Search PubMed⌕ Search

Biomedical subjects

Y Tang

Publications and source records attributed to Y Tang.

At least 325 records · Page 18Linked to original sources

Further evidence linking urolithiasis and blood coagulation: urinary prothrombin fragment 1 is present in stone matrix.

The fact that organic material is always present and distributed throughout each renal calculus suggests that it may play a role in stone formation. The organic matrix of calcium oxalate (CaOx) crystals freshly generated in urine in vitro contains urinary prothrombin fragment 1 (UPTF1) as the principal protein. In this initial study, matrix was extracted from 12 renal calculi and evaluated for the presence of UPTF1 using Western blotting. UPTF1 was present in all eight stones whose principal component was CaOx, and in one of two stones which consisted mainly of calcium phosphate (CaP). UPTF1 was absent from the two struvite calculi examined. The relationship between CaP and UPTF1 was explored further. Matrix harvested from CaP crystals freshly generated in urine in vitro was also shown to contain UPTF1 as its principal component. Our inability to detect UPTF1 in one mixed CaOx/CaP stone may be related to our methods of matrix retrieval, while its absence from two struvite stones argues against it being present in the other stones merely as a consequence of passive inclusion. This absence may be related to the alkaline environment typical of struvite stone growth. The finding that UPTF1 is present in some renal stones provides the first direct evidence that links blood coagulation proteins with urolithiasis.

Adult↗

The genital atrium as a new character for distinguishing parous and nulliparous Neotropical sandflies.

Changes in the appearance of the membrane delimiting the genital atrium of Lutzomyia migonei are described for the first time. Dissections of laboratory-bred females at different physiological stages (i.e. on emergence, after a bloodmeal and after oviposition) revealed clear and constant differences between the membranes of the parous and nulliparous flies. The state of the membrane can be used as an alternative method for accurately age-grading female sandflies. Dissection methods and a simplified technique to prepare parts of sandflies for examination in a scanning electron microscope are also presented.

Animals↗

Calcium dynamics and homeostasis in a mathematical model of the principal cell of the cortical collecting tubule.

Calcium (Ca) dynamics are incorporated into a mathematical model of the principal cell in the cortical collecting tubule developed earlier in Strieter et al. (1992a. Am. J Physiol. 263:F1063-1075). The Ca components are modeled after the Othmer-Tang model for IP(3)-sensitive calcium channels (1993, in Experimental and Theoretical Advances in Biological Pattern Formation, 295-319). There are IP(3)-sensitive Ca channels and ATP-driven pumps on the membrane of the endoplasmic reticulum. Calcium enters the cell passively down its electrochemical gradient. A Ca pump and Na/Ca exchange in the basolateral membrane are responsible for the extrusion of cytoplasmic calcium. Na/Ca exchange can also operate in reverse mode to transport Ca into the cell. Regulatory effects of cytoplasmic Ca on the apical Na channels are modeled after experimental data that indicate apical Na permeability varies inversely with cytoplasmic Ca concentration. Numerical results on changes in intracellular Ca caused by decreasing NaCl in the bath and the lumen are similar to those from experiments in Bourdeau and Lau (1990. Am. J Physiol. 258:F1497-1503). This match of simulation and experiment requires the synergistic action of the Na/Ca exchanger and the Ca regulated apical Na permeability. In a homogeneous medium, cytoplasmic Ca becomes oscillatory when extracellular Na is severely decreased, as observed in experiments of cultured principal cells (Koster, H., C. van Os and R. Bindels. 1993. Kidney Int.43:828-836). This essentially pathological situation arises because the hyperpolarization of membrane potential caused by Na-free medium increases Ca influx into the cell, while the Na/Ca exchanger is inactivated by the low extracellular Na and can no longer move Ca out of the cell effectively. The raising of the total amount of intracellular Ca induces oscillatory Ca movement between the cytoplasm and the endoplasmic reticulum. Ca homeostasis is investigated under the condition of severe extracellular Ca variations. As extracellular Ca is decreased, Ca regulation is greatly impaired if Ca does not regulate apical ionic transport. The simulations indicate that the Na/Ca exchanger alone has only limited regulatory capacity. The Ca regulated apical sodium or potassium permeability are essential for regulation of cytoplasmic Ca in the principal cell of the cortical collecting tubule.

Calcium↗

Establishment of monoclonal antibodies against human erythrocyte NADH-cytochrome b5 reductase.

