Serum antibodies to Escherichia coli in breast-fed and bottle-fed infants.

Titers of antibody against Escherichia coli in human milk and in the sera of 11 breast-fed infants, 6 bottle-fed infants and 9 infants in the post-weaning period were measured by the passive hemagglutination method. High antibody titers were observed in human milk in the first 4 days after parturition, but the titer decreased rapidly thereafter. None of the healthy, breast-fed infants had detectable serum antibodies, while a breast-fed infant with a perianal E. coli abscess had antibodies. On the other hand, 4 of the 6 bottle-fed infants and all of the 9 infants in the post-weaning period had antibodies. The significance of these results was discussed.</p

ND:YVO4ナノ秒レーザーを使用したジルコニアコーピングの新しい加工法

The purpose of this work was to fabricate zirconia copings from fully sintered Y-TZP blocks using a Nd:YVO4 nanosecond laser in order to avoid complicated procedures using conventional CAD/CAM systems. To determine the most appropriate power level of a Nd:YVO4 laser, cuboid fully sintered Y-TZP specimens were irradiated at six different average power levels. One-way ANOVAs for the average surface roughness and laser machining depth revealed that an average power level of 7.5 W generated a smooth machined surface with high machining efficiency. Y-TZP copings were then machined using the proposed method with the most appropriate power level. As the number of machining iterations increased, the convergence angles decreased significantly (p<0.01). The accuracy of the machined copings was judged to be good based on 3D measurements and traditional metal die methods. The proposed method using the nanosecond laser was demonstrated to be useful for fabricating copings from fully sintered Y-TZP.日本歯科大学201

Contributing Processes to Arctic Temperature Amplification for a Range of Forcing in MIROC GCM

第3回極域科学シンポジウム/第35回極域気水圏シンポジウム 11月30日（金） 国立国語研究所 ２階多目的

Casting of MOD inlay using rings with holes on both sides : 12～18 wt%Au-20～26Pd-14.48～26.48Cu-40Ag-1.57Zn-0.02Ir alloys

Using a casting ring with openings on both sides and a water-absorbent polymer, heterogeneity is maintained in a single casting and a precise MOD inlay can be produced. We produced 9 different kinds of gold-silver-palladium (Au-Ag-Pd) alloys by changing the ratio of palladium, gold, and copper and investing them, and changing parameters such as the angulation of the casting ring openings and the water:powder ratios to produce MOD inlay castings. We measured the expansion and shrinkage percentage of the castings in both the buccolingual and mesiodistal directions. From this experiment, we learned that precise MOD inlay castings can be produced using rings with 240° openings when invested in a thick mix having a standard water:powder ratio or using rings with 200° openings when invested in a thick mix having a water:powder ratio for a 12wt%Au-20〜26Pd-20.48〜26.48Cu-40Ag-1.5Zn-0.02Ir alloy

Identification of hypoxia-inducible factor 1 ancillary sequence and its function in vascular endothelial growth factor gene induction by hypoxia and nitric oxide.

Transcription of hypoxia-inducible genes is regulated by hypoxia response elements (HREs) located in either the promoter or enhancer regions. Analysis of these elements reveals the presence of one or more binding sites for hypoxia-inducible factor 1 (HIF-1). Hypoxia-inducible genes include vascular endothelial growth factor (VEGF), erythropoietin, and glycolytic enzyme genes. Site-directed mutational analysis of the VEGF gene promoter revealed that an HIF-1 binding site (HBS) and its downstream HIF-1 ancillary sequence (HAS) within the HRE are required as cis-elements for the transcriptional activation of VEGF by either hypoxia or nitric oxide (NO). The core sequences of the HBS and the HAS were determined as TACGTG and CAGGT, respectively. These elements form an imperfect inverted repeat, and the spacing between these motifs is crucial for activity of the promoter. Gel shift assays demonstrate that as yet unknown protein complexes constitutively bind to the HAS regardless of the presence of these stimuli in several cell lines, in contrast with hypoxia- or NO-induced activation of HIF-1 binding to the HBS. A common structure of the HRE, which consists of the HBS and the HAS, is seen among several hypoxia-inducible genes, suggesting the presence of a novel mechanism mediated by the HAS for the regulation of these genes

Activator protein-1 responsive to the group II metabotropic glutamate receptor subtype in association with intracellular calcium in cultured rat cortical neurons

金沢大学大学院自然科学研究科分子作用学Activation of ionotropic glutamate (Glu) receptors, such as N-methyl-d-aspartate receptors, is shown to modulate the gene transcription mediated by the transcription factor activator protein-1 (AP1) composed of Fos and Jun family proteins in the brain, while little attention has been paid to the modulation of AP1 expression by metabotropic Glu receptors (mGluRs). In cultured rat cortical neurons, where constitutive expression was seen with all groups I, II and III mGluR subtypes, a significant and selective increase was seen in the DNA binding activity of AP1 120 min after the brief exposure to the group II mGluR agonist (2S,2′R,3′R)-2-(2′,3′-dicarboxycyclopropyl)glycine (DCG-IV) for 5 min. In cultured rat cortical astrocytes, by contrast, a significant increase was induced by a group I mGluR agonist, but not by either a group II or III mGluR agonist. The increase by DCG-IV was significantly prevented by a group II mGluR antagonist as well as by either an intracellular Ca2+ chelator or a voltage-sensitive Ca2+ channel blocker, but not by an intracellular Ca2+ store inhibitor. Moreover, DCG-IV significantly prevented the increase of cAMP formation by forskolin in cultured neurons. Western blot analysis revealed differential expression profiles of Fos family members in neurons briefly exposed to DCG-IV and NMDA. Prior or simultaneous exposure to DCG-IV led to significant protection against neuronal cell death by NMDA. These results suggest that activation of the group II mGluR subtype would modulate the gene expression mediated by AP1 through increased intracellular Ca2+ levels in cultured rat cortical neurons. © 2007