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Impaired autophagic flux mediates acinar cell vacuole formation and trypsinogen activation in rodent models of acute pancreatitis
Olga A. Mareninova, Kip Hermann, Samuel W. French, Mark S. O’Konski, Stephen J. Pandol, Paul Webster, Ann H. Erickson, Nobuhiko Katunuma, Fred S. Gorelick, Ilya Gukovsky, Anna S. Gukovskaya
Olga A. Mareninova, Kip Hermann, Samuel W. French, Mark S. O’Konski, Stephen J. Pandol, Paul Webster, Ann H. Erickson, Nobuhiko Katunuma, Fred S. Gorelick, Ilya Gukovsky, Anna S. Gukovskaya
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Research Article Gastroenterology

Impaired autophagic flux mediates acinar cell vacuole formation and trypsinogen activation in rodent models of acute pancreatitis

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Abstract

The pathogenic mechanisms underlying acute pancreatitis are not clear. Two key pathologic acinar cell responses of this disease are vacuole accumulation and trypsinogen activation. We show here that both result from defective autophagy, by comparing the autophagic responses in rodent models of acute pancreatitis to physiologic autophagy triggered by fasting. Pancreatitis-induced vacuoles in acinar cells were greater in number and much larger than those induced with fasting. Degradation of long-lived proteins, a measure of autophagic efficiency, was markedly inhibited in in vitro pancreatitis, while it was stimulated by acinar cell starvation. Further, processing of the lysosomal proteases cathepsin L (CatL) and CatB into their fully active, mature forms was reduced in pancreatitis, as were their activities in the lysosome-enriched subcellular fraction. These findings indicate that autophagy is retarded in pancreatitis due to deficient lysosomal degradation caused by impaired cathepsin processing. Trypsinogen activation occurred in pancreatitis but not with fasting and was prevented by inhibiting autophagy. A marker of trypsinogen activation partially localized to autophagic vacuoles, and pharmacologic inhibition of CatL increased the amount of active trypsin in acinar cells. The results suggest that retarded autophagy is associated with an imbalance between CatL, which degrades trypsinogen and trypsin, and CatB, which converts trypsinogen into trypsin, resulting in intra-acinar accumulation of active trypsin in pancreatitis. Thus, deficient lysosomal degradation may be a dominant mechanism for increased intra-acinar trypsin in pancreatitis.

Authors

Olga A. Mareninova, Kip Hermann, Samuel W. French, Mark S. O’Konski, Stephen J. Pandol, Paul Webster, Ann H. Erickson, Nobuhiko Katunuma, Fred S. Gorelick, Ilya Gukovsky, Anna S. Gukovskaya

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Figure 4

In pancreatitis, lysosomal markers accumulate in a heavier, ZG-enriched subcellular fraction.

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In pancreatitis, lysosomal markers accumulate in a heavier, ZG-enriched ...
(A and B) Characterization of pancreatic tissue subcellular fractions. Rat pancreas homogenate was fractionated by differential centrifugation, as described in Methods, to obtain 1,300-g pellet enriched in ZGs (fraction Z [Z]); 12,000-g pellet enriched in lysosomes (fraction L [L]); and 12,000-g supernatant containing early endosomes and cytosolic proteins (fraction E [E]). (A) The indicated subcellular fractions were analyzed under electron microscope or under fluorescence microscope using the lysosomal vital stain LysoTracker Red. Original magnification: ×7,500 (left panel); ×12,500 (center panel); ×40 (right panel). Larger EM fields are shown in the Supplemental Figure 3. (B) Subcellular fractions from normal rat pancreas were analyzed by immunoblot using antibodies against proteins specific for the organelles listed to the right. COX IV, cytochrome c oxidase subunit IV; PDI, protein disulfide isomerase; EEA1, early endosomal antigen. (C and E) Rats were subjected to conditions of fasting and pancreatitis induced by CR or Arg, as described in Methods. The levels of LC3-II, Rab7, LAMP-1, and LAMP-2 were measured by immunoblot in pancreatic tissue subcellular fractions. For each protein, the same amount of protein was loaded in all samples. The data are representative of several immunoblots from at least 3 rats for each condition. (D) Colocalization of the autophagic marker LC3 with amylase in fraction Z, obtained from a rat with CR pancreatitis, was determined by double staining with anti-LC3 antibody and FITC-conjugated secondary antibody (for LC3 dots) and with amylase antibody and Texas Red–conjugated secondary antibody. Original magnification: ×63.

Copyright © 2026 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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