Document Detail


Impaired autophagy underlies key pathological responses of acute pancreatitis.
MedLine Citation:
PMID:  20215882     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The main function of the exocrine pancreas is to produce digestive enzymes, which normally are secreted as inactive zymogens and become activated after reaching the duodenum. Pancreatitis is a relatively common and potentially fatal inflammatory disease of the exocrine pancreas. Its mild forms are self-limited, but severe pancreatitis has 10%-30% mortality. The pathogenesis of pancreatitis remains obscure, and there are no specific treatments. The disease is believed to initiate in acinar cells, the main cell type of the exocrine pancreas. Hallmark responses of acute pancreatitis are the premature, intra-acinar cell activation of trypsinogen (i.e., its conversion from zymogen to active trypsin), vacuole accumulation, inflammation and death of acinar cells through both necrosis and apoptosis.
Authors:
Ilya Gukovsky; Anna S Gukovskaya
Publication Detail:
Type:  Journal Article     Date:  2010-04-15
Journal Detail:
Title:  Autophagy     Volume:  6     ISSN:  1554-8635     ISO Abbreviation:  Autophagy     Publication Date:  2010 Apr 
Date Detail:
Created Date:  2010-04-23     Completed Date:  2010-08-12     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101265188     Medline TA:  Autophagy     Country:  United States    
Other Details:
Languages:  eng     Pagination:  428-9     Citation Subset:  IM    
Affiliation:
VA Greater Los Angeles Healthcare System and University of California, Los Angeles, Los Angeles, CA, USA. igukovsk@ucla.edu
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MeSH Terms
Descriptor/Qualifier:
Autophagy / physiology*
Cathepsin B / metabolism
Humans
Lysosomes / metabolism
Pancreatitis, Acute Necrotizing / mortality,  pathology*,  physiopathology
Trypsin / metabolism
Vacuoles / metabolism
Chemical
Reg. No./Substance:
EC 3.4.21.4/Trypsin; EC 3.4.22.1/Cathepsin B

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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