The fusion of autophagosome with lysosome is impaired in L-arginine-induced acute pancreatitis.

作者：Hongwei Zhu, Xiao Yu, Shaihong Zhu, Xia Li, Ben Lü, Zhiqiang Li, Can Yu · 发表于：PubMed · 年份：2015 · 被引用次数：13 · 研究领域：Pancreatitis Pathology and Treatment、Autophagy in Disease and Therapy、Calcium signaling and nucleotide metabolism

BACKGROUND & AIMS: Acute pancreatitis is an inflammatory pancreatic disease that carries considerable morbidity and mortality. The pathogenesis of this disease remains poorly understood. We investigated the incidence of autophagy in mice following induction of acute pancreatitis. METHODS: Mice were received intraperitoneal injections of L-arginine (200 mg × 2/100 g BW), while controls were administered with saline. Pancreatic tissues were assessed by histology, electron microscopy and western blotting. RESULTS: Injection of L-arginine resulted in the accumulation of autophagosomes and a relative paucity of autolysosomes. Moreover, the autophagy marker p62 is significantly increased. However, the lysosomal-associated membrane protein-2 (Lamp-2), a protein that is required for the proper fusion of autophagosomes with lysosomes, is decreased in acute pancreatitis. These results suggest that a crucial role for autophagy and Lamp-2 in the pathogenesis of acute pancreatitis. CONCLUSIONS: Our data suggest that the autophagic flux is impaired in acute pancreatitis. The depletion of Lamp-2 may play a role in the pathogenesis of acute pancreatitis.