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Hansen, L. M.

Publications and source records attributed to Hansen, L. M..

3 recordsLinked to original sources

Vaccination with Helicobacter pylori attachment proteins protects against gastric cancer

Most cases of gastric cancer are caused by chronic Helicobacter pylori infection, but the lack of early onco-diagnostics and a high risk for antibiotic resistance hampers early intervention through eradication of H. pylori infection by antibiotics. We reported on a protective mechanism where H. pylori gastric mucosal attachment can be reduced by natural antibodies that block the binding of its attachment protein BabA. Here we show that challenge infection with H. pylori induced response of such blocking antibodies in both human volunteers and in rhesus macaques, that mucosal vaccination with BabA protein antigen induced blocking antibodies in rhesus macaques, and that vaccination in a mouse model induced blocking antibodies that reduced gastric mucosal inflammation, preserved the gastric juice acidity, and fully protected the mice from gastric cancer caused by H. pylori.

immunology↗

Satellite Cell Expression of RAGE is Important for Collateral Vessel Formation

ObjectiveThe growth and remodeling of vascular networks is an important component of the prognosis for patients with peripheral artery disease. One protein that has been previously implicated to play a role in this process is the receptor for advanced glycation end products or RAGE. This study sought to determine the cellular source of RAGE in the ischemic hindlimb and the role of RAGE signaling in this cell type. Approach and ResultsUsing a hind limb ischemia model of vascular growth, this study found skeletal muscle satellite cells to be a novel major cellular source of RAGE in ischemic tissue by both staining and cellular sorting. While wild type satellite cells increased TNF and MCP-1 production in response to ischemia in vivo and a RAGE ligand in vitro, satellite cells from RAGE knockout mice lacked the increase in cytokine production both in vivo in response to ischemia and in vitro after stimuli with the RAGE ligand HMGB-1. Furthermore, encapsulated wild type satellite cells improved perfusion after hind limb ischemia surgery by both perfusion staining and vessel quantification but RAGE knockout satellite cells provided no improvement over empty capsules. ConclusionsThus, RAGE expression and signaling in satellite cells is crucial for their response to stimuli and angiogenic and arteriogenic functions. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=143 SRC="FIGDIR/small/433612v1_ufig1.gif" ALT="Figure 1"> View larger version (42K): org.highwire.dtl.DTLVardef@73dc28org.highwire.dtl.DTLVardef@7acb74org.highwire.dtl.DTLVardef@1c34bb1org.highwire.dtl.DTLVardef@9e62c8_HPS_FORMAT_FIGEXP M_FIG C_FIG

physiology↗

CagY-dependent regulation of type IV secretion in Helicobacter pylori is associated with alterations in integrin binding

Strains of Helicobacter pylori that cause ulcer or gastric cancer typically express a type IV secretion system (T4SS) encoded by the cag pathogenicity island (PAI). CagY is an ortholog of VirB10 that, unlike other VirB10 orthologs, has a large middle repeat region (MRR) with extensive repetitive sequence motifs, which undergo CD4+ T cell-dependent recombination during infection of mice. Recombination in the CagY MRR reduces T4SS function, diminishes the host inflammatory response, and enables the bacteria to colonize at a higher density. Since CagY is known to bind human 5{beta}1 integrin, we tested the hypothesis that recombination in the CagY MRR regulates T4SS function by modulating binding to 5{beta}1 integrin. Using a cell-free microfluidic assay, we found that H. pylori binding to 5{beta}1 integrin under shear flow is dependent on the CagY MRR, but independent of the presence of the T4SS pili, which are only formed when H. pylori is in contact with host cells. Similarly, expression of CagY in the absence of other T4SS genes was necessary and sufficient for whole bacterial cell binding to 5{beta}1 integrin. Bacteria with variant cagY alleles that reduced T4SS function showed comparable reduction in binding to 5{beta}1 integrin, though CagY was still expressed on the bacterial surface. We speculate that cagY-dependent modulation of H. pylori T4SS function is mediated by alterations in binding to 5{beta}1 integrin, which in turn regulates the host inflammatory response so as to maximize persistent infection.\n\nIMPORTANCEInfection with H. pylori can cause peptic ulcers, and is the most important risk factor for gastric cancer, the third most common cause of cancer death worldwide. The major H. pylori virulence factor that determines whether infection causes disease or asymptomatic colonization is the type IV secretion system (T4SS), a sort of molecular syringe that injects bacterial products into gastric epithelial cells and alters host cell physiology. We previously showed that recombination in CagY, an essential T4SS component, modulates the function of the T4SS. Here we found that these recombination events produce parallel changes in specific binding to 5{beta}1 integrin, a host cell receptor that is essential for T4SS-dependent translocation of bacterial effectors. We propose that CagY-dependent binding to 5{beta}1 integrin acts like a molecular rheostat that alters T4SS function and modulates the host immune response to promote persistent infection.

microbiology↗