NADH-cytochrome b5 reductase (b5R) is a multifunctional redox enzyme, whose deficiency leads to hereditary methemoglobinemia. By using recombinant human red cell b5R as antigen to immunize BALB/c mice and conventional cell fusion, we have established two mouse hybridoma cell lines secreting IgG monoclonal antibodies (MAbs) to b5R. In immunoblotting, the MAbs were shown to react specifically with b5R. They were also found to be capable of capturing b5R activity from b5R solution and normal human hemolysate. It was implied that the binding sites of the MAbs might not be proximal to the active site of the enzyme, but might be in close proximity to each other. The MAbs will be useful in b5R-related investigations.

Antibodies, Monoclonal↗

Position-dependent protein mutant profile based on mean force field calculation.

The application of the mean force field in protein mutant stability prediction is explored. Based on protein main chain characteristics, including polar fraction, accessibility and dihedral angles, the mean force field was constructed to evaluate the compatibility between an amino acid residue and its environment, from which a position-dependent protein mutant profile was constructed. At each position along a protein sequence, the native residue was replaced by the other 19 types of amino acid residues. The matches were evaluated by energies from mean force field calculation, from which a mutant profile along the protein sequence was derived. General characteristics of such a profile were analyzed. Mutant stabilities for two sets of mutants in two proteins were found to be reasonable compared with experimental data, which indicates that the present method can act as a guide in protein engineering and as an effective scoring matrix in protein sequence-structure alignment studies.

Amino Acid Sequence↗

Localization of quinolinic acid in the murine AIDS model of retrovirus-induced immunodeficiency: implications for neurotoxicity and dendritic cell immunopathogenesis.

OBJECTIVE AND DESIGN: Using murine AIDS (MAIDS) as a model of retrovirus-induced immunodeficiency, the aims of this study were (1) to determine the cellular source(s) of quinolinic acid (Quin) with regard to its significance as a potential neuroexcitotoxin in AIDS dementia complex, and (2) to characterize the relationship between dendritic cell Quin immunoreactivity and the histopathological changes associated with the progression of disease. METHODS: Mice with MAIDS were sacrificed from 1 to 16 weeks post-infection. Temporal and spatial changes in the in vivo distribution of Quin at the cellular level were determined by carbodiimide-based immunohistochemical methods. RESULTS: Cellular Quin immunoreactivity was chronically elevated in lymphoid tissues of mice with MAIDS. In contrast, no cellular Quin immunoreactivity was visible in the brain parenchyma at any timepoint studied. CONCLUSION: These findings are consistent with the view that select immune cells in the peripheral lymphoid tissues may be the primary source of Quin, which may contribute to neurotoxic complications in retrovirus-induced immunodeficiency syndromes. The predominant Quin immunoreactive cell types changed with the progression of disease. A significant finding was the marked increase in the number of Quin immunoreactive dendritic cells in the early phase of MAIDS, suggesting a relationship between dendritic cells and Quin in retroviral infection.

AIDS Dementia Complex↗

Rapid nitric oxide- and prostaglandin-dependent release of calcitonin gene-related peptide (CGRP) triggered by endotoxin in rat mesenteric arterial bed.

1. Our objective was to determine whether endotoxin (ETX) could directly trigger the release of calcitonin gene-related peptide (CGRP) from perivascular sensory nerves in the isolated mesenteric arterial bed (MAB) of the rat and to determine whether nitric oxide (NO) and prostaglandins (PGs) are involved. 2. ETX caused time- and concentration-dependent release of CGRP, and as much as a 17 fold increase in CGRP levels in the perfusate at 10-15 min after the administration of ETX (50 micrograms ml-1). 3. CGRP-like immunoreactivity in the perfusate was shown to co-elute with synthetic rat CGRP by reverse-phase h.p.l.c. 4. Pretreatment of MAB with capsaicin or ruthenium red inhibited ETX-induced CGRP release by 90% and 71%, respectively. ETX-evoked CGRP release was decreased by 84% during Ca2(+)-free perfusion. 5. The release of CGRP evoked by ETX was enhanced by L-arginine by 43% and inhibited by N omega-nitro-L-arginine (L-NOARG) and methylene blue by 37% and 38%, respectively. L-Arginine reversed the effect of L-NOARG. 6. Indomethacin and ibuprofen also inhibited the ETX-induced CGRP release by 34% and 44%, respectively. No additive inhibition could be found when L-NOARG and indomethacin were concomitantly incubated. 7. The data suggest that ETX triggers the release of CGRP from capsaicin-sensitive sensory nerves innervating blood vessels. The ETX-induced CGRP release is dependent on extracellular Ca2+ influx and involves a ruthenium red-sensitive mechanism. Both NO and PGs appear to be involved in the ETX-induced release of CGRP in the rat mesenteric arterial bed.

