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1.
We investigated whether or not the inflammatory cytokines affect the activity of taurine transporter (TAUT) in human intestinal Caco-2 cells. Among the cytokines, tumor necrosis factor alpha(TNF-alpha) markedly augmented the TAUT activity. A kinetic analysis of the TAUT activity in TNF-alpha-treated Caco-2 cells suggests that this up-regulation was associated with both an increase in the amount of TAUT and an increase in its affinity. Considering these results, it seems that intracellular taurine plays a role in the intestinal epithelial cells under such an inflammatory condition as that caused by an excessive amount of TNF-alpha secreted by macrophages. To verify this hypothesis, we examined the effect of taurine on inflamed intestinal cells by using a co-culture system of Caco-2 cells with human macrophage-like THP-1 cells. The result shows that taurine significantly repressed the damage to Caco-2 cells caused by TNF-alpha secreted by THP-1 cells. Thus, taurine may be a useful substance against intestinal inflammation. 相似文献
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Summary. This paper examines a unique hypothesis regarding an important role for taurine in renal development. Taurine-deficient neonatal
kittens show renal developmental abnormalities, one of several lines of support for this speculation. Adaptive regulation
of the taurine transporter gene is critical in mammalian species because maintenance of adequate tissue levels of taurine
is essential to the normal development of the retina and the central nervous system. Observations of the remarkable phenotypic
similarity that exists between children with deletion of bands p25-pter of chromosome 3 and taurine-deficient kits led us
to hypothesize that deletion of the renal taurine transporter gene (TauT) might contribute to some features of the 3p-syndrome.
Further, the renal taurine transporter gene is down-regulated by the tumor suppressor gene p53, and up-regulated by the Wilms
tumor (WT-1) and early growth response-1 (EGR-1) genes. It has been demonstrated using WT-1 gene knockout mice that WT-1 is
critical for normal renal development. In contrast, transgenic mice overexpressing the p53 gene have renal development defects,
including hypoplasia similar to that observed in the taurine-deficient kitten. This paper reviews evidence that altered expression
of the renal taurine transporter may result in reduced intracellular taurine content, which in turn may lead to abnormal cell
volume regulation, cell death and, ultimately, defective renal development.
Received January 25, 2000/Accepted January 31, 2000 相似文献
5.
The intracellular level of taurine is maintained both by the taurine transporter (TAUT) and by endogenous synthesis from Met and Cys. We investigated in the present study the regulation of TAUT and of cysteine dioxygenase (CDO), one of the major taurine biosynthetic enzymes, in 3T3-L1 adipocytes. The TAUT activity, expression of TAUT and CDO mRNA were up-regulated by hypertonicity. In contrast, the TAUT activity, expression of TAUT and CDO mRNA were down-regulated by taurine-rich conditions. Furthermore, it was indicated that the up-regulation of TAUT activity resulted from the increased number of expressed TAUT, and not by the change in affinity of TAUT. On the other hand, the taurine-induced down-regulation of TAUT activity resulted not only from a decrease in the number of expressed TAUT but also from a decrease in their affinity. These results suggest that murine TAUT and CDO were cooperatively regulated in response to hypertonicity and taurine-rich conditions. 相似文献
6.
Polyene antibiotic amphotericin B in monomolecular layers: spectrophotometric and scanning force microscopic analysis 总被引:3,自引:0,他引:3
The effect of cytokines on the taurine uptake by human intestinal epithelial Caco-2 cells was investigated. Among the various cytokines tested, tumor necrosis factor alpha (TNF-alpha) markedly increased the taurine uptake by Caco-2 cells, resulting in an increase in the intracellular taurine level. TNF-alpha did not induce up-regulation of the taurine uptake in hepatic HepG2, renal human embryo kidney 293, and macrophage-like THP-1 cells. The uptake of glycine, L-leucine, and L-glutamic acid by Caco-2 cells was not affected by TNF-alpha. A kinetic analysis of the taurine uptake by TNF-alpha-treated Caco-2 cells suggests that this up-regulation was associated with both an increase in the amount of the taurine transporter (TAUT) and an increase in its affinity. TNF-alpha-treated cells showed a higher mRNA level of the TAUT than did the control cells. 相似文献
7.
