108 research outputs found
Optimized protocol for the extraction of RNA and DNA from frozen whole blood sample stored in a single EDTA tube
Cryopreservation of whole blood is useful for DNA collection, and clinical and basic research. Blood samples in ethylenediaminetetraacetic acid disodium salt (EDTA) tubes stored at − 80 °C are suitable for DNA extraction, but not for high-quality RNA extraction. Herein, a new methodology for high-quality RNA extraction from human blood samples is described. Quickly thawing frozen whole blood on aluminum blocks at room temperature could minimize RNA degradation, and improve RNA yield and quality compared with thawing the samples in a 37 °C water bath. Furthermore, the use of the NucleoSpin RNA kit increased RNA yield by fivefold compared with the PAXgene Blood RNA Kit. Thawing blood samples on aluminum blocks significantly increased the DNA yield by ~ 20% compared with thawing in a 37 °C water bath or on ice. Moreover, by thawing on aluminum blocks and using the NucleoSpin RNA and QIAamp DNA Blood kits, the extraction of RNA and DNA of sufficient quality and quantity was achieved from frozen EDTA whole blood samples that were stored for up to 8.5 years. Thus, extracting RNA from frozen whole blood in EDTA tubes after long-term storage is feasible. These findings may help advance gene expression analysis, as well as biomarker research for various diseases
Interferon signaling and hypercytokinemia-related gene expression in the blood of antidepressant non-responders
Only 50% of patients with depression respond to the first antidepressant drug administered. Thus, biomarkers for prediction of antidepressant responses are needed, as predicting which patients will not respond to antidepressants can optimize selection of alternative therapies. We aimed to identify biomarkers that could predict antidepressant responsiveness using a novel data-driven approach based on statistical pattern recognition. We retrospectively divided patients with major depressive disorder into antidepressant responder and non-responder groups. Comprehensive gene expression analysis was performed using peripheral blood without narrowing the genes. We designed a classifier according to our own discrete Bayes decision rule that can handle categorical data. Nineteen genes showed differential expression in the antidepressant non-responder group (n = 15) compared to the antidepressant responder group (n = 15). In the training sample of 30 individuals, eight candidate genes had significantly altered expression according to quantitative real-time polymerase chain reaction. The expression of these genes was examined in an independent test sample of antidepressant responders (n = 22) and non-responders (n = 12). Using the discrete Bayes classifier with the HERC5, IFI6, and IFI44 genes identified in the training set yielded 85% discrimination accuracy for antidepressant responsiveness in the 34 test samples. Pathway analysis of the RNA sequencing data for antidepressant responsiveness identified that hypercytokinemia- and interferon-related genes were increased in non-responders. Disease and biofunction analysis identified changes in genes related to inflammatory and infectious diseases, including coronavirus disease. These results strongly suggest an association between antidepressant responsiveness and inflammation, which may be useful for future treatment strategies for depression
Soft X-Ray CT Imaging of a Low-Aspect-Ratio Toroidal Plasma Maintained Solely by Electron Cyclotron Heating
Images of soft X-ray (SX) emission in a poloidal cross section have been reconstructed by computer tomography from 80 chord-integrated signals in total obtained in a low-aspect-ratio toroidal plasma produced and maintained solely by electron cyclotron (EC) heating on the LATE device. The SX images show the heating characteristics by electron Bernstein waves under the existence of multiharmonics of EC resonance in the low-aspect-ratio toroidal plasma
Probiotic (yogurt) containing Lactobacillus gasseri OLL2716 is effective for preventing Candida albicans-induced mucosal inflammation and proliferation in the forestomach of diabetic rats
Oral and esophageal candidiasis sometimes
leads to mucosal hyperplasia, and progresses to
carcinoma. We have produced an animal model for
hyperplastic mucosal candidiasis in the forestomach that
has a proliferative lesion of the squamous epithelium
with chronic inflammation and C. albicans infection,
some of which advanced to squamous cell carcinoma.
There are many reports of the antibacterial effects of
probiotics, but consensus about their antifungal effect
has not been reached. In the present study, we
investigate whether probiotic (yogurt) containing
Lactobacillus gasseri OLL2716 (LG21 yogurt) can
prevent proliferative and inflammatory changes caused
by C. albicans in this mucosal candidiasis animal model.
Diabetes was induced in 8-week-old WBN/Kob rats by
intravenous administration of alloxan. One group of
diabetic rats received a saline containing C. albicans and
LG21 yogurt orally (DC+LG21 group) for 30 weeks,
and another group received only C. albicans (DC group)
for 30 weeks. They were sacrificed at 40 weeks of age,
and analyzed histopathologically. In the DC+LG21
group, squamous hyperplasia at the greater curvature
was significantly milder, and the Ki-67 positive index
was significantly lower compared with the DC group.
Suppurative inflammation with C. albicans also tended
to be suppressed at the greater curvature. These findings
suggest that probiotic (yogurt) containing Lactobacillus
gasseri OLL2716 can suppress squamous hyperplastic
change and inflammation associated with C. albicans
infection in the forestomach
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