Determinants of Brushite Stone Formation: A Case-Control Study

Purpose

The occurrence of brushite stones has increased during recent years. However, the pathogenic factors driving the development of brushite stones remain unclear.

Methods

Twenty-eight brushite stone formers and 28 age-, sex- and BMI-matched healthy individuals were enrolled in this case-control study. Anthropometric, clinical, 24 h urinary parameters and dietary intake from 7-day weighed food records were assessed.

Results

Pure brushite stones were present in 46% of patients, while calcium oxalate was the major secondary stone component. Urinary pH and oxalate excretion were significantly higher, whereas urinary citrate was lower in patients as compared to healthy controls. Despite lower dietary intake, urinary calcium excretion was significantly higher in brushite stone patients. Binary logistic regression analysis revealed pH>6.50 (OR 7.296; p = 0.035), calcium>6.40 mmol/24 h (OR 25.213; p = 0.001) and citrate excretion <2.600 mmol/24 h (OR 15.352; p = 0.005) as urinary risk factors for brushite stone formation. A total of 56% of patients exhibited distal renal tubular acidosis (dRTA). Urinary pH, calcium and citrate excretion did not significantly differ between patients with or without dRTA.

Conclusions

Hypercalciuria, a diminished citrate excretion and an elevated pH turned out to be the major urinary determinants of brushite stone formation. Interestingly, urinary phosphate was not associated with urolithiasis. The increased urinary oxalate excretion, possibly due to decreased calcium intake, promotes the risk of mixed stone formation with calcium oxalate. Neither dietary factors nor dRTA can account as cause for hypercalciuria, higher urinary pH and diminished citrate excretion. Further research is needed to define the role of dRTA in brushite stone formation and to evaluate the hypothesis of an acquired acidification defect.     

Isolation of plasma albumin by ethanol extraction is inappropriate for isotope ratio measurements during the acute phase response

Isolation of high-purity albumin from plasma is essential to study albumin kinetics in vivo with tracer techniques. Because of its simplicity ethanol extraction has been repeatedly used for albumin purification. However, it cannot be excluded that this single-step procedure completely prohibits contamination by other proteins, especially those known to be produced at an accelerated rate during the acute phase response. In the present study, we wanted to examine the reliability of ethanol extraction in different clinical conditions and to study the effects of potential impurities on albumin enrichment during stable isotope tracer studies. SDS-PAGE revealed a contaminating protein band at about 25,000 Da in healthy subjects and postoperative patients during the acute phase response, but not in critically ill patients. According to densitometry about 8% of proteins after ethanol extraction were contaminants. To examine potential contaminant effects on tracer enrichment 1-[13C]-leucine was given to healthy subjects and postoperative patients. Blood samples were taken after various amounts of time, and albumin enrichments (tracer/tracee ratios) were determined from isotope ratios obtained by mass spectrometry. Irrespective of the magnitude of tracer enrichment, postoperative tracer/tracee ratios were significantly higher (on average +10%) in samples exclusively analysed by ethanol extraction than in samples which had undergone additional electrophoretic purification. No significant effect of the contaminant was seen in healthy subjects. N-terminal protein sequencing revealed contaminants to mainly consist of apolipoprotein A-1. Its physiology and pathophysiology may sufficiently explain its variable effects of albumin enrichment. Our findings suggest that exclusive ethanol extraction is inappropriate for albumin isolation in tracer studies performed during the acute phase response. Ethanol extraction may also not be advisable in all other situations known to be associated with a rise in apolipoprotein A-1 turnover.     

Re-interpreting the role of endo-��-mannanases as mannan endotransglycosylase/hydrolases in the plant cell wall

Background

Mannans are hemicellulosic polysaccharides in the plant primary cell wall with two major physiological roles: as storage polysaccharides that provide energy for the growing seedling; and as structural components of the hemicellulose–cellulose network with a similar function to xyloglucans. Endo-β-mannanases are hydrolytic enzymes that cleave the mannan backbone. They are active during seed germination and during processes of growth or senescence. The recent discovery that endo-β-mannanase LeMAN4a from ripe tomato fruit also has mannan transglycosylase activity requires the role of endo-β-mannanases to be reinterpreted.

Aims

In this review, the role of endo-β-mannanases as mannan endotransglycosylase/hydrolases (MTHs) in remodelling the plant cell wall is considered by analogy to the role of xyloglucan endotransglucosylase/hydrolases (XTHs). The current understanding of the reaction mechanism of these enzymes, their three-dimensional protein structure, their substrates and their genes are reported.