Role of osmoregulation in the actions of taurine 总被引:7,自引:0,他引:7
Summary. Taurine regulates an unusual number of biological phenomena, including heart rhythm, contractile function, blood pressure,
platelet aggregation, neuronal excitability, body temperature, learning, motor behavior, food consumption, eye sight, sperm
motility, cell proliferation and viability, energy metabolism and bile acid synthesis. Many of these actions are associated
with alterations in either ion transport or protein phosphorylation. Although the effects on ion transport have been attributed
to changes in membrane structure, they could be equally affected by a change in the activity of the affected transporters.
Three common ways of altering transporter activity is enhanced expression, changes in the phosphorylation status of the protein
and cytoskeletal changes. Interestingly, all three events are altered by osmotic stress. Since taurine is a key organic osmolyte
in most cells, the possibility that the effects of taurine on ion transport could be related to its osmoregulatory activity
was considered. This was accomplished by comparing the effects of taurine, cell swelling and cell shrinkage on the activities
of key ion channels and ion transporters. The review also compares the phosphorylation cascades initiated by osmotic stress
with some of the phosphorylation events triggered by taurine depletion or treatment. The data reveal that certain actions
of taurine are probably caused by the activation of osmotic-linked signaling pathways. Nonetheless, some of the actions of
taurine are unique and appear to be correlated with its membrane modulating and phosphorylation regulating activities.
Received January 25, 2000/Accepted January 31, 2000 相似文献
8.
Taurine transporter is expressed in vascular smooth muscle cells 总被引:2,自引:0,他引:2
Summary. The regulation of vascular smooth muscle cells (VSMCs) function by taurine has been a subject of increasing interest and investigation,
and taurine is taken up into cells through a specific transporter system, the taurine transporter (TAUT). In the present study,
we examined the expression of TAUT in VSMCs and the kinetic parameters of the uptake process of TAUT in VSMCs. RT-PCR and
western blot demonstrated that the mRNA and protein of TAUT was expressed in VSMCs in vitro. Immunohistochemistry using antibody
for TAUT revealed the expression of this protein in rat thoracic aorta. The maximal [3H]taurine uptake rate in VSMCs was 37.75 ± 3.13 pmol/min per mg of protein, with a K
m
value of 5.42 ± 0.81 μM. Thus, VSMCs are able to express a functional taurine transporter. The regulation and detailed function
of taurine and TAUT in VSMCs remain unclear, but our findings suggest a functional role for them in VSMCs metabolism. 相似文献
9.
Yusuke GondoHideo Satsu Yoko IshimotoTaku Iwamoto Makoto Shimizu 《Biochemical and biophysical research communications》2012,426(3):433-437
Taurine (2-aminoethanesulfonic acid), a sulfur-containing β-amino acid, plays an important role in several essential biological processes; although, the underlying mechanisms for these regulatory functions remain to be elucidated, especially at the genetic level. We investigated the effects of taurine on the gene expression profile in Caco-2 cells using DNA microarray. Taurine increased the mRNA expression of thioredoxin interacting protein (TXNIP), which is involved in various metabolisms and diseases. β-Alanine or γ-aminobutyric acid (GABA), which are structurally or functionally related to taurine, did not increase TXNIP mRNA expression. These suggest the expression of TXNIP mRNA is induced specifically by taurine. β-Alanine is also known to be a substrate of taurine transporter (TAUT) and competitively inhibits taurine uptake. Inhibition of taurine uptake by β-alanine eliminated the up-regulation of TXNIP, which suggests TAUT is involved in inducing TXNIP mRNA expression. The up-regulation of TXNIP mRNA expression by taurine was also observed at the protein level. Furthermore, taurine significantly increased TXNIP promoter activity. Our present study demonstrated the taurine-specific phenomenon of TXNIP up-regulation, which sheds light on the physiological function of taurine. 相似文献
10.
