Lens spaces obtainable by surgery on doubly primitive knots

In this paper, we consider which lens spaces are obtainable by Dehn surgery described by Berge on doubly primitive knots. It is given an algorithm to decide whether a given lens space is obtainable by such surgery. Also included is a complete characterization of such surgery yielding lens spaces with Klein bottles.Comment: 9 pages, 8 figure

Site specific regulation in the kidney of endothelin and its receptor subtypes by cyclosporine

Site selective regulation in the kidney of endothelin and its receptor subtypes by cyclosporine. Endothelin (Et) has been suggested by us and others to play a role in glomerular dysfunction that characterizes cyclosporine (Cs)-associated nephrotoxicity. Since Et exerts its actions through at least two receptor subtypes, and because these receptor subtypes have particular distributions in the renal parenchyma, we investigated changes in mRNA expression for Et and its receptor subtypes in glomeruli and medulla of rats treated with Cs. Polymerase chain reaction coupled with reverse transcription (RT-PCR) method was used to assess prepro-Et-1, type A (EtA) and type B (EtB) receptor mRNA at 1, 3, 6, and 24 hours after Cs (20 mg/kg body wt i.v.). Results were normalized to the expression of β-actin as an internal standard. Compared with control rats, glomerular mRNA expression for prepro-Et-1 was not affected by Cs. Similarly, Cs did not significantly change the glomerular mRNA expression of either EtA or EtB receptor subtypes. By contrast, in the medulla there was a marked and persistent increase in the expression for prepro-Et-1 and the EtB receptor subtype: prepro-Et-1 at 1, 3, 6, and 24 hours was 336 ± 61, 295 ± 65, 339 ± 73,440 ± 123% of controls, respectively (P < 0.05 compared with controls at each time point). The EtB receptor mRNA at 1, 3, 6, 24 hours was 164 ± 22, 157 ± 15, 148 ± 14, 116 ± 18% (compared with controls, P < 0.01 at 3hr and P < 0.05 at 1 and 6 hr), while the mRNA expression for EtA was not affected by Cs treatment. These results demonstrate that, in vivo, Cs selectively modulates renal mRNA expression for Et peptide and one of its receptor subtypes. Furthermore, the modulation is site specific. These changes are most conspicuous in the renal medulla, such that mRNA expression for prepro-Et-1 and EtB increases and remains elevated for at least six hours after Cs administration. These alterations may contribute to the vasospastic as well as proliferative abnormalities which characterize Cs nephrotoxicity

Oxidants induce transcriptional activation of manganese superoxide dismutase in glomerular cells

Oxidants induce transcriptional activation of manganese superoxide dismutase in glomerular cells. Cultured rat glomerular mesangial and epithelial cells and bovine glomerular endothelial cells were exposed to various concentrations of hydrogen peroxide (H2O2). Mesangial cells treated with 10 to 100 µM H2O2 for 24 hours showed a two- to ninefold increase in Mn-SOD mRNA expression associated with significantly (P < 0.005) increased Mn-SOD activity (22.2 ± 1.2 and 12.2 ± 0.7 µ/mg protein for H2O2 100 µM treated and untreated cells, respectively). In contrast, expression of Cu-Zn SOD and β-actin mRNA was not affected by H2O2. Induction of Mn-SOD mRNA by H2O2 was inhibited by actinomycin-D (4 µM) treatment. Glomerular endothelial cells also showed an increase in Mn-SOD mRNA expression following 100 µM H2O2 treatment, as did glomerular epithelial cells following treatment with 500 and 1000 µM H2O2 but not with 100 µM. Transcriptional activity of the Mn-SOD gene was assessed with a fusion reporter gene consisting of a luciferase gene (pGL2P) and a 1.2 kb fragment from the rat Mn-SOD genomic DNA (-806 to +408 bp of the transcription initiation site, -806:+408). The construct was transfected into rat glomerular mesangial and epithelial cells. Mesangial and epithelial cells transfected with pGL2P (-806:+408) and treated with H2O2 (100 µM and 1 mM for mesangial and epithelial cells, respectively) demonstrated some threefold increase in luciferase activity, whereas cells transfected with pGL2P lacking the Mn-SOD fragment did not show changes in luciferase activity following H2O2 treatment. Other oxidants, namely α- and β-naphthoflavone (50 µM to mesangial cells) and puromycin aminonucleoside (25 to 50 µg/ml to epithelial cells), also induced transcriptional activation (2- to 5-fold increase) in these cells. Thus, Mn-SOD levels in glomerular cells are enhanced when they are exposed to oxidant stress, and this up-regulation involves transcriptional activation. Further, the Mn-SOD gene contains enhancer element(s) which respond to diverse oxidant stress. The inducibility by oxidants of local Mn-SOD demonstrates that glomerular SOD may play a decisive role in the pathogenesis of glomerular injuries in which the balance between oxidants and antioxidants is critical