Future outlook

There are likely to be more endohydrolases within the plant cell wall that can carry out hydrolysis and transglycosylation reactions. The challenge will be to demonstrate that the transglycosylation activities shown in vitro also exist in vivo and to validate a role for transglycosylation reactions during the growth and development of the plant cell wall.Key words: Cell wall, endo-β-mannanase, endohydrolase, mannan, endotransglycosylase     

99mTc-Labeled HYNIC-DAPI Causes Plasmid DNA Damage with High Efficiency

^99mTc is the standard radionuclide used for nuclear medicine imaging. In addition to gamma irradiation, ^99mTc emits low-energy Auger and conversion electrons that deposit their energy within nanometers of the decay site. To study the potential for DNA damage, direct DNA binding is required. Plasmid DNA enables the investigation of the unprotected interactions between molecules and DNA that result in single-strand breaks (SSBs) or double-strand breaks (DSBs); the resulting DNA fragments can be separated by gel electrophoresis and quantified by fluorescent staining. This study aimed to compare the plasmid DNA damage potential of a ^99mTc-labeled HYNIC-DAPI compound with that of ^99mTc pertechnetate (^99mTcO₄⁻). pUC19 plasmid DNA was irradiated for 2 or 24 hours. Direct and radical-induced DNA damage were evaluated in the presence or absence of the radical scavenger DMSO. For both compounds, an increase in applied activity enhanced plasmid DNA damage, which was evidenced by an increase in the open circular and linear DNA fractions and a reduction in the supercoiled DNA fraction. The number of SSBs elicited by ^99mTc-HYNIC-DAPI (1.03) was twice that caused by ^99mTcO₄⁻ (0.51), and the number of DSBs increased fivefold in the ^99mTc-HYNIC-DAPI-treated sample compared with the ^99mTcO₄⁻ treated sample (0.02 to 0.10). In the presence of DMSO, the numbers of SSBs and DSBs decreased to 0.03 and 0.00, respectively, in the ^99mTcO₄^– treated samples, whereas the numbers of SSBs and DSBs were slightly reduced to 0.95 and 0.06, respectively, in the ^99mTc-HYNIC-DAPI-treated samples. These results indicated that ^99mTc-HYNIC-DAPI induced SSBs and DSBs via a direct interaction of the ^99mTc-labeled compound with DNA. In contrast to these results, ^99mTcO₄⁻ induced SSBs via radical formation, and DSBs were formed by two nearby SSBs. The biological effectiveness of ^99mTc-HYNIC-DAPI increased by approximately 4-fold in terms of inducing SSBs and by approximately 10-fold in terms of inducing DSBs.     

A Phase I Clinical Trial of Systemically Delivered NEMO Binding Domain Peptide in Dogs with Spontaneous Activated B-Cell like Diffuse Large B-Cell Lymphoma

Activated B-Cell (ABC) Diffuse Large B-Cell Lymphoma (DLBCL) is a common, aggressive and poorly chemoresponsive subtype of DLBCL, characterized by constitutive canonical NF-κB signaling. Inhibition of NF-κB signaling leads to apoptosis of ABC-DLBCL cell lines, suggesting targeted disruption of this pathway may have therapeutic relevance. The selective IKK inhibitor, NEMO Binding Domain (NBD) peptide effectively blocks constitutive NF-κB activity and induces apoptosis in ABC-DLBCL cells in vitro. Here we used a comparative approach to determine the safety and efficacy of systemic NBD peptide to inhibit constitutive NF-κB signaling in privately owned dogs with spontaneous newly diagnosed or relapsed ABC-like DLBCL. Malignant lymph nodes biopsies were taken before and twenty-four hours after peptide administration to determine biological effects. Intravenous administration of <2 mg/kg NBD peptide was safe and inhibited constitutive canonical NF-κB activity in 6/10 dogs. Reductions in mitotic index and Cyclin D expression also occurred in a subset of dogs 24 hours post peptide and in 3 dogs marked, therapeutically beneficial histopathological changes were identified. Mild, grade 1 toxicities were noted in 3 dogs at the time of peptide administration and one dog developed transient subclinical hepatopathy. Long term toxicities were not identified. Pharmacokinetic data suggested rapid uptake of peptide into tissues. No significant hematological or biochemical toxicities were identified. Overall the results from this phase I study indicate that systemic administration of NBD peptide is safe and effectively blocks constitutive NF-κB signaling and reduces malignant B cell proliferation in a subset of dogs with ABC-like DLBCL. These results have potential translational relevance for human ABC-DLBCL.     