Summary. Calcium ion (Ca2+) uptake was measured in rod outer segments (ROS) isolated from rat retina in the presence of varying concentrations of CaCl2 in the incubation buffer (1.0–2.5 mM). It is known that taurine increases Ca2+ uptake in rat ROS in the presence of ATP and at low concentrations of CaCl2 (Lombardini, 1985a); taurine produces no significant effects when CaCl2 concentrations are increased to 1.0 and 2.5 mM. With the removal of both taurine and ATP, Ca2+ uptake in rat ROS increased significantly in the presence of 2.5 mM CaCl2. Taurine treatment in the absence of ATP was effective in decreasing Ca2+ uptake at the higher levels of CaCl2 (2.0 and 2.5 mM). Similar effects were observed with ATP treatment. The data suggest that taurine and ATP, alone or in combination,
limit the capacity of the rat ROS to take up Ca2+ to the extent that a stable uptake level is achieved under conditions of increasing extracellular Ca2+, indicating a protective role for both agents against calcium toxicity.
Received January 25, 2000/Accepted January 31, 2000 相似文献
11.
高糖对培养大鼠心肌细胞牛磺酸转运的影响及其可能机制 总被引:1,自引:0,他引:1
目的:观察不同浓度葡萄糖对细胞牛磺酸(taurine)转运功能的影响。方法:在培养的大鼠心肌细胞上,用^3H标记的牛磺酸测定细胞牛磺酸转运和竞争性定量RTPCR测定细胞牛磺酸转运体(TAUT)mRNA含量。结果:不同浓度葡萄糖(10~30mmol/L)孵育,抑制细胞^3H-牛磺酸转运,呈时间依赖性。与对照组比较,高糖(20mmol/L和30mmol/L)使心肌细胞牛磺酸摄入量显著减少,其^3H-牛磺酸转运的最大速率(Vmax)减少,心肌细胞TAUTmRNA含量较对照组减少。结论:高糖抑制心肌细胞牛磺酸转运,这与TAUT的牛磺酸结合位点减少和TAUT基因转录水平下调有关。 相似文献
12.
自发性高血压大鼠心肌和血管组织牛磺酸的转运障碍 总被引:2,自引:0,他引:2
在自发性高血压大鼠(SHR)的心肌和主动脉血管组织上观察牛磺酸(taurine)转运和牛磺酸转运体(taurine transporter,TAUT) mRNA 的改变,结果显示,与对照组WKY大鼠相比,SHR组血浆牛磺酸水平和牛磺酸释放量增加,而心肌和血管组织牛磺酸水平和TAUT mRNA含量均降低,牛磺酸最大转运速率(Vmax)分别低24%和35%(P<0.05),米氏常数(Km)值分别高16%和39%(P<0.05),这些结果提示,SHR的心肌和血管组织牛磺酸转运障碍可能与TAUT活性和亲和力降低及TAUT基因水平的下调有关。 相似文献
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Summary. Taurine and glutamate were monitored by microdialysis technique during various cerebral insults: a. Application of K+ triggered a cortical spreading depression (CSD). Taurine and glutamate increased concomitantly but recovery of glutamate
was faster than that of taurine. b. Application of NMDA induced also CSD but only taurine increased. c. Induction of an infarct
triggered repetitive CSDs. Taurine increased rapidly whereas glutamate rose slowly starting with some delay. d. After induction
of ischemia, taurine and glutamate increased after onset of depolarisation. The increase of glutamate occurred late after
a small, transient increase in parallel with the depolarisation. These data suggest a close functional relationship between
the changes of both amino acids. Therefore, they should be monitored together especially in clinical settings: during excitation,
only taurine will increase; during overexcitation, taurine will also increase but to a higher maximum followed by a moderate
rise of glutamate; after energy failure, taurine will accumulate to its highest level followed by a continuous rise of glutamate.
Received January 25, 2000/Accepted January 31, 2000 相似文献
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Relationship of taurine and other amino acids in plasma and in neutrophils of septic trauma patients
Engel JM Mühling J Weiss S Kärcher B Löhr T Menges T Little S Hempelmann G 《Amino acids》2006,30(1):87-94
Summary. Recently, an interdependency of plasma taurine and other amino acids as well as metabolic and clinical variables implicating
therapeutic options was reported. This result may be an indication that plasma taurine levels are directly related to intracellular
levels. Therefore, the aim of this study was to analyse the possible relationship between taurine levels in plasma and in
neutrophils, the relationship to other amino acids, and variables quantifying metabolic impairment and severity of sepsis
in multiple trauma patients developing sepsis. After multiple trauma taurine decreased significantly in plasma in thirty-two
patients as well as within the neutrophil and does not recover in sepsis. Lower individual levels in the neutrophil did not
follow lower individual levels in plasma and no correlation of taurine in plasma and in the neutrophils could be observed.
