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1.
Immunol Lett ; 138(1): 47-53, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21453726

ABSTRACT

The receptor activator of NF-κB ligand (RANKL), which is expressed by not only osteoblasts but also activated T cells, plays an important role in bone-destructive diseases such as rheumatoid arthritis. IL-27, a member of the IL-6/IL-12 family cytokines, activates STAT1 and STAT3, promotes early helper T (Th)1 differentiation and generation of IL-10-producing type 1 regulatory T (Tr1) cells, and suppresses the production of inflammatory cytokines and inhibits Th2 differentiation. In addition, IL-27 was recently demonstrated to not only inhibit Th17 differentiation but also directly act on osteoclast precursor cells and suppress RANKL-mediated osteoclastogenesis through STAT1-dependent inhibition of c-Fos, leading to amelioration of the inflammatory bone destruction. In the present study, we investigated the effect of IL-27 on the expression of RANKL in CD4(+) T cells. We found that IL-27 greatly inhibits cell surface expression of RANKL on naive CD4(+) T cells activated by T cell receptor ligation and secretion of its soluble RANKL as well. The inhibitory effect was mediated in part by STAT3 but not by STAT1 or IL-10. In contrast, in differentiated Th17 cells, IL-27 much less efficiently inhibited the RANKL expression after restimulation. Taken together, these results indicate that IL-27 greatly inhibits primary RANKL expression in CD4(+) T cells, which could contribute to the suppressive effects of IL-27 on the inflammatory bone destruction.


Subject(s)
CD4-Positive T-Lymphocytes/immunology , CD4-Positive T-Lymphocytes/metabolism , Gene Expression Regulation/drug effects , Interleukins/pharmacology , RANK Ligand/metabolism , STAT3 Transcription Factor/metabolism , Animals , CD4-Positive T-Lymphocytes/cytology , CD4-Positive T-Lymphocytes/drug effects , Cell Differentiation/drug effects , Cell Differentiation/immunology , Cells, Cultured , Lymphocyte Activation/immunology , Mice , Mice, Inbred C57BL , Receptors, Antigen, T-Cell/immunology , Receptors, Antigen, T-Cell/metabolism , STAT1 Transcription Factor/metabolism
2.
Protein Expr Purif ; 77(2): 193-7, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21296158

ABSTRACT

Cell-free protein synthesis systems are powerful tools for protein expression, and allow large amounts of specific proteins to be obtained even if these proteins are detrimental to cell survival. In this report we describe the effect of cysteine on cell-free protein synthesis. The addition of cysteine caused a 2.7-fold increase in the level of synthesized glutathione S-transferase (GST). Moreover, the levels of sulfhydryl group reductants, including reduced glutathione and dithiothreitol (DTT), were increased 1.9- and 1.7-fold, respectively, whereas levels of the disulfide dimers, cystine and oxidized glutathione, were suppressed 87% and 66%, respectively. These trends were also observed for green fluorescent protein (GFP) expression. The addition of cysteine competitively reversed the inhibitory effect of cystine on protein expression. These results suggest that the sulfhydryl group in cysteine plays a crucial role in enhancing protein synthesis, and that the addition of excess cysteine could be a convenient and useful method for improving protein expression.


Subject(s)
Cysteine/metabolism , Cystine/metabolism , Glutathione Transferase/biosynthesis , Green Fluorescent Proteins/biosynthesis , Protein Biosynthesis , Cell Fractionation , Cell-Free System , Chromatography, High Pressure Liquid , Disulfides/metabolism , Dithiothreitol/metabolism , Escherichia coli , Glutathione/metabolism , Glutathione Disulfide/metabolism , Glutathione Transferase/genetics , Green Fluorescent Proteins/genetics , RNA, Messenger/metabolism , Subcellular Fractions/chemistry , Subcellular Fractions/metabolism
3.
Life Sci ; 76(25): 2933-44, 2005 May 06.
Article in English | MEDLINE | ID: mdl-15820504

ABSTRACT

We previously reported for the first time that D-aspartate (D-Asp) is biosynthesized by cultured mammalian cells such as pheochromocytoma (PC)12 cells and its subclone MPT1 (FEBS Lett. 434 (1998) 231, Arch. Biochem. Biophys. 404 (2002) 92). We speculated that D-Asp levels in the intra- and extracellular spaces of the cultured cells are maintained in a dynamic state of homeostasis. To test this here, we utilized a novel and potent L-Glu transporter inhibitor, TFB-TBOA. This inhibitor proved to be a genuine nontransportable blocker of the transporter even during long periods of culture. Use of this inhibitor with MPT1 cells confirmed that D-Asp levels are in a dynamic steady state where it is constantly released into the extracellular space by a yet undefined mechanism as well as being constantly and intensively taken up by the cells via the L-Glu transporter. We estimated the rate with which D-Asp is constitutively released from MPT1 cells is approx. 3.8 pmol/h/1x10(5) cells.


