Abstract

Milk fat globule-EGF factor 8 (MFG-E8) is a secreted glycoprotein that regulates tissue homeostasis, possesses potent anti-inflammatory properties, and protects against tissue injury. The human pancreas expresses MFG-E8; however, the role of MFG-E8 in the pancreas remains unclear. We examined the expression of MFG-E8 in the pancreas at baseline and during cerulein-induced acute pancreatitis in mice and determined whether MFG-E8 attenuates the progression of pancreatitis, a serious inflammatory condition that can be life-threatening. We administered cerulein to wild-type (WT) and Mfge8 knockout (KO) mice to induce pancreatitis. Immunoblot analysis showed that MFG-E8 is constitutively expressed in the murine pancreas and is increased in mice with cerulein-induced acute pancreatitis. In situ hybridization revealed that ductal epithelial cells in the mouse pancreas express Mfge8 transcripts at baseline. During pancreatitis, Mfge8 transcripts were abundantly expressed in acinar cells and endothelial cells in addition to ductal epithelial cells. Knocking out Mfge8 in mice exacerbated the severity of cerulein-induced acute pancreatitis and delayed its resolution. In contrast, administration of recombinant MFG-E8 attenuated cerulein-induced acute pancreatitis and promoted repair of pancreatic injury in Mfge8 KO mice. Taken together, our study suggests that MFG-E8 protects the pancreas against inflammatory injury and promotes pancreatic tissue repair. MFG-E8 may represent a novel therapeutic target in acute pancreatitis.

Highlights

  • Acute pancreatitis is an inflammatory process of the pancreas [1,2]

  • Milk fat globule-EGF factor 8 (MFG-E8) Expression Is Increased in the Exocrine Cellular Compartment of Mouse Pancreas during Cerulein-Induced Acute Pancreatitis

  • We found that MFG-E8 is constitutively expressed in ductal epithelial cells in the murine pancreas

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Summary

Introduction

Acute pancreatitis is an inflammatory process of the pancreas [1,2]. Supportive care is the primary treatment for acute pancreatitis [5,6]. During the past ten years, investigators have revealed several novel potential therapeutic targets in experimental models of pancreatitis. The neuronal guidance protein, netrin-1, has been shown to have anti-inflammatory effects in mice with severe acute pancreatitis [7]. Sakuma et al showed that the chemokine CXCL16 mediates acinar cell necrosis in cerulein-induced acute pancreatitis in mice [11]. Together, these advances have shed new light on the potential for targeted prevention and treatment of acute pancreatitis

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