In sepsis, only plasma showed an interdependency of taurine, aspartate, and glutamate. No association between taurine plasma
or intracellular levels and SOFA score as indicator for severity of sepsis or metabolic variables was observed. After multiple
trauma and in sepsis, taurine uptake in cells (which is regulated in different ways), and intracellular taurine (which serves
e.g. as an osmolyte) can be influenced. Therefore a prediction of the neutrophil taurine pool seems not fully possible from
taurine plasma levels. Intracellular taurine has some unique properties explaining the missing interdependency despite some
similarities in osmoregulation and metabolic interactions to other amino acids. The association of taurine, aspartate, and
glutamate in plasma cannot be simply transferred to the neutrophils intracellular level. The clinical meaning of the plasma
correlation remains unclear. A dependency of plasma and neutrophil taurine to severity of sepsis and to metabolic variables
seems not possible because of the multifactorial pathophysiology of sepsis. 相似文献
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Summary. Previously we have observed the lack of immunoreactivity of taurine in the rod outer segments from light-adapted fish, such
as the ayu Plecoglossus altivelis and lefteye flounder Paralichthys olivaceus. This finding prompted us to investigate if there is a difference in the immunocytochemical localization of taurine in the
rod outer segments between the dark- and light-adapted states. In the retinas of the glass eel Anguilla japonica and the young goldfish Carassius auratus, extremely intense immunostaining was found in the cone outer segments, rod inner segments, photoreceptor supranuclear region
and outer plexiform layer. The rod outer segments were not immunostained in the light-adapted state, while they were intensely
immunostained in the dark-adapted state. Consequently, it was suggested that the lack of immunoreactivity in the rod outer
segment may depend on light stimulation. In addition, the conspicuous immunocytochemical localization of taurine was discussed
with the possible functional roles for taurine in the fish retina.
Received January 25, 2000/Accepted January 31, 2000 相似文献
17.
Summary. Taurine has been reported to enhance cholesterol 7α-hydroxylase (CYP7A1) mRNA expression in animal models. However, no in vitro studies of this effect have been reported. The Hep G2 human hepatoma cell line has been recognized as a good model for studying
the regulation of human CYP7A1. This work characterizes the effects of taurine on CYP7A1 mRNA levels of Hep G2 cells in a
dose- and time-dependent manner. In the dose-dependent experiment, Hep G2 cells were treated with 0, 2, 10 or 20 mM taurine
in the presence or absence of cholesterol 0.2 mM for 48 h. In the time-dependent experiment, Hep G2 cells were treated with
0 or 20 mM taurine for 4, 24 and 48 h with and without cholesterol 0.2 mM. Our data revealed that taurine showed time- and
dose-response effects on CYP7A1 mRNA levels in Hep G2 cells. However, glycine – a structural analogue of taurine – did not
have an effect on CYP7A1 gene expression. These results show that, in agreement to previous studies on animal models, taurine
induces the mRNA levels of CYP7A1 in Hep G2 cells, which could enhance cholesterol conversion into bile acids. Also, Hep G2
cell line may be an appropriate model to study the effects of taurine on human cholesterol metabolism. 相似文献
18.