Subject(s)
Amino Acid Transport System X-AG/antagonists & inhibitors , Aspartic Acid/pharmacology , D-Aspartic Acid/metabolism , Homeostasis/drug effects , Animals , Aspartic Acid/metabolism , Biological Transport/drug effects , Biological Transport/physiology , Chromatography, High Pressure Liquid , D-Aspartic Acid/physiology , Fluorescence , Homeostasis/physiology , PC12 Cells , Rats
4.
Arch Biochem Biophys ; 424(1): 89-96, 2004 Apr 01.
Article in English | MEDLINE | ID: mdl-15019840

ABSTRACT

In previous studies [FEBS Lett. 434 (1998) 231, Arch. Biochem. Biophys. 404 (2002) 92], we demonstrated for the first time that D-aspartate (D-Asp) is synthesized in cultured mammalian cell lines, such as pheochromocytoma 12 (PC12) and its subclone, MPT1. Our current focus is analysis of the dynamics of D-Asp homeostasis in these cells. In this communication, we show that L-glutamate (Glu) and L-Glu transporter substrates in the extracellular space regulate the homeostasis of endogenous D-Asp in MPT1 cells. D-Asp is apparently in dynamic homeostasis, whereby endogenous D-Asp is constantly released into the extracellular space by an undefined mechanism, and continuously and intensively taken up into cells by an L-Glu transporter. Under these conditions, L-Glu and its transporter substrates in the medium may competitively inhibit the uptake of D-Asp via the transporter, resulting in accumulation of the amino acid in the extracellular space. We additionally demonstrate that DL-TBOA, a well-established L-Glu transporter inhibitor, is taken up by the transporter during long time intervals, but not on a short time-scale.


Subject(s)
Aspartic Acid/metabolism , Cysteine/analogs & derivatives , Glutamic Acid/metabolism , Amino Acid Transport System X-AG/antagonists & inhibitors , Amino Acid Transport System X-AG/metabolism , Animals , Aspartic Acid/analogs & derivatives , Aspartic Acid/pharmacology , Cell Line, Tumor , Cysteine/metabolism , Cysteine/pharmacology , Extracellular Space/metabolism , Glutamic Acid/pharmacology , Homeostasis , Neurotransmitter Agents , PC12 Cells , Pheochromocytoma/metabolism , Rats
5.
Anal Sci ; 19(9): 1281-4, 2003 Sep.
Article in English | MEDLINE | ID: mdl-14516080

ABSTRACT

It has previously been pointed out that two different mechanisms exist in the reversed-phase (RP) HPLC of polypeptides, including proteins. We systematically investigated the separation of various peptides and proteins over a wide range of molecular weight using a nonporous octadecylsilyl (ODS) silica-gel column to provide a precise explanation for the separation mechanism of polypeptides, including proteins in RP-HPLC. As a result, we clarified that a critical point between a typical reversed-phase partition mode applicable to small peptides (molecular weight < 3000) and a characteristic elution mode applicable to proteins is in the vicinity of the molecular weight of 3500-4500. We also proposed a new concept, the "Transitional Desorption Mode", as a separation mechanism that can precisely explain the RP-LC separation of a wide range of polypeptides including proteins.


Subject(s)
Peptides/isolation & purification , Proteins/isolation & purification , Chromatography, High Pressure Liquid , Models, Chemical , Molecular Weight , Silica Gel , Silicon Dioxide/chemistry
6.
Anal Biochem ; 315(2): 262-9, 2003 Apr 15.
Article in English | MEDLINE | ID: mdl-12689836

ABSTRACT

A novel optically active thiol compound, N-(tert-butylthiocarbamoyl)-L-cysteine ethyl ester (BTCC), is synthesized as a chiral derivatization reagent. This compound and o-phthalaldehyde react with amino acid enantiomers to produce fluorescent diastereomers that are readily separable on a reverse-phase column by HPLC. Enantioseparation of acidic amino acids in particular is markedly improved using BTCC. In this study, the HPLC method for enantioseparation with the novel compound is applied to the aspartate (Asp) racemase assay. Derivatized D-Asp is eluted before the L-Asp derivative. Consequently, a small amount of D-Asp produced by the activity of racemase on a large quantity of L-Asp substrate may be quantified accurately, even at very low activity. Since the derivatization reaction proceeds rapidly at room temperature, a fully automated system is established for derivatization and sample injection. The automated method is practical and successfully applied to the archaeal Asp racemase assay. We presume that the procedure is additionally applicable to the enantioseparation of other amino acids, amino alcohols, and catecholamines.


