Abstract

Acute pancreatitis constitutes a life-threatening condition in which pancreatic acinar cells undergo massive cell death. We investigated the incidence of apoptosis, autophagy, and necrosis affecting acinar cells in the early onset of acute pancreatitis induced by chronic alcohol feeding and acute endotoxemia. Rats were fed either an ethanol-containing or a control diet over 14 weeks and killed 3 or 24 hours after a single lipopolysaccharide injection. Apoptosis, necrosis, and autophagy of pancreatic acinar cells were assessed by histology, electron microscopy, immunofluorescence, and biochemical methods. The combination of alcohol exposure and endotoxemia resulted in the depletion of several lysosomal proteins including lysosomal-associated membrane protein-2 (Lamp-2), a protein that is required for the proper fusion of autophagosomes with lysosomes. Accordingly, Lamp-2 depletion correlated with the accumulation of autophagosomes and a relative paucity of autolysosomes, reduced adenosine-5'-triphosphate levels, and a switch from apoptotic to necrotic cell death. This switch to necrosis was accompanied by reduced caspase activation and the nuclear release of the proinflammatory factor high mobility group box 1. Importantly, human patients with alcoholic pancreatitis also exhibited local Lamp-2 depletion, which points to a crucial role for Lamp-2 and autophagy in pancreatic acinar cell death. Our data suggest that acinar cell vacuolization in pancreatitis is mediated by an endotoxemia-induced inhibition of the late stage of autophagy. The combination of alcohol and endotoxemia attenuated apoptosis response yet enhanced acinar cell necrosis. The depletion of lysosomal proteins plays a critical role in the early onset of acute pancreatitis.

Keywords

AutophagyAcinar cellNecrosisProgrammed cell deathApoptosisPancreatitisAcute pancreatitisProinflammatory cytokineEndocrinologyInternal medicineBiologyChemistryCell biologyInflammationMedicineBiochemistry

MeSH Terms

Acute DiseaseAdenosine TriphosphateAnimalsApoptosisAutophagyCaspase 3Caspase 9Cathepsin BCell LineDisease ModelsAnimalDown-RegulationEndotoxemiaEthanolHMGB1 ProteinHumansLipopolysaccharidesLysosomal-Associated Membrane Protein 2Lysosomal Membrane ProteinsLysosomesMaleNecrosisPancreasPancreatitisPancreatitisAlcoholicRNA InterferenceRatsRatsSprague-DawleyTime FactorsTransfectionTrypsin

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Publication Info

Year
2009
Type
article
Volume
137
Issue
1
Pages
350-360.e5
Citations
237
Access
Closed

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237
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Cite This

Franco Fortunato, Heinrich F. Bürgers, Frank Bergmann et al. (2009). Impaired Autolysosome Formation Correlates With Lamp-2 Depletion: Role of Apoptosis, Autophagy, and Necrosis in Pancreatitis. Gastroenterology , 137 (1) , 350-360.e5. https://doi.org/10.1053/j.gastro.2009.04.003

Identifiers

DOI
10.1053/j.gastro.2009.04.003
PMID
19362087

Data Quality

Data completeness: 90%