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Aim: To study the effect of Rapamycin (RAPA) and Cyclosporin A (CsA) on the expression of TLR5 and Foxp3 in allotransplantation model in vivo.
Methods: The murine model of skin allotransplantation was established, and divided into three groups, injected with CsA 10 mg/(kg.d), RAPA 1.5 mg/(kg.d)) and normal saline respectively for 14 consecutive days. The grafts survival was observed daily. The expression of TLR5 and Foxp3 mRNA was detected by RT-PCR.
Results: The survival time was obviously longer in RAPA and CsA treated groups than control group. The expression of TLR5 mRNA in allotransplantation treated with RAPA was higher than that in control group(P<0.05) and remained at a higher level than the other two groups until day 21. TLR5 showed the highest expression on day 10 among three groups, which was the top point of allorejection. Compared with CsA group, RAPA treatment in vivo caused the higher expression of Foxp3 mRNA(P<0.05), which remained at a high level after treatment stopped. However, in CsA group, Foxp3 mRNA expression increased on day 7 and 10, and then decreased significantly on day 14. TLR5 and Foxp3 expression was positively correlated among three groups. RAPA and CsA promoted the expression of TLR5 in T cells when treated with flagellin for 6 hours in vitro and RAPA has stronger effect.
Conclusion: RAPA and CsA can promote the expression of TLR5 and Foxp3 in allotransplantation model in vivo and flagellin enhanced this effect in vitro.
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BMJ Open Diabetes Res Care
September 2025
Veterinary and Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Frederiksberg Campus, Frederiksberg, Denmark.
Unlabelled: In mammalian and human life, it is important that the immune system defends against microorganisms. Although there is a huge overlap, innate cells are good against bacteria, whereas T cells are good against viruses, mainly because of antibody production via T helper and B lymphocytes. Toll-like receptor 5 (TLR5) is a regulator; when it is highly expressed, T cells are inhibited, and innate cells are favored.
View Article and Find Full Text PDFPNAS Nexus
September 2025
Institute of Molecular Biology, Academia Sinica, Taipei 11529, Taiwan.
endoribonuclease E (RNase E), encoded by the essential gene and conserved across γ-Proteobacteria, plays a central role in RNA processing and decay. We show here that -null strain, -null strain complemented with catalytic-null RNase E mutant, and C-terminal-truncated strain (Rned500) all lack flagellar biogenesis and motility under both aerobic and anaerobic conditions, which are restored by wild-type RNase E complementation. The Rned500 displays dysregulated expression of the three-tiered flagellar transcriptional cascade, increased stability of flagellar mRNAs, and reduced flagellar protein levels through sRNA-dependent translational inhibition.
View Article and Find Full Text PDFPoult Sci
August 2025
Division of Avian Infectious Diseases, State Key Laboratory for Animal Disease Control and Prevention, Harbin Veterinary Research Institute, the Chinese Academy of Agricultural Sciences, Harbin 150001, China. Electronic address:
In addition to its nutritional role in regulating calcium and phosphorus metabolism, vitamin D also possesses immunoregulatory effects. Herein, we used chicken embryo fibroblast cells (CEFs) to study the effect of 1,25-dihydroxyvitamin D (1,25(OH)D) on the immune response induced by infectious bronchitis virus (IBV) infection. We observed the inhibition to virus proliferation in the cells by adding 10 nM 1,25(OH)D.
View Article and Find Full Text PDFPharmaceuticals (Basel)
August 2025
Plataforma Zebrafish of the Laboratory of Applied Toxinology (CeTICS/FAPESP), Butantan Institute, São Paulo 05503-900, Brazil.
The candidate therapeutic peptide TnP demonstrates broad, system-level regulatory capacity, revealed through integrated network analysis from transcriptomic data in zebrafish. Our study primarily identifies TnP as a multifaceted modulator of drug metabolism, wound healing, proteolytic activity, and pigmentation pathways. Transcriptomic profiling of TnP-treated larvae following tail fin amputation revealed 558 differentially expressed genes (DEGs), categorized into four functional networks: (1) drug-metabolizing enzymes (, ) and transporters (SLC/ABC families), where TnP alters xenobiotic processing through Phase I/II modulation; (2) cellular trafficking and immune regulation, with upregulated myosin genes (/) enhancing wound repair and - signaling fine-tuning inflammation; (3) proteolytic cascades (, ) coupled to autophagy (, ) and metabolic rewiring (- axis); and (4) melanogenesis-circadian networks (/-) linked to ubiquitin-mediated protein turnover.
View Article and Find Full Text PDFPLoS Pathog
August 2025
Department of Medicine, Divisions of Cardiovascular Medicine, UMass Chan Medical School, Worcester, Massachusetts, United States of America.
Respiratory infections are characterized by an increased risk of thrombosis, likely involving platelet-leukocyte crosstalk via pattern recognition receptors (PRRs). Here we characterized COVID19-mediated changes in PRR levels and their associations with thrombotic/coagulation-related transcriptional programs across platelets and leukocytes and assessed their correlation with COVID19 outcomes. Amplicon RNAseq of platelets and leukocytes from COVID19 patients (n = 10) and non-infected donors (n = 15) showed distinct patterns of PRR-expression levels based on cell type.
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