Antimicrobial peptide LL-37 promotes bacterial phagocytosis by human macrophages.
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Antimicrobial peptides in 2014On the Functional Overlap between Complement and Anti-Microbial PeptidesRegulation of calcitriol biosynthesis and activity: focus on gestational vitamin D deficiency and adverse pregnancy outcomes.High temperature affects the phagocytic activity of human peripheral blood mononuclear cells.Significant Effects of Oral Phenylbutyrate and Vitamin D3 Adjunctive Therapy in Pulmonary Tuberculosis: A Randomized Controlled Trial.The microbiome at the pulmonary alveolar niche and its role in Mycobacterium tuberculosis infectionButyrate upregulates endogenous host defense peptides to enhance disease resistance in piglets via histone deacetylase inhibition.Identification of Human Cathelicidin Peptide LL-37 as a Ligand for Macrophage Integrin αMβ2 (Mac-1, CD11b/CD18) that Promotes Phagocytosis by Opsonizing Bacteria.Topical cathelicidin (LL-37) an innate immune peptide induces acute olfactory epithelium inflammation in a mouse model.B Cell Functions Can Be Modulated by Antimicrobial Peptides in Rainbow Trout Oncorhynchus mykiss: Novel Insights into the Innate Nature of B Cells in Fish.P. gingivalis in Periodontal Disease and Atherosclerosis - Scenes of Action for Antimicrobial Peptides and Complement.Immuno-Stimulatory Peptides as a Potential Adjunct Therapy against Intra-Macrophagic Pathogens.Quantifying Phagocytosis by Immunofluorescence and Microscopy.Phenylbutyrate induces LL-37-dependent autophagy and intracellular killing of Mycobacterium tuberculosis in human macrophagesP2X7 Receptor Regulates Internalization of Antimicrobial Peptide LL-37 by Human Macrophages That Promotes Intracellular Pathogen Clearance.An Essential Role for TAGLN2 in Phagocytosis of Lipopolysaccharide-activated Macrophages.Mouse Bone Marrow Sca-1+ CD44+ Mesenchymal Stem Cells Kill Avirulent Mycobacteria but Not Mycobacterium tuberculosis through Modulation of Cathelicidin Expression via the p38 Mitogen-Activated Protein Kinase-Dependent Pathway.Cathelicidin-deficient mice exhibit increased survival and upregulation of key inflammatory response genes following cecal ligation and puncture.Signals of vagal circuits engaging with AKT1 in α7 nAChR+CD11b+ cells lessen E. coli and LPS-induced acute inflammatory injury.Interspecies cathelicidin comparison reveals divergence in antimicrobial activity, TLR modulation, chemokine induction and regulation of phagocytosis.Editorial: Antimicrobial Peptides and Complement - Maximising the Inflammatory Response.Amphiphilic tobramycins with immunomodulatory properties.CRAMP deficiency leads to a pro-inflammatory phenotype and impaired phagocytosis after exposure to bacterial meningitis pathogens.LL-37 peptide enhancement of signal transduction by Toll-like receptor 3 is regulated by pH: identification of a peptide antagonist of LL-37.Control of Phagocytosis by Microbial Pathogens.P17, an Original Host Defense Peptide from Ant Venom, Promotes Antifungal Activities of Macrophages through the Induction of C-Type Lectin Receptors Dependent on LTB4-Mediated PPARγ Activation.Mudskipper (Boleophthalmus pectinirostris) Hepcidin-1 and Hepcidin-2 Present Different Gene Expression Profile and Antibacterial Activity and Possess Distinct Protective Effect against Edwardsiella tarda Infection.The influence of rosuvastatin on the gastrointestinal microbiota and host gene expression profiles.Combating Multidrug-Resistant Pathogens with Host-Directed Nonantibiotic Therapeutics.Impact of high-dose vitamin D3 on plasma free 25-hydroxyvitamin D concentrations and antimicrobial peptides in critically ill mechanically ventilated adults.Comparing naturally occurring glycosylated forms of proline rich antibacterial peptide, Drosocin.Partners in crime: neutrophils and monocytes/macrophages in inflammation and disease.For when bacterial infections persist: Toll-like receptor-inducible direct antimicrobial pathways in macrophages.TAGLN2 polymerizes G-actin in a low ionic state but blocks Arp2/3-nucleated actin branching in physiological conditions.Phenotypic, functional, and plasticity features of classical and alternatively activated human macrophages.Cathelicidins: Immunomodulatory Antimicrobials
P2860
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P2860
Antimicrobial peptide LL-37 promotes bacterial phagocytosis by human macrophages.
description
2014 nî lūn-bûn
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name
Antimicrobial peptide LL-37 promotes bacterial phagocytosis by human macrophages.
@en
Antimicrobial peptide LL-37 promotes bacterial phagocytosis by human macrophages.
@nl
type
label
Antimicrobial peptide LL-37 promotes bacterial phagocytosis by human macrophages.
@en
Antimicrobial peptide LL-37 promotes bacterial phagocytosis by human macrophages.
@nl
prefLabel
Antimicrobial peptide LL-37 promotes bacterial phagocytosis by human macrophages.
@en
Antimicrobial peptide LL-37 promotes bacterial phagocytosis by human macrophages.
@nl
P2093
P356
P1476
Antimicrobial peptide LL-37 promotes bacterial phagocytosis by human macrophages.
@en
P2093
Anne M van der Does
Birgitta Agerberth
Jesper Z Haeggström
Lennart Lindbom
P304
P356
10.1189/JLB.0513304
P577
2014-02-18T00:00:00Z