Characterization of human thioredoxin-like-1: potential involvement in the cellular response against glucose deprivation |
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Authors: | Jiménez Alberto Pelto-Huikko Markku Gustafsson Jan-Ake Miranda-Vizuete Antonio |
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Affiliation: | Center for Biotechnology, Department of Biosciences at NOVUM, Karolinska Institutet, S-14157 Huddinge, Sweden. |
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Abstract: | The thioredoxin system, composed of thioredoxin (Trx) and thioredoxin reductase (TrxR), emerges as one of the most important thiol-based systems involved in the maintenance of the cellular redox balance. Thioredoxin-like-1 (TXL-1) is a highly conserved protein comprising an N-terminal Trx domain and a C-terminal domain of unknown function. Here we show that TXL-1 is a substrate for the cytosolic selenoprotein TrxR-1. In situ hybridization experiments demonstrates high expression of Txl-1 mRNA in various areas of central nervous system and also in some reproductive organs. Glucose deprivation, but not hydrogen peroxide treatment, reduced the levels of endogenous TXL-1 protein in HEK-293 cell line. Conversely, overexpression of TXL-1 protects against glucose deprivation-induced cytotoxicity. Taken together, the finding that Txl-1 mRNA is highly expressed in tissues which use glucose as a primary energy source and the modulation of TXL-1 levels upon glucose deprivation indicate that TXL-1 might be involved in the cellular response to sugar starvation stress. |
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Keywords: | DTT, dithiothretitol GST, glutathione-S-transferase MTT, 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide Trx, thioredoxin TrxR, thioredoxin reductase Txl, thioredoxin-like HEK, human embryonic kidney |
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