Effective dose equivalent on the ninth Shuttle--Mir mission (STS-91)

Organ and tissue doses and effective dose equivalent were measured using a life-size human phantom on the ninth Shuttle-Mir Mission (STS-91, June 1998), a 9.8-day spaceflight at low-Earth orbit (about 400 km in altitude and 51.65 degrees in inclination). The doses were measured at 59 positions using a combination of thermoluminescent dosimeters of Mg(2)SiO(4):Tb (TDMS) and plastic nuclear track detectors (PNTD). In correcting the change in efficiency of the TDMS, it was assumed that reduction of efficiency is attributed predominantly to HZE particles with energy greater than 100 MeV nucleon(-1). A conservative calibration curve was chosen for determining LET from the PNTD track-formation sensitivities. The organ and tissue absorbed doses during the mission ranged from 1.7 to 2.7 mGy and varied by a factor of 1.6. The dose equivalent ranged from 3.4 to 5.2 mSv and varied by a factor of 1.5 on the basis of the dependence of Q on LET in the 1990 recommendations of the ICRP. The effective quality factor (Q(e)) varied from 1.7 to 2.4. The dose equivalents for several radiation-sensitive organs, such as the stomach, lung, gonad and breast, were not significantly different from the skin dose equivalent (H(skin)). The effective dose equivalent was evaluated as 4.1 mSv, which was about 90% of the H(skin).     

On the parameter describing the generalised equivalent uniform dose (gEUD) for tumours

The purpose of the present work was to estimate the parameter ‘a’ describing the generalised equivalent uniform dose (gEUD) for tumours and its dependence on radiobiological parameters. The consequences of uncertainties in a on the gEUD were also studied. An estimate of a was found by requiring that, for a given target dose distribution, the mechanistic EUD (based on radiobiological linear quadratic modelling) equals gEUD. The estimate of a was found to depend on the dose distribution, and decreased with factors that increase the slope of the cell survival curve (i.e. decreasing α/β values and increasing α values). Furthermore, the parameter a was estimated for 35 prostate cancer IMRT plans of varying dose distributions, for two sets of previously published radiobiological parameters: (1) α = 0.15 Gy⁻¹ and α/β = 3 Gy, and (2) α = 0.26 Gy⁻¹ and α/β = 10 Gy. The estimated values of a ranged from −25.6 to −22.4 for all combinations of dose distributions and parameter sets. Uncertainties in a were found to give only small uncertainties in gEUD. Although the current work shows limitations of the gEUD model for tumours, gEUD may still be preferable for biological treatment plan optimization, evaluation and reporting.     

Structural Basis for Homodimerization of the Src-associated during Mitosis, 68-kDa Protein (Sam68) Qua1 Domain

Sam68 (Src-associated during mitosis, 68 kDa) is a prototypical member of the STAR (signal transducer and activator of RNA) family of RNA-binding proteins. STAR proteins bind mRNA targets and modulate cellular processes such as cell cycle regulation and tissue development in response to extracellular signals. Sam68 has been shown to modulate alternative splicing of the pre-mRNAs of CD44 and Bcl-xL, which are linked to tumor progression and apoptosis. Sam68 and other STAR proteins recognize bipartite RNA sequences and are thought to function as homodimers. However, the structural and functional roles of the self-association are not known. Here, we present the solution structure of the Sam68 Qua1 homodimerization domain. Each monomer consists of two antiparallel α-helices connected by a short loop. The two subunits are arranged perpendicular to each other in an unusual four-helix topology. Mutational analysis of Sam68 in vitro and in a cell-based assay revealed that the Qua1 domain and residues within the dimerization interface are essential for alternative splicing of a CD44 minigene. Together, our results indicate that the Qua1 homodimerization domain is required for regulation of alternative splicing by Sam68.     

Energetic equivalent of the production of plasma lactate during running of supramaximal intensity

The energy equivalent of plasma lactate production (ELAp) represents the amount of energy that can be derived from the anaerobic glycolysis per kg body weight when the peak plasma lactate concentration (LAp) after exercise increases by 1 mM. ELAp has been calculated from the relationship between the oxygen deficit (Do2) and LAp in 32 subjects. LAp and oxygen uptake measurements were made during constant speed supramaximal running until exhaustion or during the course of constant-speed supramaximal runs of different duration interrupted by 8- to 10- min resting periods. The relationship between Do2 and LAp is described by a linear equation where the slope is equal to ELAp. This equation is: Do2 = 12.3 + 2.4 LAp (r = 0.958; P less than 0.001), where Do2 is expressed in ml O2/kg and LAp in mmol/litre (mM). These findings validate LAp measurements as an index of the anaerobic metabolism during supramaximal running.     

