Details

Autor(en) / Beteiligte

• Nagy, Toni A
• Wroblewski, Lydia E
• Wang, Dingzhi
• Piazuelo, M. Blanca
• Delgado, Alberto
• Romero–Gallo, Judith
• Noto, Jennifer
• Israel, Dawn A
• Ogden, Seth R
• Correa, Pelayo
• Cover, Timothy L
• Peek, Richard M

Titel

β-Catenin and p120 Mediate PPARδ-Dependent Proliferation Induced by Helicobacter pylori in Human and Rodent Epithelia

Ist Teil von

• Gastroenterology (New York, N.Y. 1943), 2011-08, Vol.141 (2), p.553-564

Ort / Verlag

United States: Elsevier Inc

Erscheinungsjahr

2011

Quelle

Elsevier ScienceDirect Journals

Beschreibungen/Notizen

• Background & Aims Colonization of gastric mucosa by Helicobacter pylori leads to epithelial hyperproliferation, which increases the risk for gastric adenocarcinoma. One H pylori virulence locus associated with cancer risk, cag , encodes a secretion system that transports effectors into host cells and leads to aberrant activation of β-catenin and p120-catenin (p120). Peroxisome proliferator-activated receptor (PPAR)δ is a ligand-activated transcription factor that affects oncogenesis in conjunction with β-catenin. We used a carcinogenic H pylori strain to define the role of microbial virulence constituents and PPARδ in regulating epithelial responses that mediate development of adenocarcinoma. Methods Gastric epithelial cells or colonies were co-cultured with the H pylori cag + strain 7.13 or cagE− , cagA − , soluble lytic transglycosylase − , or cagA − /soluble lytic transglycosylase − mutants. Levels of PPARδ and cyclin E1 were determined by real-time, reverse-transcription polymerase chain reaction, immunoblot analysis, or immunofluorescence microscopy; proliferation was measured in 3-dimensional culture. PPARδ and Ki67 expression were determined by immunohistochemical analysis of human biopsies and rodent gastric mucosa. Results H pylori induced β-catenin– and p120-dependent expression and activation of PPARδ in gastric epithelial cells, which were mediated by the cag secretion system substrates CagA and peptidoglycan. H pylori stimulated proliferation in vitro, which required PPARδ-mediated activation of cyclin E1; H pylori did not induce expression of cyclin E1 in a genetic model of PPARδ deficiency. PPARδ expression and proliferation in rodent and human gastric tissue was selectively induced by cag + strains and PPARδ levels normalized after eradication of H pylori. Conclusions The H pylori cag secretion system activates β-catenin, p120, and PPARδ, which promote gastric epithelial cell proliferation via activation of cyclin E1. PPARδ might contribute to gastric adenocarcinoma development in humans.