Subject(s)
Amino Acid Isomerases/metabolism , Amino Acids/isolation & purification , Chromatography, High Pressure Liquid/methods , Sulfhydryl Reagents/chemistry , Amino Acid Isomerases/analysis , Amino Acids/analysis , Amino Acids/chemistry , Automation , Calibration , Molecular Structure , Stereoisomerism , Sulfhydryl Reagents/chemical synthesis
7.
Anal Biochem ; 310(1): 114-21, 2002 Nov 01.
Article in English | MEDLINE | ID: mdl-12413481

ABSTRACT

The occurrence and biological significance of the D-amino acids, N-methyl-D-aspartate (NMDA) and N-methyl-L-aspartate (NMLA), have been recently studied in a variety of living organisms. In this study, we established a highly sensitive and reliable fluorometric HPLC system for determining levels of N-methyl-aspartate (NMA). The system comprises fluorescent derivatization of NMA with 4-fluoro-7-nitro-2,1,3-benzoxadiazole (NBD-F) and two chromatographic steps: one that separates NMA from other primary amino acids in reverse-phase mode and another that enantioseparates NMDA and NMLA in a normal-phase mode. These two steps are linked by an automated column-switching system. A simple pretreatment step with o-phthalaldehyde to remove primary amino acids that can interfere with sensitivity is also described. The detection limit for NMDA is as low as 5fmol and the correlation between peak heights and concentrations between 5fmol and 1pmol is satisfactory (r=0.999). Following sample preparation and separation using the column-switching HPLC system, more than 80% of NMDA was recovered from rat liver homogenates spiked with NMDA. This method was employed to determine the levels of NMDA in tissues from bivalves and the results obtained were consistent with the values reported previously.


Subject(s)
4-Chloro-7-nitrobenzofurazan/analogs & derivatives , Chromatography, High Pressure Liquid/methods , N-Methylaspartate/analysis , 4-Chloro-7-nitrobenzofurazan/chemistry , Acetonitriles/chemistry , Amino Acids/chemistry , Animals , Automation , Bivalvia/chemistry , Chromatography, High Pressure Liquid/instrumentation , Fluorescence , N-Methylaspartate/chemistry , Reproducibility of Results , Sensitivity and Specificity , Stereoisomerism , o-Phthalaldehyde/chemistry
8.
Arch Biochem Biophys ; 404(1): 92-7, 2002 Aug 01.
Article in English | MEDLINE | ID: mdl-12127073

ABSTRACT

In a previous report (FEBS Lett. 434 (1998) 231), we demonstrated for the first time that D-aspartate (D-Asp) is synthesized in rat pheochromocytoma 12 (PC12) cells. This unique amino acid is believed to act as a novel messenger in mammalian cell regulation. However, the dynamics of D-Asp homeostasis in mammalian cells is yet to be elucidated. In this communication, we demonstrate that D-Asp is also synthesized in MPT1 cells (a subclone of PC12 cells) and that the D- and L-Asp levels in cells are regulated by cell density of the culture. Our data show that D-Asp levels increase, while in contrast, L-Asp levels decrease as a function of increased cell density. Conversely, in PC12 cells, which do not express the glutamate transporter involved in the incorporation of D- and L-Asp into cells, L-Asp levels decrease upon cell density increase while D-Asp concentrations remain almost unchanged. The results indicate that the biochemical behaviors of D- and L-Asp in mammalian cells are distinct and that the cellular levels of these stereoisomers appear to be under different control mechanisms.


Subject(s)
Aspartic Acid/metabolism , Pheochromocytoma/metabolism , Animals , Aspartic Acid/biosynthesis , Aspartic Acid/chemistry , Cell Count , Homeostasis , PC12 Cells , Pheochromocytoma/pathology , Rats , Stereoisomerism
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