Bertaux-Skeirik Nina, Feng Rui, Schumacher Michael A, Li Jing, Mahe Maxime M, Engevik Amy C, Javier Jose E, Peek Richard M, Ottemann Karen, Orian-Rousseau Veronique, Boivin Gregory P, Helmrath Michael A, Zavros Yana
Department of Molecular and Cellular Physiology, University of Cincinnati, Cincinnati, Ohio, United States of America.
Department of Surgery, Division of Pediatric Surgery, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States of America.
PLoS Pathog. 2015 Feb 6;11(2):e1004663. doi: 10.1371/journal.ppat.1004663. eCollection 2015 Feb.
The cytotoxin-associated gene (Cag) pathogenicity island is a strain-specific constituent of Helicobacter pylori (H. pylori) that augments cancer risk. CagA translocates into the cytoplasm where it stimulates cell signaling through the interaction with tyrosine kinase c-Met receptor, leading cellular proliferation. Identified as a potential gastric stem cell marker, cluster-of-differentiation (CD) CD44 also acts as a co-receptor for c-Met, but whether it plays a functional role in H. pylori-induced epithelial proliferation is unknown. We tested the hypothesis that CD44 plays a functional role in H. pylori-induced epithelial cell proliferation. To assay changes in gastric epithelial cell proliferation in relation to the direct interaction with H. pylori, human- and mouse-derived gastric organoids were infected with the G27 H. pylori strain or a mutant G27 strain bearing cagA deletion (∆CagA::cat). Epithelial proliferation was quantified by EdU immunostaining. Phosphorylation of c-Met was analyzed by immunoprecipitation followed by Western blot analysis for expression of CD44 and CagA. H. pylori infection of both mouse- and human-derived gastric organoids induced epithelial proliferation that correlated with c-Met phosphorylation. CagA and CD44 co-immunoprecipitated with phosphorylated c-Met. The formation of this complex did not occur in organoids infected with ∆CagA::cat. Epithelial proliferation in response to H. pylori infection was lost in infected organoids derived from CD44-deficient mouse stomachs. Human-derived fundic gastric organoids exhibited an induction in proliferation when infected with H. pylori that was not seen in organoids pre-treated with a peptide inhibitor specific to CD44. In the well-established Mongolian gerbil model of gastric cancer, animals treated with CD44 peptide inhibitor Pep1, resulted in the inhibition of H. pylori-induced proliferation and associated atrophic gastritis. The current study reports a unique approach to study H. pylori interaction with the human gastric epithelium. Here, we show that CD44 plays a functional role in H. pylori-induced epithelial cell proliferation.
细胞毒素相关基因(Cag)致病岛是幽门螺杆菌(H. pylori)的一种菌株特异性成分,可增加患癌风险。CagA易位至细胞质,通过与酪氨酸激酶c-Met受体相互作用刺激细胞信号传导,导致细胞增殖。分化簇(CD)CD44被鉴定为一种潜在的胃干细胞标志物,它也是c-Met的共受体,但它是否在幽门螺杆菌诱导的上皮细胞增殖中发挥功能作用尚不清楚。我们检验了CD44在幽门螺杆菌诱导的上皮细胞增殖中发挥功能作用这一假设。为了测定与幽门螺杆菌直接相互作用相关的胃上皮细胞增殖变化,将人源和小鼠源胃类器官用G27幽门螺杆菌菌株或携带cagA缺失的突变G27菌株(∆CagA::cat)感染。通过EdU免疫染色对上皮细胞增殖进行定量。通过免疫沉淀分析c-Met的磷酸化,随后进行蛋白质印迹分析以检测CD44和CagA的表达。人源和小鼠源胃类器官的幽门螺杆菌感染均诱导了与c-Met磷酸化相关的上皮细胞增殖。CagA和CD44与磷酸化的c-Met共免疫沉淀。在感染∆CagA::cat的类器官中未形成这种复合物。源自CD44缺陷小鼠胃的感染类器官中,对幽门螺杆菌感染的上皮细胞增殖反应丧失。人源胃底胃类器官在感染幽门螺杆菌时表现出增殖诱导,而在用CD44特异性肽抑制剂预处理的类器官中未观察到这种情况。在成熟的蒙古沙鼠胃癌模型中,用CD44肽抑制剂Pep1处理的动物,导致幽门螺杆菌诱导的增殖和相关萎缩性胃炎受到抑制。本研究报告了一种研究幽门螺杆菌与人胃上皮细胞相互作用的独特方法。在此,我们表明CD44在幽门螺杆菌诱导的上皮细胞增殖中发挥功能作用。