スイ カセイ ノウホウ ニ タイスル フククウキョウカ ノホウ イ フンゴウジュツ : イヘキ トノ ユチャク オ ゼンテイ ト シナイ アンゼンナ ジュツシキ

A forty seven-year-old male who had been in clinical follow-up for a pancreatic pseudocystunderwent a laparoscopic cystogastrostomy through the lesser peritoneal sac in 1996. Thisprocedure is performed by creating a cystotomy and posterior gastrotomy through whichan Endo GIATM is applied. The mouth of cystogastrostomy is closed using continuous suturesby Endo STITCHTM. This approach does not rely on adhesions between the pseudocyst andposterior wall of the stomach, and offers clear advantages over previously described techniquesin the management of pancreatic pseudocyst

A role for fungal β-glucans and their receptor Dectin-1 in the induction of autoimmune arthritis in genetically susceptible mice

A combination of genetic and environmental factors can cause autoimmune disease in animals. SKG mice, which are genetically prone to develop autoimmune arthritis, fail to develop the disease under a microbially clean condition, despite active thymic production of arthritogenic autoimmune T cells and their persistence in the periphery. However, in the clean environment, a single intraperitoneal injection of zymosan, a crude fungal β-glucan, or purified β-glucans such as curdlan and laminarin can trigger severe chronic arthritis in SKG mice, but only transient arthritis in normal mice. Blockade of Dectin-1, a major β-glucan receptor, can prevent SKG arthritis triggered by β-glucans, which strongly activate dendritic cells in vitro in a Dectin-1–dependent but Toll-like receptor-independent manner. Furthermore, antibiotic treatment against fungi can prevent SKG arthritis in an arthritis-prone microbial environment. Multiple injections of polyinosinic-polycytidylic acid double-stranded RNA also elicit mild arthritis in SKG mice. Thus, specific microbes, including fungi and viruses, may evoke autoimmune arthritis such as rheumatoid arthritis by stimulating innate immunity in individuals who harbor potentially arthritogenic autoimmune T cells as a result of genetic anomalies or variations

In Situ Probing of Photoinduced Hydrophilicity on Titania Surface Using Dye Molecules

The titania film surface exhibits superhydrophilicity after UV irradiation due to its photocatalytic function. This is caused by a change in the density of the surface hydroxyl groups, which affects the surface charge density. Titania films were prepared to observe the change in the surface charge during UV irradiation. The amounts of some xanthene dyes adsorbed and deposited on the titania films after UV irradiation were evaluated as a function of the irradiation time. The increase in the adsorption and deposition amounts of the more negative dye versus the UV irradiation time was greater. These results indicated that the titania surface charge became more positive by the UV irradiation. It was reported that basic hydroxyl groups formed on the titania particle surface during the UV irradiation. The surface dissociates hydroxyl ions into the water phase and has a positive charge, which was supported by the present study

Novel and Efficient Chromium(II)-Mediated Desulfonylation of α‑Sulfonyl Ketone

A novel and efficient method for the Cr­(II)-mediated desulfonylation of α-sulfonyl ketone by a Cr–ligand–Mn system has been developed during the course of process research on Halaven (eribulin mesylate). This reaction is dramatically accelerated in the presence of an appropriate bipyridyl-type ligand. This system is applicable to reduction of α-sulfur-substituted ketones. In addition, a Cr–Cp₂ZrCl₂–Mn catalytic system is also applicable to desulfonylation of α-sulfonyl ketone

Reconstitution of Biosynthetic Machinery for Indole-Diterpene Paxilline in <i>Aspergillus oryzae</i>

Indole-diterpenes represented by paxilline share a common pentacyclic core skeleton derived from indole and geranylgeranyl diphosphate. To shed light on the detailed biosynthetic mechanism of the paspaline-type hexacyclic skeleton, we examined the reconstitution of paxilline biosynthetic machinery in <i>Aspergillus oryzae</i> NSAR1. Stepwise introduction of the six <i>pax</i> genes enabled us to isolate all biosynthetic intermediates and to synthesize paxilline. In vitro and in vivo studies on the key enzymes, prenyltransferase PaxC and cyclase PaxB, allowed us to elucidate actual substrates of these enzymes. Using the isolated and the synthesized epoxide substrates, the highly intriguing stepwide epoxidation/cyclization mechanism for the construction of core structure has been confirmed. In addition, we also demonstrated “tandem transformation” to simultaneously introduce two genes using a single vector (<i>paxG</i>/<i>paxB</i>, pAdeA; <i>paxP</i>/<i>paxQ</i>, pUNA). This may provide further option for the reconstitution strategy to synthesize more complex fungal metabolites