Summary. We have recently reported that the nitric oxide (NO) donor, sodium nitroprusside (SNP), induces seizures which are associated
with an increase in the basal release of aspartate and glutamate from rat hippocampus (Kaku et al., 1998). In order to determine
whether taurine release occurs with SNP-induced seizures, we examined the effects of NO-related compounds, i.e., the NO trapper,
diethyldithiocarbamate (DETC), the superoxide radical scavenger, dithiothreitol (DTT), the xanthine oxidase inhibitor, oxypurinol
and the guanylyl cyclase inhibitor, 1H-(1,2,4)oxadiazole(4,3-a)quinoxalin-1-one (ODQ), on SNP-induced seizures and in vivo taurine release from rat hippocampus using microdialysis. Perfusion with 0.5 mM SNP provoked seizures and significantly increased
taurine release, with the increase in release occurring primarily during reperfusion with artificial cerebrospinal fluid lacking
SNP. Perfusion with 5 mM DETC significantly abolished the SNP-induced seizures and reduced taurine release during and after
perfusion with the drugs. Perfusion with 1 mM DTT significantly reduced both the frequency of the SNP-induced seizures and
taurine release during and after perfusion with the drugs. Perfusion with 1 mM oxypurinol or 0.5 mM ODQ did not reduce the
frequency of the SNP-induced seizures, but tended to decrease taurine release during and after perfusion with the drugs. These
results demonstrate that SNP-induced seizures are triggered by an increase in both NO and peroxynitrite and are related to
an increase in taurine release from rat hippocampus.
Received January 25, 2000/Accepted January 31, 2000 相似文献
19.
Summary. The effect of dietary sulfur amino acids on the taurine content of rat blood and tissues was investigated. Three types of
diet were prepared for this study: a low-taurine diet (LTD), normal taurine diet (NTD; LTD + 0.5% Met), and high-taurine diet
(HTD; LTD + 0.5% Met + 3% taurine). These diets had no differing effect on the growth of the rats. The concentration of taurine
in the blood from the HTD- and NTD-fed rats was respectively 1,200% and 200% more than that from LTD-. In such rat tissues
as the liver, the taurine content was significantly affected by dietary sulfur amino acids, resulting in a higher content
with HTD and lower content with LTD. However, little or no effect on taurine content was apparent in the heart or eye. The
activity for taurine uptake by the small intestine was not affected by dietary sulfur amino acids. The expression level of
taurine transporter mRNA was altered only in the kidney under these dietary conditions: a higher expression level with LTD
and lower expression level with HTD.
Received January 8, 2002 Accepted January 18, 2002 Published online August 20, 2002
Authors' address: Dr. Hideo Satsu, Laboratory of Food Chemistry, Department of Applied Biological Chemistry, Graduate School of Agricultural
and Life Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan, Fax: +81-3-5841-8026 E-mail: asatsu@mail.ecc.u-tokyo.ac.jp
Abbreviations: HTD, high-taurine diet; NTD, normal taurine diet; LTD, low-taurine diet; TAUT, taurine transporter; CSA, cysteine sulfinate;
CDO, cysteine dioxygenase; CSAD, cysteine sulfinate decarboxylase; PBS, phosphate-buffered saline; DIDS, 4,4′-diisothiocyanostilbene-2′,2′-disulfonic
acid 相似文献
20.
Interaction between the actions of taurine and angiotensin II 总被引:1,自引:0,他引:1
Summary. The amino acid, taurine, is an important nutrient found in very high concentration in excitable tissue. Cellular depletion
of taurine has been linked to developmental defects, retinal damage, immundeficiency, impaired cellular growth and the development
of a cardiomyopathy. These findings have encouraged the use of taurine in infant formula, nutritional supplements and energy
promoting drinks. Nonetheless, the use of taurine as a drug to treat specific diseases has been limited. One disease that
responds favorably to taurine therapy is congestive heart failure. In this review, we discuss three mechanisms that might
underlie the beneficial effect of taurine in heart failure. First, taurine promotes natriuresis and diuresis, presumably through
its osmoregulatory activity in the kidney, its modulation of atrial natriuretic factor secretion and its putative regulation
of vasopressin release. However, it remains to be determined whether taurine treatment promotes salt and water excretion in
humans with heart failure. Second, taurine mediates a modest positive inotropic effect by regulating [Na+]i and Na+/Ca2+ exchanger flux. Although this effect of taurine has not been examined in human tissue, it is significant that it bypasses
the major calcium transport defects found in the failing human heart. Third, taurine attenuates the actions of angiotensin
II on Ca2+ transport, protein synthesis and angiotensin II signaling. Through this mechanism taurine would be expected to minimize many
of the adverse actions of angiotensin II, including the induction of cardiac hypertrophy, volume overload and myocardial remodeling.
Since the ACE inhibitors are the mainstay in the treatment of congestive heart failure, this action of taurine is probably
very important.
Received November 10, 1998, Accepted May 19, 1999 相似文献