Serum amyloid-A (SAA) and haptoglobin (Hp) plasma concentrations in newborn calves

The concentrations of 2 major bovine acute-phase proteins, haptoglobin (Hp) and serum amyloid-A (SAA), were measured in plasma obtained shortly after birth from 22 healthy calves. In a separate group of diseased calves (n = 8), Hp and SAA concentrations were measured to determine whether newborn calves (up to 4 d old) are able to produce SAA and Hp. In blood samples taken directly after birth, the Hp plasma concentrations were all below the limit of detection. The mean SAA concentration was independent of weight (r = 0.063), degree of acidosis (r = -0.125), sex (p > 0.05), and were not different in calves born after different types of obstetrical help (p > 0.05). In the group of diseased calves, an increased Hp concentration was measured in only 2 of 8 animals, whereas the mean SAA concentration was significantly higher (p < 0.05) than in the healthy newborn calves. These data suggest that prenatal stress due to parturition does not form a stimulus for the production of acute-phase proteins in the fetal calf. The low Hp plasma concentrations might indicate that either it takes a few days to establish a detectable concentration of this protein, or that Hp production is not fully developed in newborn calves.     

Channel-forming (Porin) activity in Herpetosiphon aurantiacus Hp a2

Detergent extracts of cell envelopes of the gliding bacterium Herpetosiphon aurantiacus formed channels in lipid bilayers. Fast protein liquid chromatography across a HiTrap-Q cation-exchange column demonstrated that a 45-kDa protein forms the channel. The observation of a channel-forming protein suggests that Herpetosiphon aurantiacus Hp a2 has a permeability barrier on its surface.     

Monte Carlo simulation of neutron dose equivalent by photoneutron production inside the primary barriers of a radiotherapy vault

PurposeTo evaluate the neutron dose equivalent produced by photoneutrons inside the primary barriers of a radiotherapy vault.MethodsMonte Carlo simulations were performed for investigating the production of photoneutrons as well as neutron shielding requirements. Two photon beams of 15 and 18 MV struck sheets of steel and lead, and the neutron doses were calculated at the isocenter (P_iso) and at a distance of 50 cm from the inside wall (P_wall) while delivering 1 Gy to the patient. The proper thicknesses of borated polyethylene (BPE) and concrete were simulated to reduce neutron contamination.ResultsWhen the primary barrier consisted of a concrete alone, the neutron doses at P_iso were 0.5 μSv/Gy and 12.8 μSv/Gy for 15- and 18-MV, respectively. At P_wall, the neutron doses were 15.8 μSv/Gy and 318.4 μSv/Gy for 15- and 18-MV, respectively. When 15 MV photons interacted with metal sheets, the neutron doses were 0.4–22.2 μSv/Gy at P_iso and 15.8–812.5 μSv/Gy at P_wall, depending on the thickness and material of the metal sheets and neutron shielding. In the case of 18 MV photons with the same configuration, the neutron doses were 0.9–59.5 μSv/Gy and 73.9–5006.1 μSv/Gy for P_iso and P_wall, respectively. The neutron dose delivered to the patient was reduced to the level of the dose delivered with a concrete barrier by including a 10-cm-thick BPE for each beam.ConclusionsWhen the primary barrier shielding is designed with a metal sheet inside for high energy, proper neutron shielding should be constructed to avoid undesirable photoneutron dose.     

Ultrasound production during stridulation by hydropsychid larvae (Trichoptera)

The stridulatory apparatus of eight species of 5th instar caddis larvae of the family Hydropsychidae were compared using the scanning electron microscope. This revealed the presence of secondary structures associated with each main ridge of the file in some species. Slight differences occur in the number of ridges which form the plectra. The sounds produced by two coexisting species of hydropsychid larvae were recorded and temporal and frequency analysis carried out. These sounds are found to extend far into the ultrasonic range and appear to show only minor interspecific differences. The occurrence of stridulatory behaviour during territorial defence and its significance in relation to the ecology of the larvae is discussed. Some physical parameters affecting sound reception in the near- and far-field are presented and this leads to speculation on the existence of a possible hearing mechanism.     

The 68-kDa Telomeric Repeat Binding Factor 1 (TRF1)-associated Protein (TAP68) Interacts with and Recruits TRF1 to the Spindle Pole during Mitosis

The telomere capping protein TRF1 is a component of the multiprotein complex “shelterin,” which organizes the telomere into a high order structure. Besides telomere maintenance, telomere-associated proteins also have nontelomeric functions. For example, tankyrase 1 and TRF1 are required for the maintenance of faithful mitotic progression. However, the functional relevance of their centrosomal localization has not been established. Here, we report the identification of a TRF1-binding protein, TAP68, that interacts with TRF1 in mitotic cells. TAP68 contains two coiled-coil domains and a structural maintenance of chromosome motifs and co-localizes with TRF1 to telomeres during interphase. Immediately after nuclear envelope breakdown, TAP68 translocates toward the spindle poles followed by TRF1. Dissociation of TAP68 from the telomere is concurrent with the Nek2A-dependent phosphorylation at Thr-221. Biochemical characterization demonstrated that the first coiled-coil domain of TAP68 binds and recruits TRF1 to the centrosome. Inhibition of TAP68 expression by siRNA blocked the localization of TRF1 and tankyrase 1 to the centrosome. Furthermore, siRNA-mediated depletion of TAP68 perturbed faithful chromosome segregation and genomic stability. These findings suggest that TAP68 functions in mediating TRF1-tankyrase 1 localization to the centrosome and in mitotic regulation.     

