Functional characterization of the complement receptor type 1 and its circulating ligands in patients with schizophrenia

<p>Abstract</p> <p>Background</p> <p>Whereas the complement system alterations contribute to schizophrenia, complement receptors and regulators are little studied. We investigated complement receptor type 1 (CR1) expression on blood cells, the levels of circulating immune complexes (CIC) containing ligands of CR1, C1q complement protein and fragments of C3 complement protein (C1q-CIC, C3d-CIC), and CR1 C5507G functional polymorphism in schizophrenia patients and controls.</p> <p>Results</p> <p>We found an increased C1q-CIC level and CR1 expression on blood cells, elevated number of CR1 positive erythrocytes and reduced number of CR1 positive lymphocytes and monocytes in patients compared to controls. No difference in the levels of C3d-CIC between groups was observed. Higher CR1 expression on erythrocytes in CC genotype versus CG+GG for both groups was detected, whereas no difference was observed for other cell populations. Our results indicated that schizophrenia is associated with the increased CR1 expression and C1q-CIC level.</p> <p>Conclusions</p> <p>Our study for the first time indicated that schizophrenia is associated with the increased CR1 expression and C1q-CIC level. Further studies in other ethnic groups are needed to replicate these findings.</p

Dynamic torsional resistance of nickel-titanium rotary instruments

Introduction: The cyclic fatigue of nickel-titanium (NiTi) rotary instruments has been studied extensively, but there is little information available on torsional fracture. Moreover, a clinical repeated locking effect was not considered in previous studies that evaluated torsional resistance of NiTi instruments. Thus, this study was aimed to compare the repetitive torsional resistance of various NiTi instruments with clinical relevance. Materials and Methods: Five brands of NiTi rotary instruments were selected: Twisted File (TF; SybronEndo, Orange, CA) and RaCe systems (FKG Dentaire, La Chaux-de-Fonds, Switzerland), both with an equilateral triangular cross-section, and the ProTaper (Dentsply Maillefer, Ballaignes, Switzerland), Helix (DiaDent, Chongju, Korea), and FlexMaster (VDW, Munchen, Germany), which had a convex triangular cross-section. Five millimeters of the tip of each file was embedded in composite resin block, and uniform torsional stresses (300 rpm, 1.0 N.cm) were applied repetitively by an endodontic motor with auto-stop mode until the file succumbed to torsional failure. The number of load applications leading to fracture was recorded. All fracture surfaces were examined under the SEM. Results were analyzed nonparametrically with α = 0.05. Results: Under the mode of load applications in this study, TF had the lowest and FlexMaster the highest torsional resistance among the groups (p < 0.05). Scanning electron microscopy examination revealed a typical pattern of torsional fracture for TF, RaCe, and ProTaper that was characterized by circular abrasion marks and skewed dimples near the center of rotation. In addition to these marks, Helix and FlexMaster presented a rough, torn-off appearance. Conclusion: It was concluded that files of same cross-sectional design may exhibit different resistance to fracture probably as a result of the manufacturing process. © 2010 American Association of Endodontists.link_to_subscribed_fulltex

Cell-Based Assays for Modeling Xenogeneic Immune Responses

Research in xenotransplantation implies a high experimental complexity comprising molecular, cellular, and in vivo studies to investigate the mechanisms of xenograft immune rejection and functional failure, as well as the strategies to counteract them. After major advances associated with the identification of the carbohydrate xenoantigens and their elimination through genomic edition of the source pigs, the study of the cellular immune response against the xenograft is gaining particular attention. Xenogeneic cell-based assays that put together pig cells and human leukocytes such as monocytes, NK cells, and T cells are relevant to address this hurdle. Thus, we describe here coculture, co-stimulatory, and cytotoxicity assays for investigating the cellular and molecular mechanisms of xenograft rejection. These techniques allow elucidating the key pathways that take place during the xenogeneic immune response in a simplified setting. Treatment with either pro-inflammatory or anti-inflammatory cytokines can be used for studying the regulation of adhesion, co-stimulatory molecules, and receptors involved in triggering the immune response under various conditions. Furthermore, these assays can be used for the follow-up of the immune response of in vivo studies as well as for the development of tolerogenic approaches that promote xenograft survival