Cloning of the pig renal organic anion transporter 1 (pOAT1)

A pig kidney cDNA library was screened for the porcine ortholog of the multispecific organic anion transporter 1 (pOAT1). Several positive clones were isolated resulting in two alternatively spliced cDNA clones of pOAT1 (pOAT1 and pOAT1A). pOAT1-cDNAs consist of 2126 or 1895 base pairs (EMBL Acc. No. AJ308234 and AJ308235) encoding 547 or 533 amino acid residue proteins with 89, 87, 83 and 81% homology to the human, rabbit, rat, and mouse OAT1, respectively. Heterologous expression of pOAT1 in Xenopus laevis oocytes revealed an apparent K(m) for [3H]PAH of 3.75 +/- 1.6 microM. [3H]PAH uptake mediated by pOAT1 was abolished by 0.5 mM glutarate or 1 mM probenecid. Functional characterization of pOAT1A did not show any affinity for [3H]PAH. In summary, we cloned two alternative splice variants of the pig ortholog of organic anion transporter 1. One splice form (pOAT1) showed typical functional characteristics of organic anion transporter 1, whereas the second form appears not to transport PAH.     

Die Sonnenorientierung der V?gel. II. Entwicklung des Sonnenkompa? und sein Stellenwert im Orientierungssystem

Zusammenfassung Die vorliegende Arbeit versucht, die Sonnenorientierung der Vögel in ihrer Funktionsweise, ontogenetischen Entwicklung und biologischen Bedeutung nach dem heutigen Wissensstand darzustellen. Theoretisch kann die Sonne zur Bestimmung der Heimrichtung ( navigation), zum Aufsuchen einer als Kompaßrichtung bekannten Richtung und zum Einhalten der Richtung benutzt werden. Die meisten vorliegenden Befunde sprechen gegen eine Rolle der Sonne bei der Bestimmung der Heimrichtung nach Verfrachtung; die Funktion der Sonne als Sonnenkompaß und beim Richtungseinhalten ist dagegen durch zahlreiche Versuche bei verschiedenen Vogelarten gut belegt.Beim Aufsuchen einer Richtung mit dem Sonnenkompaß verrechnet der Vogel die Bewegung der Sonne auf ihrer scheinbaren Bahn, d. h. er schlägt einen tageszeitlich variablen Winkel zur Sonne ein, um in eine konstante Richtung zu fliegen. Dieser Winkel hängt allein von der inneren Uhr ab. Dabei scheint der Vogel im allgemeinen zu berücksichtigen, daß die Azimutwinkelgeschwindigkeit der Sonne gegen Mittag erheblich größer ist als in den frühen Vormittags- und späten Nachmittagsstunden.Untersuchungen bei Tauben ergaben, daß der Sonnenkompaß ein erlernter Orientierungsmechanismus ist: Sonnenazimut, Zeit und geographische Richtung werden aufgrund von Erfahrung miteinander in Beziehung gesetzt. Dabei muß die junge Taube die Sonne zu verschiedenen Tageszeiten beobachten, um den Sonnenkompaß während des ganzen Tages benutzen zu können. Der Zeitpunkt, zu dem der Sonnenkompaß gelernt wird, hängt stark von der Flugerfahrung der Tauben ab; er scheint sich zu entwickeln, sobald die Notwendigkeit, sich zu orientieren, auftritt, was normalerweise etwa gegen Ende des 3. Lebensmonats der Fall sein dürfte. Die Grundlagen und näheren Umstände des Lernprozesses sind noch weitgehend unbekannt.Versuche mit jungen Tauben sprechen dafür, daß der Sonnenkompaß bei der Entwicklung der Navigationsfähigkeit keine Rolle spielt; er scheint quasi nachträglich in das fertige Navigationssystem eingebaut zu werden. Dann aber stellt der Sonnenkompaß beim Heimfinden das bevorzugt benutzte Kompaßsystem dar, solange die Sonne zu sehen ist. Bei bedecktem Himmel kann er allerdings durch ein gleich leistungsfähiges nicht-visuelles System ersetzt werden.Bei tagziehenden jungen Zugvögeln — finnischen Staren — ließ sich eine Orientierung nach dem Sonnenkompaß noch nicht während des ersten Herbstzuges, sondern erst während des folgenden Frühjahrszuges nachweisen; allerdings ist unklar, inwieweit diese an handaufgezogenen Vögeln gewonnenen Befunde die natürlichen Verhältnisse widerspiegeln. Eine realistische Abschätzung der Bedeutung des Sonnenkompaß bei der Zugorientierung ist heute noch nicht möglich; theoretische überlegungen und die wenigen vorliegenden Befunde scheinen jedoch gegen eine Rolle des Sonnenkompaß als Referenzsystem für die angeborene Zugrichtung zu sprechen.