鼠γ疱疹病毒68(MHV68):研究γ疱疹病毒感染的模型

γ疱疹病毒成员遍及自然界,可感染包括人在内的多种哺乳动物.γ疱疹病毒的生物学特性主要有:(1)能在淋巴细胞中潜伏感染;(2)可以产生淋巴增生性疾病;(3)与淋巴组织和非淋巴组织肿瘤关系密切.最开始γ疱疹病毒根据感染T或B细胞的不同而分为γ1和γ2疱疹病毒,前者主要感染B淋巴细胞,如感染人和棉顶绒猴的EBV(EpsteinBarr virus);γ2疱疹病毒则感染T淋巴细胞,以感染松鼠猴的疱疹病毒samiri(herpesvirus samiri,HVS)为代表.但后来证实γ2疱疹病毒可同时感染T、B淋巴细胞,而EBV亦可引起T淋巴细胞肿瘤.因此以后发现的γ疱疹病毒则根据其基因结构及基因组中代表性序列的特点,将其归为γ1或γ2亚类.如感染人的卡波氏肉瘤相关病毒(Kaposi's sarcomaassociated herpesvirus,KSHV)或称人疱疹病毒8(human herpesvirus-8,HHV8)就归为γ2[1].     

Changes in androgen binding protein (ABP) production following continuous low dose gamma irradiation (IR) of adult rat

Continuous low dose gamma irradiation induces a progressive degeneration of germ cells with a concomittant increase in blood FSH; however, the Sertoli cell function is not too much altered since serum ABP level is normal and it is likely that the decrease of epididymal ABP content is the consequence of a reduction in seminiferous tubule fluid excretion. Obviously, spermatids seems to be involved in the regulation of Sertoli cell ABP synthesis.     

The genetics of stamenoid petal production in oilseed rape (Brassica napus) and equivalent variation in Arabidopsis thaliana

 The agronomic potential of a Brassica napus variant with petalless flowers was compromised by an associated detrimental change in leaf morphology. Genetic analysis demonstrated the cosegregation of genes controlling both morphologies. Two STAP loci controlling the production of flowers with stamenoid petals were mapped to homoeologous locations in the genome of B. napus. The STAP loci were probably duplicate genes because they exhibited an epistatic interaction such that only plants homozygous for recessive stap alleles at both loci expressed the variant phenotype. The CURLY LEAF (CLF) gene of Arabidopsis thaliana pleiotropically influences both flower and leaf morphologies. The cloned CLF gene of Arabidopsis was homologous to a polymorphic B. napus locus coincident with one of the B. napus STAP loci. The possibility that CLF is a candidate gene for STAP suggests that the variant stap alleles of B. napus exert pleiotropic effects over both flower and leaf morphologies. Received: 26 August 1996 / Accepted: 20 September 1996     

Fertilizer and manure equivalent rates on forage corn production (<i>Zea mays</i>)

An experiment with increasing rates of fertilizer and manure in silage corn was established to evaluate the agronomic crop response and to estimate the manure nitrogen availability. The treatments were designed to deliver 0, 67, 100 and 133% of the crop nitrogen requirements (CNR), using ammonium sulphate and manure as N source. Dry matter (DM) yield was similar among treatments receiving N, but those values were greater than those found in the control. Nitrogen extraction at harvest was not statistically different in treatments with fertilizer or manure, but it was higher in these treatments than in the control without N (p≤ 0.05). With both sources of N, crop N extraction was adjusted to a quadratic regression equation, as a function of N rates. According to the fertilizer equivalence (EF) methodology, the rate of 231.3 kg/ha of inorganic fertilizer N, and 752.9 kg/ha of total N in manure, had 129.5 kg/ha of N extracted by the crop. The ratio of the above rates, fertilizer N/ manure total N, represents the crop available manure N; in the present study, it was 30.7% of total N in the manure. Since no differences in yield were observed between N sources, it is concluded that N fertilizer can be substituted by manure, at a rate estimated to provide the crop N requirements. The estimation of the manure available N is important to adjust manure rates, thereafter avoiding excessive applications and pollution risks.