Searching for MgII absorbers in and around galaxy clusters

To study environmental effects on the circumgalactic medium (CGM), we use the samples of redMaPPer galaxy clusters, background quasars and cluster galaxies from the SDSS. With ~82 000 quasar spectra, we detect 197 MgII absorbers in and around the clusters. The detection rate per quasar is 2.7$\pm$0.7 times higher inside the clusters than outside the clusters, indicating that MgII absorbers are relatively abundant in clusters. However, when considering the galaxy number density, the absorber-to-galaxy ratio is rather low inside the clusters. If we assume that MgII absorbers are mainly contributed by the CGM of massive star-forming galaxies, a typical halo size of cluster galaxies is smaller than that of field galaxies by 30$\pm$10 per cent. This finding supports that galaxy haloes can be truncated by interaction with the host cluster.Comment: 11 pages, 12 figures. To appear in MNRA

Newly designed coil tube for bowel decompression in patients with small bowel obstructions

AbstractBackgroundThe purpose of this study was to clinically evaluate a coil tube that we recently designed for bowel decompression in patients with a small bowel obstruction.MethodsThe coil tube was composed of a stainless steel coil, a polyolefin tube, and a rubber adaptor. The tube was inserted under fluoroscopic guidance in 14 consecutive patients with small bowel obstructions. Technical success was defined as insertion of the distal end of the tube into at least the proximal jejunum, and clinical success was defined as intestinal decompression and relief of obstructive symptoms.ResultsThe technical success rate was 100%. Clinical success was achieved in 12 patients (86%). The clinical failures were a patient with peritoneal carcinomatosis and an ileocolic fistula, and a patient with bezoars following intestinal hemorrhage. No coil-related complications occurred.ConclusionOur newly designed coil tube was safe and effective in patients with bowel decompression associated with a small bowel obstruction. In addition, our tube has several advantages over other currently used tube types

Expression of Osteocalcin and Transglutaminase and Labelling of Bromodeoxyuridine during Fracture Healing in the Rat Tibia

The expression of osteocalcin and transglutaminase C(TGase C) during fracture healing was inwstigated with immunohistochemical studies. A transverse osteotomy was made at the proximal tibia in Sprague-Dawley male rats and immobilized with a small external skeletal fixator. The animals lU!l'e sacrificed serially I, 3, 5, 7, 14, 42 days respectively after fracture. Longitudinal sections of the healing bone were stained with pohclonal antibody against osteocalcin and TGase C, and monoclonal antibody against bromodeoxyuridine. During the intramembranous bone formation at the periosteum around the fracture site, osteocalcin was strongly expressed in the proliferating osteoprogenitor cells from the 1st day of fracture, and then, in osteoblasts, osteoid matrix and osteocytes. The expression of TGase C was weakly positive in both osteoprogenitor cells and osteoblasts. Ai the site of endochondral bone formation, which was first reoealed 5 days after fracture, cell proliferation occurred at the periphery of cartilaginous callus where the number of cells stained with BrdU was highest During the maturation of callus, those cells uere entrapped in the chondroid matrix and became larger and larger. Osteocalcin was demonstrated in the cytoplasm of chondrocytes, while chondroid matrix was negatiwly stained. TGase C was found in the cytoplasm of more centrally located and matured chondrocytes as compared with osteocalcin. Osteoid matrix was stained with osteocalcin but not with TGase C. These finding may suggest that osteocalcin participates in the early phase of endochondral bone formation, while TGase C participates in the late phase, suggesting the role of TGase C in matrix stabilization. But the reason for the difference in the expression of TGase C between the endochondral bone formation and intramembranous bone formation should be further inwstigated. Healing of IAA2Il immobilized fracture in this study was predominantly induced by intramembranous ossification rather than endochondral ossification. Periosteal osteoprogenitor cells appeared to initiate and to lead bone formation after osteotomy. These findings indicate that preservation of the periosteum is essential to achieve successful fracture healing

Purification of Sulfhydryl Oxidase from Human Foreskin Tissue and Immunohistochemical Localization

Human sulfhydryl oxidase, catalyzing the conversion of either free or bound thiol to disulfide compound, was isolated from human skin tissue to apparent homogeneity through multiple steps of ammonium sulfate salting-out, DEAE-cellulose chromatography, CM-cellulose chromatography and ACA54 gel filtration. The enzyme was shown to have a molecular weight of 65 kDa and a specific activity of 8.39 x 103 Ufmg protein. The specific polyclonal antibody was raised, with which the tissue distribution of the enzyme was studied immunohistochemically. The enzyme is present ubiquitously in most human tissues. However, the granular layer of the epidermis, stromal tissues of the breast and uterine cervix, hepatocytes and islets of the pancreas are noted to contain a comparatively high amount of the enzyme

Fiber Type Specific Presence of GIutathione Transferase Isoenzymes in the Rat SkeIetaI Musele Tissue

