PGE(2) /EP(4) receptor attenuated mucosal injury via β-arrestin1/Src/EGFR-mediated proliferation in portal hypertensive gastropathy.

BACKGROUND AND PURPOSE: Portal hypertensive gastropathy (PHG) is a serious complication of liver cirrhosis and a potential cause of bleeding in patients with cirrhosis. Suppressed mucosal epithelial proliferation is a crucial pathological characteristic of PHG. Our studies demonstrated an important role for PGE(2) and its EP(4) receptor in the promotion of mucosal proliferation. However, whether β-arrestin1 (β-arr1), a well-established mediator of GPCRs, is involved in the PGE(2) /EP(4) receptor-mediated mucosal proliferation complex in PHG remains unclear. The aim of the study was to investigate whether β-arr1 participated in PGE(2) /EP(4) receptor-mediated mucosal proliferation by recruiting the Src/EGF receptor (EGFR) complex to activate Akt/proliferating cell nuclear antigen (PCNA) signalling in PHG. EXPERIMENTAL APPROACH: Gastric mucosal proliferation was examined in patients with PHG and the PHG model of β-arr1-knockout (β-arr1-KO) and β-arr1-wild type (β-arr1-WT) mice. The induction of β-arr1 and EP(4) receptor expression and the Src/EGFR signalling elements was investigated, and the mechanisms underlying PGE(2) -regulated gastric mucosal proliferation were analysed. KEY RESULTS: Portal hypertension suppressed COX-1 but not COX-2, which was accompanied by a down-regulation of PGE(2) generation and EP(4) receptor levels in the mucosa of patients with PHG. PGE(2) administration markedly promoted mucosal proliferation in a mouse model of PHG. Targeted deletion of β-arr1 abolished PGE(2) /EP(4) receptor-mediated gastric proliferation in PHG by repressing the Src/EGFR/Akt/PCNA signalling network. CONCLUSIONS AND IMPLICATIONS: These results indicate that β-arr1 regulates PGE(2) /EP(4) receptor-mediated mucosal proliferation by promoting activation of the Src/EGFR/Akt/PCNA signalling pathway, and thus, this network is a potential therapeutic target for PHG.