---

The sun orientation of birds

Summary In the present paper (part I: J. Orn. 121: 121–143, 1980), the sun orientation of birds, its way of functioning, ontogenetic development, and biological significance are described in the light of current experimental evidence. Theoretically, the sun can be used to determine which compass direction is the home direction ( true navigation), to set a compass course, and to maintain a given direction during flight. Most of the available evidence speaks against the sun's being used for determining the home direction after displacement, whereas many findings in several species of birds demonstrate use of the sun as a sun compass and for maintaining directions.Using the sun compass to go in a constant direction, the birds compensate for the sun's apparent movement, i. e. they fly at angles to the sun's azimuth direction which vary according to the time of day. The magnitude of these angles seems to depend on the birds' internal clock only, and the birds apparently consider the different rates of change of the sun's azimuth during the day (greater around noon than in early morning or late afternoon).Experiments with young homing pigeons show that the sun compass is not a completely innate orientation mechanism, but that the relation between sun azimuth, time and geographic direction is learned. A young pigeon must experience the sun at different hours of the day to establish a sun compass for the entire day. The age at which the sun compass is learned strongly depends on the bird's flying experience. The sun compass seems to be developed as soon as the bird encountered the necessity of orienting, which normally will be about the end of its third month. The details of the learning process are not yet known.The sun does not seem to be necessary for the development of the ability to navigate; in fact, some findings with young pigeons seem to indicate that the navigational system is already developed before the sun compass is added to it. Afterwards, however, the sun compass is used preferentially whenever the sun is visible. Under overcast skies, it is replaced by an equally effective non-visual system.In day-migrating birds — young Finnish starlings — sun compass orientation could not be demonstrated during the first autumn migration period, but the starlings were shown to use it during the following spring period. It is not clear, though, whether these data from handraised birds reflect the natural situation correctly. The available evidence does not yet allow a realistic estimate of the significance of the sun compass for orientation during migration; theoretical considerations and the few present data, however, make it appear improbable that the sun compass acts as a reference system for the innate migratory direction.

     

Grazing, social and comfort behaviour of Ankole and crossbred (Ankole × Holstein) heifers on pasture in south western Uganda

The aim of this study was to assess the grazing, social and comfort behaviour of the indigenous purebred Ankole cattle breed and crossbred (Holstein × Ankole) animals under typical management conditions in south western Uganda. Twelve focal animals in each of four groups (two groups per genotype) were observed regarding their grazing, social and comfort behaviour on pasture.No significant differences in grazing behaviour patterns (eating, walking, standing) were found between the genotypes. Resting occurred only very rarely in both genotypes. Walking distances of Ankole and Ankole × Holstein crosses were also similar. There was no difference in the occurrence of agonistic interactions between the two genotypes. However, Ankole cattle engaged in more non-agonistic social interactions than their crossbred counterparts. Individual distances were lower in Ankole heifers and more herd mates were found within a radius of 5 m around the Ankole animals. The most important comfort behaviour pattern in both genotypes was self-licking, which occurred to similar frequency in Ankole and crossbred heifer groups. Crossbred animals scratched themselves and rubbed on objects more often than Ankole heifers.Although Ankole cattle and their Holstein crosses did not differ in grazing, distances walked and agonistic behaviours, the significant differences between the two genotypes in herd cohesion and comfort behaviour may pose challenges on the management of crossbred animals under extensive open grazing conditions as present in south western Uganda. Thus, apart from (re)productive performance traits, behavioural traits of both genotypes may also be taken into account for breeding decisions and management under current production conditions.     

Allogeneic tumor lysate can serve as both antigen source and protein supplementation for dendritic cell culture

BACKGROUND: Recent preclinical and clinical evidence suggests the use of allogeneic tumor as a source of antigen for DC-based immunotherapy against cancer. We hypothesized that addition of allogeneic tumor lysate to monocyte-derived DC culture could serve a dual purpose: (1) antigen source and (2) protein supplementation of DC culture media. Protein supplementation whether of known origin (human serum/plasma, fetal bovine serum, human serum albumin) or undeclared origin ("serum-free" media) is a source of variability and bias. We addressed the question whether protein supplementation can be omitted in the presence of allogeneic tumor lysate. MATERIALS AND METHODS: Human DC cultured in the presence of lysate from medullary thyroid carcinoma (MTC) cell line SHER-I (TuLy-DC) and DC pulsed with the same lysate but cultured in the presence of FBS (FBS-DC) were assessed for morphology, phenotype, maturation and functional properties. RESULTS: In comparison of FBS-DC/TuLy-DC no significant differences in morphology, phenotype and maturation could be detected. Both culture conditions produced CD1a(high), CD14(low) DC with high expression of costimulatory molecules and CD83 upon stimulation. TuLy-DC gave significantly better yields and produced more IL12p70. DC showed high (allo)stimulatory capacity toward T-cells. TuLy-DC induced more intracellular IFNgamma in CD8+T-cells of vaccinated MTC patients. Both types of DC induced killing of SHER-I after short in vitro restimulation. Tumor lysate from SHER-I can substitute for further protein supplementation in DC culture. Allogeneic tumor lysates should be taken into consideration as both source of antigen and protein supplementation in monocyte-derived DC culture.