Extracellular Matrix of Collagen Modulates Arrhythmogenic Activity of Pulmonary Veins through p38 MAPK Activation Scientists evaluated whether collagen can directly modulate pulmonary vein (PV) arrhythmogenesis. Action potentials and ionic currents were investigated in isolated male New Zealand rabbit PV cardiomyocytes with and without collagen incubation using the whole-cell patch-clamp technique. [J Mol Cell Cardiol] Abstract Discoidin Domain Receptor 1 Is a Novel Modulator of Megakaryocyte-Collagen Interactions The authors demonstrated the expression of the novel collagen receptor Discoidin Domain Receptor 1 (DDR1) by human megakaryocytes (MKs) at both mRNA and protein levels and provide evidence of DDR1 involvement in the regulation of MK motility on type I collagen through a mechanism based on the activity of SHP1 phosphatase and Syk tyrosine kinase. [J Biol Chem] Abstract | Full Article Comparative Proteomic Analysis of Normal and Collagen IX Null Mouse Cartilage Reveals Altered Extracellular Matrix Composition and Novel Components of the Collagen IX Interactome To investigate the molecular basis of the collagen IX null phenotype, researchers analyzed differences in protein abundance between wild-type and knockout cartilage by capHPLC tandem mass spectrometry. Components that were differentially abundant between wild-type and collagen IX deficient cartilage included 15 extracellular matrix proteins. [J Biol Chem] Abstract | Full Article Inflammatory Environment Induces Gingival Tissue-Specific Mesenchymal Stem Cells to Differentiate towards a Pro-Fibrotic Phenotype Under the influence of the inflammatory cytokines, gingival tissue-specific mesenchymal stem cells exhibited higher rate of proliferation than those under normal condition, while their potential for osteogenic and adipogenic differentiation was suppressed. The expression of matrix metalloproteinases (MMP)-1, MMP-2, IL-1, IL-6, TNF-α and type 1 collagen was significantly higher in inflammatory gingival tissues than in normal gingival tissues. [Biol Cell] Abstract Type VIII Collagen Signals via β1 Integrin and RhoA to Regulate MMP-2 Expression and Smooth Muscle Cell Migration Smooth muscle cells isolated from wild-type C57BL/6 and type VIII collagen deficient mice were studied using assays to measure chemotactic and haptotactic migration, and remodeling and contraction of 3-dimensional type I collagen gels. [Matrix Biol] Abstract Type IV Collagen Stimulates Pancreatic Cancer Cell Proliferation, Migration, and Inhibits Apoptosis through an Autocrine Loop The expression of type IV collagen and its integrin receptors were examined in vivo in human pancreatic cancer tissue. The cellular effects of type IV collagen were studied in pancreatic cancer cell lines by reducing type IV collagen expression through RNA interference and by functional receptor blocking of integrins and their binding-sites on the type IV collagen molecule. [BMC Cancer] Abstract | Full Article Poly(L-lactide-co-glycolide) Scaffolds Coated with Collagen and Glycosaminoglycans: Impact on Proliferation and Osteogenic Differentiation of Human Mesenchymal Stem Cells Scientists analyzed poly(L-lactide-co-glycolide) scaffolds modified with artificial extracellular matrices (aECM) consisting of collagen type I, chondroitin sulphate, and sulphated hyaluronan. They investigated the effect of these aECM coatings on proliferation and osteogenic differentiation of human mesenchymal stem cells in vitro. [J Biomed Mater Res Part A] Abstract Epigallocatechin-3-Gallate Inhibits Collagen Production of Nasal Polyp-Derived Fibroblasts The authors aimed to determine the effect of (-)-epigallocatechin-3-gallate (EGCG) on fibroblast differentiation into myofibroblasts and extracellular matrix accumulation in transforming growth factor (TGF)-β1-induced nasal polyp-derived fibroblasts (NPDFs), and to determine if the antioxidative effect of EGCG on reactive oxygen species production in TGF-β1-induced NPDFs is involved in the aforementioned processes. [Phytother Res] Abstract Glycosaminoglycan Mimetic Associated to Human Mesenchymal Stem Cell Based Scaffolds Inhibit Ectopic Bone Formation but Induce Angiogenesis In Vivo Researchers developed a strategy associating the glycosaminoglycans mimetic [OTR4120] with bone substitutes to optimize stem cell-based therapeutic products. They showed that [OTR4120] was able to potentiate proliferation, migration and osteogenic differentiation of human mesenchymal stem cells in vitro. [Tissue Eng Part A] Abstract |