Ethanol inhibits pancreatic acinar cell autophagy through upregulation of ATG4B, mediating pathological responses of alcoholic pancreatitis

Author:

Mareninova Olga A.123ORCID,Gretler Sophie R.123,Lee Grace E.1,Pimienta Michael1,Qin Yueqiu14,Elperin Jason M.1,Ni Jinliang15,Razga Zsolt6,Gukovskaya Anna S.123ORCID,Gukovsky Ilya123ORCID

Affiliation:

1. David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California, United States

2. Veterans Affairs Greater Los Angeles Healthcare System, Los Angeles, California, United States

3. Southern California Research Center for Alcoholic Liver and Pancreatic Diseases and Cirrhosis, Los Angeles, California, United States

4. Division of Gastroenterology and Hepatology, Youjiang Medical University for Nationalities, Baise, China

5. First Affiliated Hospital, Nanjing Medical University, Nanjing, China

6. Institute of Pathology, University of Szeged, Szeged, Hungary

Abstract

Ethanol sensitizes mice and humans to pancreatitis, but the underlying mechanisms remain obscure. Autophagy is important for maintaining pancreatic acinar cell homeostasis, and its impairment drives pancreatitis. This study reveals a novel mechanism, whereby ethanol inhibits autophagosome formation through upregulating ATG4B, a key cysteine protease. ATG4B upregulation inhibits autophagy in acinar cells and aggravates pathological responses of experimental alcoholic pancreatitis. Enhancing pancreatic autophagy, particularly by down-regulating ATG4B, could be beneficial for treatment of alcoholic pancreatitis.

Funder

HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases

HHS | NIH | National Institute on Alcohol Abuse and Alcoholism

U.S. Department of Veterans Affairs

Publisher

American Physiological Society

Subject

Physiology (medical),Gastroenterology,Hepatology,Physiology

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