Veterans Affairs Greater Los Angeles Healthcare System and University of California at Los Angeles, Los Angeles, CA 90073, USA.
Am J Physiol Gastrointest Liver Physiol. 2012 Nov 1;303(9):G993-G1003. doi: 10.1152/ajpgi.00122.2012. Epub 2012 Sep 6.
Acute pancreatitis is an inflammatory disease of the exocrine pancreas that carries considerable morbidity and mortality; its pathophysiology remains poorly understood. Recent findings from experimental models and genetically altered mice summarized in this review reveal that autophagy, the principal cellular degradative pathway, is impaired in pancreatitis and that one cause of autophagy impairment is defective function of lysosomes. We propose that the lysosomal/autophagic dysfunction is a key initiating event in pancreatitis and a converging point of multiple deranged pathways. There is strong evidence supporting this hypothesis. Investigation of autophagy in pancreatitis has just started, and many questions about the "upstream" mechanisms mediating the lysosomal/autophagic dysfunction and the "downstream" links to pancreatitis pathologies need to be explored. Answers to these questions should provide insight into novel molecular targets and therapeutic strategies for treatment of pancreatitis.
急性胰腺炎是一种胰腺外分泌的炎症性疾病,具有相当高的发病率和死亡率;其病理生理学仍未被很好地理解。本综述总结了实验模型和基因改变小鼠的最新发现,揭示了自噬,即主要的细胞降解途径,在胰腺炎中受损,自噬受损的一个原因是溶酶体功能缺陷。我们提出,溶酶体/自噬功能障碍是胰腺炎的一个关键起始事件,也是多种紊乱途径的汇聚点。有强有力的证据支持这一假设。对胰腺炎中自噬的研究才刚刚开始,许多关于介导溶酶体/自噬功能障碍的“上游”机制以及与胰腺炎病理的“下游”联系的问题需要探索。这些问题的答案应该为治疗胰腺炎的新的分子靶点和治疗策略提供深入了解。