Animals↗

Upstream interactions at the lambda pRM promoter are sequence nonspecific and activate the promoter to a lesser extent than an introduced UP element of an rRNA promoter.

The rightward regulatory region of bacteriophage lambda contains two promoters, pRM and pR, which direct the synthesis of nonoverlapping divergent transcripts from start sites 82 bp apart. Each of the two promoters has an upstream (A+T)-rich region (ATR) within the sequence from -40 to -60 where in the rrnB P1 promoter a stretch of 20 (A+T) bp greatly stimulates promoter function. Here we present an investigation of the possible functional significance of pRM's ATR. We determined the effects on RNA polymerase-pRM promoter interaction both of (G+C) substitutions in the ATR and of amino acid substitutions in the alpha subunit, known to affect the upstream interaction. We find small (two- to threefold) effects of selected mutations in the alpha subunit on open complex formation at pRM. However, the (presumably upstream) interactions underlying these effects are sequence nonspecific, as they are not affected by (G+C) substitutions in the ATR. Substitution of the 20-bp UP element of the rrnB P1 promoter between positions -40 and -60 at pRM stimulates open complex formation to a considerably greater extent (5- to 10-fold). Results from kinetic studies indicate that on this construct the UP element mainly accelerates a step subsequent to the binding of RNA polymerase, although it may also facilitate the binding event itself. Less extensive studies likewise provide evidence for a two- to threefold activation of pR by upstream interactions. The possible involvement of the alpha subunit in the previously characterized (e.g., B. C. Mita, Y. Tang, and P. L. deHaseth, J. Biol. Chem. 270:30428-30433, 1995) interference of pR-bound RNA polymerase with open complex formation at pRM is discussed.

Amino Acid Sequence↗

Dot-immunogold filtration assay as a screening test for syphilis.

A dot-immunogold filtration assay (DIGFA) for the rapid detection of reaginic antibody in the serum of syphilitic patients was developed. The assay was simple, rapid, and reproducible. The test completion time was 2 min, and the assay required no equipment. The positive dot was very obvious, and the results could easily be determined with the naked eye. A total of 350 serum samples were examined by DIGFA, the rapid plasma reagin test, and the fluorescent treponemal antibody-absorption test. The levels of agreement between DIGFA and the rapid reagin test and between DIGFA and the fluorescent treponemal antibody-absorption test were 100 and 98%, respectively. The results of clinical application indicated that DIGFA could be used as a routine screening test for syphilis.

Antibodies, Bacterial↗

ATP-dependent release of glucocorticoid receptors from the nuclear matrix.

Glucocorticoid receptors (GRs) have the capacity to shuttle between the nuclear and cytoplasmic compartments, sharing that trait with other steroid receptors and unrelated nuclear proteins of diverse function. Although nuclear import of steroid receptors, like that of nearly all other karyophilic proteins examined to date, requires ATP, there appear to be different energetic requirements for export of proteins, including steroid receptors, from nuclei. In an attempt to reveal which steps, if any, in the nuclear export pathway utilized by steroid receptors require ATP, we have used indirect immunofluorescence to visualize GRs within cells subjected to a reversible ATP depletion. Under conditions which lead to >95% depletion of cellular ATP levels within 90 min, GRs remain localized within nuclei and do not efflux into the cytoplasm. Under analogous conditions of ATP depletion, transfected progesterone receptors are also retained within nuclei. Importantly, GRs which accumulate within nuclei of ATP-depleted cells are distinguished from nuclear receptors in metabolically active cells by their resistance to in situ extraction with a hypotonic, detergent-containing buffer. GRs in ATP-depleted cells are not permanently trapped in this nuclear compartment, as nuclear receptors rapidly regain their capacity to be extracted upon restoration of cellular ATP, even in the absence of de novo protein synthesis. More extensive extraction of cells with high salt and detergent, coupled with DNase I digestion, established that a significant fraction of GRs in ATP-depleted cells are associated with an RNA-containing nuclear matrix. Quantitative Western blot (immunoblot) analysis confirmed the dramatic increase in GR binding to the nuclear matrix of ATP-depleted cells, while confocal microscopy revealed that GRs are bound to the matrix throughout all planes of the nucleus. ATP depletion does not lead to wholesale collapse of nuclear proteins onto the matrix, as the interaction of a subpopulation of simian virus 40 large tumor antigen with the nuclear matrix is not quantitatively altered in ATP-depleted Cos-1 cells. Nuclear GRs which are not bound to the nuclear matrix of metabolically active cells (i.e., a DNA-binding domain deletion mutant and a beta-galactosidase chimera possessing the GR nuclear localization signal sequence) are not recruited to the matrix upon depletion of cellular ATP. Thus, it appears that ATP depletion does not expose the GR to nuclear matrix interactions which are not normally encountered in cells but merely alters the dynamics of such interactions. The dynamic association of steroid receptors with the nuclear matrix may provide a mechanism which is utilized by these regulable transcription factors to facilitate their efficient scanning of the genome.

