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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 2

Compared with fasting, pancreatitis-induced autophagic vacuoles are greater in number and much larger.

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Compared with fasting, pancreatitis-induced autophagic vacuoles are grea...
(A) LC3-I to LC3-II conversion (immunoblot) in pancreas of rats under conditions of fasting (for 17 hours) and pancreatitis (see Methods). ERK1/2 served as loading control. (B) Colocalization of the autophagy marker LC3 with amylase, a ZG marker, under conditions of fasting and CR pancreatitis. Pancreatic tissue sections were double immunostained for LC3 and amylase. Images were visualized under confocal microscope. Larger boxes show expanded images of the areas indicated by smaller boxes. (C) Effects of fasting and pancreatitis on LC3 dots in pancreas, as shown in B. The number of LC3 dots was normalized to that of nuclei in the same field. (D) Autophagic vacuoles were identified on electron micrographs (see Figure 1), and their size was measured relative to the average size of nuclei on the same micrograph. (E) Acinar cell vacuolation on H&E-stained pancreatic tissue sections from rats under conditions of fasting or CR pancreatitis (original magnification, ×40) and from a patient with acute pancreatitis (a gift from D.S. Longnecker; original magnification, ×60). (F). Cross-sectioned area of pancreas occupied by vacuoles was quantified on H&E-stained sections using MetaMorph 6 software. Values in C, D, and F are (mean ± SEM) from 3–5 rats for each condition. In C and F, at least 1,000 acinar cells were counted for each animal. In D, 20–30 acinar cells from at least 3 rats were counted for each condition. *P < 0.05 versus fed rats; #P < 0.02 versus fasting rats.

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

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