充胱硫醚可使野生型细胞从胱氨酸剥夺诱导的细胞死亡中获救。因此,我们得出结论,胱硫醚是系统xc(-)的一种新型生理底物,且免疫组织中胱硫醚的积累完全由系统xc(-)介导。