Adenosine Triphosphate↗

The effects of salinity change on the exercise performance of two Atlantic cod (Gadus morhua) populations inhabiting different environments

The objective of this study was to determine whether differences in exercise physiology between Atlantic cod (Gadus morhua) populations from different salinity environments could be changed by acclimating individuals of each population to the natural salinity of the comparison population. The exercise-associated blood chemistry of cod from the brackish Bras d'Or lakes, which had previously been shown to be quite different from that of 'open-ocean' cod, changed to resemble the blood chemistry of their oceanic relatives after only 2 months of acclimation to full-strength salinity. In contrast, the blood chemistry of cod from the Scotian Shelf of the Northwest Atlantic Ocean showed little change after 2 months of acclimation to brackish water. These results demonstrate that the degree of osmoconformity to changes in environmental salinity is a population-specific not a species-specific trait. The blood chemistry differences between populations and salinities did not translate into differences in exercise performance: i.e. critical swimming speeds were statistically uniform across all combinations of population and salinity, although performance was more varied in fish swimming in 'non-native' waters. Other 'whole-animal' physiological characteristics, such as metabolic rate and the aerobic cost of transport, were dependent upon both population origin and the environmental salinity. Vigorous swimming was more energetically expensive at full-strength salinity than at 20 salinity, yet estimates of standard (i.e. resting) metabolic rate were lower for full-strength salinity. Environmental salinity also influenced the relative appearance of lactate and metabolic acid in the extracellular fluid compartment, with full-strength salinity favouring the relative appearance of lactate in the blood. Multivariate statistical analyses of this data set showed that, in contrast to other fish species and studies, differences in blood oxygen transport appear to account for some of the swimming performance differences seen in Atlantic cod at 2 °C. The two experimental populations were cleanly separated by a principal components analysis, regardless of the salinity to which they were acclimated, confirming our earlier contention that these cod populations are physiologically distinct. A key feature of that distinctness is the greater phenotypic plasticity exhibited by the population from the more euryhaline, more eurythermal environment.

Journal Article↗

The value of MR urography that uses HASTE sequences to reveal urinary tract disorders.

OBJECTIVE: Breath-hold MR urography using half-Fourier acquisition single-shot turbo spin-echo (HASTE) sequences was evaluated as a noninvasive alternative to excretory urography in healthy volunteers and in patients with disorders of the urinary tract. SUBJECTS AND METHODS: Twenty healthy volunteers and 45 patients with disorders of the urinary tract underwent HASTE MR urography on a 1.5-T MR imaging unit. Imaging time was 2 sec for single-thick-slice (20- to 60-mm slice thickness) technique and 10-18 sec for multislice technique. In the latter, images were postprocessed with maximum-intensity-projection technique and visualized in an arbitrary plane. Obstruction and its level were determined solely by excretory urography in eight patients, by excretory urography with other imaging techniques (CT, retrograde pyelography, or sonography) in 27 patients, and by sonography alone in the 20 normal volunteers, seven pregnant women, and three patients who were allergic to iodinated contrast media. We evaluated whether HASTE MR urograms showed obstruction, showed the level of obstruction, and showed the cause of obstruction. RESULTS: In all 20 healthy volunteers and all 45 patients, the upper, middle, and lower group of renal calices and the pelvis were clearly revealed by HASTE MR urography. In patients whose urinary tracts were seen on excretory urography (n = 31), the accuracy of HASTE MR urography in revealing urinary tract dilatation and level of obstruction completely correlated with that of excretory urography, although functional information about the obstructed collecting system was not obtained. However, MR urography revealed nonfunctioning urinary tracts that were invisible on excretory urography (n = 6). In patients with extrinsic obstruction (n = 27), MR urography also revealed the obstructing lesions. Small stones within the ureter were more clearly seen on single-shot or source images. With HASTE MR urography, hydronephrosis in pregnant women (n = 7) was clearly shown. CONCLUSION: HASTE MR urography can be used as an alternative to excretory urography to obtain high-quality images of the dilated urinary tract and adjacent abnormalities. HASTE MR urography allows rapid acquisition of images, thus overcoming the drawbacks of earlier MR urography techniques.