Glutathione transferases (GST) are a group of enzymes, majorly responsible for biochemical detoxification by conjugating glutathione to a set of hydrophobic ligands. The tissue isoenzyme pattern of the enzymes has been well illustrated with their significance of histological localization. But in the cases of muscle tissue, the GST isoenzyme pattern has not yet been clearly studied. In the present experiment, we have carried out an immunohistochemical analysis on the distribution of GST isoenzymes using anti GST-P and anti GST-L antibodies on cardiac, smooth and skeletal muscle tissues. The results showed that the intestinal smooth muscle and cardiac muscles are very weakly immunostained for both anti GST-L and P antibodies. In contrast, major bundles of skeletal muscles were positively responsive to GST-L antibody. Therefore, we compared the expression of GST-L in the muscle tissues of the soleus and plantaris, which were composed dominantly of type I fiber and type II fiber, respectively. The data indicated that only type II fibers in the plantaris muscle tissue were positive to GST-L antibody, which was confirmed by specific ATPase staining. And the soleus muscle, consisting mainly of type I fibers, contains a higher amount of GST-P isoenzyme than the plantaris muscle. Therefore, it can be suggested that the expression of GST isoenzyme can be used as a type-specific marker for the type II fiber of skeletal muscles. And moreover, the differential pattern of GST isoenzymes in those muscle tissues according to fiber types may contribute to explaining the differences in fatigue-sensitivity of muscles to exercise

Determining the influence of ship hull deformations caused by draught change on shaft alignment application using FE analysis

This paper was to address the shortcomings of current design practice to evaluate the stability of the shaft alignment for a 300,000 DWT Very Large Crude Oil Carrier. An enhanced approach using FE was applied to identify the influence of hull deformation on the alignment of the shafting system. The effectiveness of this method was demonstrated in comparison with Jack up technique. Analysis results showed that the hull deformation could be a key factor affecting the offset distortion of each bearing supporting the shaft line. Moreover, it was confirmed that the deformation pattern of cargo hold was opposite to the deformation of engine room structure when hull deformation occurred due to draught change of the case ship. As new research findings, they are believed to contribute significantly to the prevention of shaft damage associated with hull deformations, thereby improving the reliability of shaft alignment for similar types of vessels

Homeobox gene Dlx-2 is implicated in metabolic stress-induced necrosis

<p>Abstract</p> <p>Background</p> <p>In contrast to tumor-suppressive apoptosis and autophagic cell death, necrosis promotes tumor progression by releasing the pro-inflammatory and tumor-promoting cytokine high mobility group box 1 (HMGB1), and its presence in tumor patients is associated with poor prognosis. Thus, necrosis has important clinical implications in tumor development; however, its molecular mechanism remains poorly understood.</p> <p>Results</p> <p>In the present study, we show that Distal-less 2 (Dlx-2), a homeobox gene of the Dlx family that is involved in embryonic development, is induced in cancer cell lines dependently of reactive oxygen species (ROS) in response to glucose deprivation (GD), one of the metabolic stresses occurring in solid tumors. Increased Dlx-2 expression was also detected in the inner regions, which experience metabolic stress, of human tumors and of a multicellular tumor spheroid, an <it>in vitro </it>model of solid tumors. Dlx-2 short hairpin RNA (shRNA) inhibited metabolic stress-induced increase in propidium iodide-positive cell population and HMGB1 and lactate dehydrogenase (LDH) release, indicating the important role(s) of Dlx-2 in metabolic stress-induced necrosis. Dlx-2 shRNA appeared to exert its anti-necrotic effects by preventing metabolic stress-induced increases in mitochondrial ROS, which are responsible for triggering necrosis.</p> <p>Conclusions</p> <p>These results suggest that Dlx-2 may be involved in tumor progression via the regulation of metabolic stress-induced necrosis.</p

Microvasculature remodeling in the mouse lower gut during inflammaging

Inflammaging is defined as low-grade, chronic, systemic inflammation in aging, in the absence of overt infection. Age-associated deterioration of gastrointestinal function could be ascribed to the inflammaging, although evidence is yet to emerge. Here we show that microvessels in aging mouse intestine were progressively deprived of supportive structures, microvessel-associated pericytes and adherens junction protein vascular endothelial (VE)-cadherin, and became leaky. This alteration was ascribed to up-regulation of angiopoetin-2 in microvascular endothelial cells. Up-regulation of the angiopoietin-2 was by TNF-α, originated from M2-like residential CD206 + macrophages, proportion of which increases as animal ages. It was concluded that antigenic burdens encountered in intestine throughout life create the condition of chronic stage of inflammation, which accumulates M2-like macrophages expressing TNF-α. The TNF-α induces vascular leakage to facilitate recruitment of immune cells into intestine under the chronic inflammatory setting. © Author(s) 2017.1