Publications by authors named "V Valatas"

Background: Ulcerative colitis (UC) increases the risk for venous thromboembolism. Tissue factor (TF) initiates the extrinsic coagulation pathway (ECP).

Aims: To investigate the correlation of UC severity with latent ECP activation and TF expression in primary colonic stromal cells (PCSC).

View Article and Find Full Text PDF
Article Synopsis
  • Monocyte recruitment and inflammation in inflammatory bowel disease (IBD) are heavily influenced by the mucosal microenvironment, particularly through interactions involving stromal cells.
  • Researchers utilized single-cell sequencing and in vitro methods to explore how these stromal and myeloid cell interactions occur in Crohn's disease (CD) specifically in the ileum.
  • The study found that specific stromal cells produce chemokines like CCL2, which attract and promote the survival of inflammatory macrophages, suggesting potential new targets for IBD treatments focused on disrupting these inflammatory processes.
View Article and Find Full Text PDF

Background: Oncostatin-M (OSM) is associated with antitumor necrosis factor (anti-TNF)-α resistance in inflammatory bowel disease (IBD) and fibrosis in inflammatory diseases. We studied the expression of OSM and its receptors (OSMR, gp130) on intestinal subepithelial myofibroblasts (SEMFs) and the effect of OSM stimulation on SEMFs.

Methods: The mRNA and protein expression of OSM, OSMR, gp130, and several fibrotic and chemotactic factors were studied in mucosal biopsies and isolated human intestinal SEMFs of patients with IBD and healthy controls (HCs) and in a model of human intestinal organoids (HIOs).

View Article and Find Full Text PDF

Metabolites produced by dysbiotic intestinal microbiota can influence disease pathophysiology by participating in ligand-receptor interactions. Our aim was to investigate the differential expression of metabolite receptor (MR) genes between inflammatory bowel disease (IBD), healthy individuals (HIs), and disease controls in order to identify possible interactions with inflammatory and fibrotic pathways in the intestine. RNA-sequencing datasets containing 643 Crohn's disease (CD) patients, 467 ulcerative colitis (UC) patients and 295 HIs, and 4 -infected individuals were retrieved from the Sequence Read Archive, and differential expression was performed using the RaNA-seq online platform.

View Article and Find Full Text PDF

In steady state, intestinal subepithelial myofibroblasts form a thin layer below the basement membrane. Unlike the rest of the stromal cells in the lamina propria, they express tensile proteins, guide epithelial regeneration, and sense luminal microbiota. Upon inflammation in inflammatory bowel disease (IBD), they express activation markers, accept trophic signaling by infiltrating neutrophils and macrophages, and are activated by cytokines from helper T cells to produce a narrow spectrum of cytokines and a wider spectrum of chemokines, attract cells of innate and adaptive immunity, orchestrate inflammatory responses, and qualitatively and quantitatively modify the extracellular matrix.

View Article and Find Full Text PDF