Adolescent↗

Frequencies and genetic diversity of major histocompatibility complex class II haplotypes in commercial turkey lines.

The purpose of the present study was to estimate frequencies and diversity of MHC haplotypes in primary breeding lines of commercial turkeys. Restriction fragment length polymorphism analysis was used to assay MHC Class II haplotypes of blood samples from 11 primary breeding lines (comprised of both sire and dam lines) contributed by three major turkey breeding companies. Twenty-five blood samples obtained from wild turkeys were included for comparison. Seven haplotypes previously identified in experimental turkey lines were detected in the commercial lines. One haplotype, A, was predominant in all commercial lines with an average frequency of 76% and in the wild turkeys with a frequency of 46%. Diversity of MHC haplotypes was reduced in the commercial lines compared with the wild turkey. Seven commercial lines had no more than four haplotypes and loci in some lines were close to fixation. Haplotypic frequencies among sire and dam lines differed significantly, but genetic diversity was not different. Only Haplotype D was significantly more frequent in sire than in dam lines. The present data demonstrate that genetic diversity at MHC loci was low in commercial turkey lines.

Animal Husbandry↗

Molecular modeling of interactions between tetrahydroprotoberberines and dopamine receptors.

AIM: To build up the structure models of dopamine receptors, then combined with the receptor models, to investigate the action mechanism of tetrahydroprotoberberines (THPB) on dopamine receptors at the molecular level. METHODS: Using the three-dimensional structure of bacteriorhodopsin as a template, we have constructed dopamine D1 and D2 receptor models on computer. l-Stepholidine was selected as the leading compound of THPB and docked into D1 and D2 receptor active sites. RESULTS: After manual adjustment and energy minimization, the ligand-receptor interaction models were achieved. Based on these models, the possible action mechanism of THPB on dopamine receptors was suggested that the protonated N atom of THPB form electrostatic interaction and hydrogen-bonding interaction with residue Asp in TM3 of the receptor, the two substituents in D ring of THPB form hydrogen-bonding interactions with two Ser residues in TM5 of the receptor, and the aryl groups form pi-pi interactions with some aryl residues of the receptor around ligand. CONCLUSION: Our ligand-receptor interaction models should be helpful for rational design of more potent drugs.

Amino Acid Sequence↗

Secretory expression of a single-chain insulin precursor in yeast and its conversion into human insulin.

A synthetic single-chain porcine insulin precursor (PIP) gene and an alpha-mating factor leader sequence (alpha MFL) gene obtained by the PCR method are inserted between the promoter and 3'-terminating sequence of the alcohol dehydrogenase gene ADH1 in plasmid pVT102-U to form plasmid pVT102-U/alpha MFL-PIP. The single-chain insulin precursor is expressed and secreted to the culture medium by Saccharomyces cerevisiae transformed by pVT102-U/alpha MFL-PIP. The precursor is purified and converted into human insulin by tryptic transpeptidation. The purified human insulin is fully active and can be crystallized. The overall yield of human insulin is 25 mg per liter of culture medium.

Base Sequence↗

[Clinical observation on effect of yiqi huoxue decoction over the left ventricular diastolic dysfunction].

The left ventricular diastolic function, grade of heart function and degree of Heart-Qi Deficiency of 52 aged patients with left ventricular diastolic dysfunction (LVDD) were measured by means of Doppler echocardiography and left ventricular impedance cardiography before and after treatment with Buqi Qiangxin decoction (BQQXD), a recipe of TCM for reinforcing Qi and promoting blood circulation. The data were compared with that of control group (15 cases) treated with verapamil. Results showed that 92.3% of the LVDD patients were associated with Heart-Qi Deficiency and 69.2% were complicated with blood stasis. After treated with BQQXD, the grade of heart function was elevated in 82.6%, the degree of Heart-Qi Deficiency was improved in 89.6% of the patients. The parameters reflecting the left ventricular diastolic function were all improved in different degree (P < 0.05-0.01), but the parameters reflecting left ventricular compliance were changed insignificantly (P > 0.05). It indicated that besides controlling on the etiological factors, the mechanism of BQQXD in treating left ventricular dysfunction might be related with its calcium antagonistic effect.

Aged↗