Original Article

Tetrodotoxin, a toxic substance obtained from the globe fish, has been known to paralise the neuromuscular system as well as the central nervous system and recently, it was found to block production of the action potential through its selective inhibition of the sodium-carrying mechanism, but has no effect on the resting potential. In this paper, the effects of tetrodotoxin on the four kinds of skeletal muscle fibers were compared and analysed. Four muscle fibers are tonic and phasic fibers of the extrafusal muscle, and nuclear-bag and nuclear-chain fibers of the intrafusal muscle fibers. The extrafusal muscle is a dynamic source of posture and locomotion, the intrafusal muscle being the regulating source of them. Paralysis of the extrafusal muscle fibers was determined by measuring the decrease in maximum contraction of the soleus (tonic muscle) and tibialis anterior (phasic) produced stimulation of the distal cut end of the ventral root. Paralysis of the intrafusal muscle fibers wasmeasured by a change in the frequency of Group la discharge led from the functionally isolated single filaments of the distal cut end of the dorsal root. By intravenous administration of 4γ/kg tetrodotoxin, paralysis advaces beginning with the intrafusal muscle fibers, and then on to the tonic muscle and phasic muscle fibers. They recover according to the same order. When the intrafusal muscle fiber recovers during an advance in paralysis of the extrafusal muscle, intrafusal muscle fibers contract by the γ-efferent activated by stimulation of the ventral root, and the Group la discharge increases. Frequency of the Group la discharge increases in proportion to muscle extension, therefore the contraction curve of the intrafusal muscle fiber is measured from augmentation of the discharge frequency. Contraction of the intrafusal muscle fibers lasts for several hundred msec, and the curve has two peaks at about 60 msec, and 110 (Fig. 5).It is clear then that the former corresponds to contraction of the nuclear-bag fiber, and the latter to contraction of the nuclearchain fiber

Gastric T-cell lymphoma associated with hemophagocytic syndrome

BACKGROUND: Lymphoma-associated hemophagocytic syndrome (LAHS) occurs in mostly extra nodal non-Hodgkin's lymphoma. LAHS arising from gastrointestinal lymphoma has never been reported. Here we report a case of gastric T-cell lymphoma-associated hemophagocytic syndrome. CASE PRESENTATION: A 51-year-old woman presented with pain, redness of breasts, fever and hematemesis. Hematological examination revealed anemia. Gastroscopy revealed small bleeding ulcers in the stomach and the computed tomography scan showed liver tumor. She underwent total gastrectomy for gastrointestinal bleeding and the histopathology revealed gastric T-cell lymphoma. She continued to bleed from the anastomosis and died on the 8th postoperative day. Autopsy revealed it to be a LAHS. CONCLUSIONS: If Hemophagocytic syndrome (HPS) occurs in lymphoma of the gastrointestinal tract, bleeding from the primary lesion might be uncontrollable. Early diagnosis and appropriate treatment are needed for long-term survival

Mechanical Characterization of One-Headed Myosin-V Using Optical Tweezers

Class V myosin (myosin-V) is a cargo transporter that moves along an actin filament with large (∼36-nm) successive steps. It consists of two heads that each includes a motor domain and a long (23 nm) neck domain. One of the more popular models describing these steps, the hand-over-hand model, assumes the two-headed structure is imperative. However, we previously succeeded in observing successive large steps by one-headed myosin-V upon optimizing the angle of the acto-myosin interaction. In addition, it was reported that wild type myosin-VI and myosin-IX, both one-headed myosins, can also generate successive large steps. Here, we describe the mechanical properties (stepsize and stepping kinetics) of successive large steps by one-headed and two-headed myosin-Vs. This study shows that the stepsize and stepping kinetics of one-headed myosin-V are very similar to those of the two-headed one. However, there was a difference with regards to stability against load and the number of multisteps. One-headed myosin-V also showed unidirectional movement that like two-headed myosin-V required 3.5 kBT from ATP hydrolysis. This value is also similar to that of smooth muscle myosin-II, a non-processive motor, suggesting the myosin family uses a common mechanism for stepping regardless of the steps being processive or non-processive. In this present paper, we conclude that one-headed myosin-V can produce successive large steps without following the hand-over-hand mechanism

Feeding effect of selenium enriched rotifers on larval growth and development in red sea bream Pagrus major

Feeding trials were conducted to investigate the effect of selenium (Se)-enriched rotifers on growth and development of red sea bream Pagrus major larvae. Fish were reared from fertilized eggs (98% hatch rate) to 20. days post hatch (dph) at 19. °C with two different food sources; non-enriched S-type rotifers (0.0. μg. Se/g D.W., control diet) or Se-enriched rotifers (2.2. μg. Se/g D.W., Se-enriched diet) at 10. rotifers/mL, respectively. On the last day of larviculture, the Se-enriched diet accelerated growth and developmental stage of fish larvae. The larvae fed Se-enriched rotifers were advanced in the following parameters compared to those fed control diet: total length (6.06 vs 5.53. mm), standard length (5.74 vs 5.26. mm), head length (1.46 vs 1.28. mm), eye diameter (0.57 vs 0.50. mm), the number of caudal fin rays (5.8 vs 1.9), and the proportion of individuals undergoing notochord flexion (55 vs 3%). Fish larvae of 20. dph showed higher Se concentration (9.5 ± 0.2. μg/g DW) with the Se-enriched diet than with the control diet (1.3 ± 0.3. μg/g DW), but there were no significant differences in the composition of polyunsaturated fatty acids which significantly affect larval growth and development. Therefore, the feeding of Se enriched rotifers enhanced growth and development of the red sea bream P. major larvae

Integrative Annotation of 21,037 Human Genes Validated by Full-Length cDNA Clones

The human genome sequence defines our inherent biological potential; the realization of the biology encoded therein requires knowledge of the function of each gene. Currently, our knowledge in this area is still limited. Several lines of investigation have been used to elucidate the structure and function of the genes in the human genome. Even so, gene prediction remains a difficult task, as the varieties of transcripts of a gene may vary to a great extent. We thus performed an exhaustive integrative characterization of 41,118 full-length cDNAs that capture the gene transcripts as complete functional cassettes, providing an unequivocal report of structural and functional diversity at the gene level. Our international collaboration has validated 21,037 human gene candidates by analysis of high-quality full-length cDNA clones through curation using unified criteria. This led to the identification of 5,155 new gene candidates. It also manifested the most reliable way to control the quality of the cDNA clones. We have developed a human gene database, called the H-Invitational Database (H-InvDB; http://www.h-invitational.jp/). It provides the following: integrative annotation of human genes, description of gene structures, details of novel alternative splicing isoforms, non-protein-coding RNAs, functional domains, subcellular localizations, metabolic pathways, predictions of protein three-dimensional structure, mapping of known single nucleotide polymorphisms (SNPs), identification of polymorphic microsatellite repeats within human genes, and comparative results with mouse full-length cDNAs. The H-InvDB analysis has shown that up to 4% of the human genome sequence (National Center for Biotechnology Information build 34 assembly) may contain misassembled or missing regions. We found that 6.5% of the human gene candidates (1,377 loci) did not have a good protein-coding open reading frame, of which 296 loci are strong candidates for non-protein-coding RNA genes. In addition, among 72,027 uniquely mapped SNPs and insertions/deletions localized within human genes, 13,215 nonsynonymous SNPs, 315 nonsense SNPs, and 452 indels occurred in coding regions. Together with 25 polymorphic microsatellite repeats present in coding regions, they may alter protein structure, causing phenotypic effects or resulting in disease. The H-InvDB platform represents a substantial contribution to resources needed for the exploration of human biology and pathology