Abnormality of autophagic function and cathepsin expression in the liver from patients with non-alcoholic fatty liver disease

被引:162
作者
Fukuo, Yuka [1 ]
Yamashina, Shunhei [1 ]
Sonoue, Hiroshi [2 ]
Arakawa, Atsushi [2 ]
Nakadera, Eisuke [1 ]
Aoyama, Tomonori [1 ]
Uchiyama, Akira [1 ]
Kon, Kazuyoshi [1 ]
Ikejima, Kenichi [1 ]
Watanabe, Sumio [1 ]
机构
[1] Juntendo Univ, Sch Med, Dept Gastroenterol, Tokyo 113, Japan
[2] Juntendo Univ, Sch Med, Dept Human Pathol, Tokyo 113, Japan
关键词
autophagy; inflammation; p62; steatosis; HEPATITIS-C VIRUS; B-VIRUS; PROTEIN; CELLS; IMPAIRMENT; STRESS; NRF2; P62;
D O I
10.1111/hepr.12282
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AimRecent evidences indicate that hepatic steatosis suppresses autophagic proteolysis. The present study evaluated the correlation between autophagic function and cathepsin expression in the liver from patients with non-alcoholic fatty liver disease (NAFLD). MethodsLiver biopsy specimens were obtained from patients with chronic liver diseases (chronic hepatitis C [CHC; n=20], chronic hepatitis B [CHB; n=16], primary biliary cirrhosis [PBC; n=23], NAFLD [n=22] and control [n=14]). The number of autophagic vesicles in hepatocytes was counted by using transmission electron microscopy. Expression of cathepsin B, D, L and p62 in the liver section was analyzed by immunohistochemical staining. The histological severity of NAFLD is assessed by NAFLD activity score (NAS). ResultsThe number of autophagic vesicles in hepatocytes was significantly increased in both CHC and NAFLD groups, but not CHB and PBC, more than control. Although hepatocytes with aggregation of p62 were observed in less than 15% of CHC, p62 aggregation was detected in approximately 65% of NAFLD. Cathepsin B, D and L expression was significantly suppressed in the liver from NAFLD patients. Suppression of cathepsin B, D and L expression was not observed in CHB, CHC and PBC. In NAFLD patients, p62 aggregation was correlated with serum alanine aminotransferase value and inflammatory activity by NAS. ConclusionThese results indicate that a decrease in hepatic cathepsin expression in NAFLD is associated with autophagic dysfunction. Hepatic inflammation correlates with autophagic dysfunction in NAFLD. These findings indicate that the suppression of autophagic proteolysis by hepatic steatosis is involved in the pathogenesis of NAFLD.
引用
收藏
页码:1026 / 1036
页数:11
相关论文
共 35 条
[1]   Thinking globally and acting locally with TOR [J].
Arsham, Andrew M. ;
Neufeld, Thomas P. .
CURRENT OPINION IN CELL BIOLOGY, 2006, 18 (06) :589-597
[2]   Activity-Based Proteome Profiling of Hepatoma Cells during Hepatitis C Virus Replication Using Protease Substrate Probes [J].
Blais, David R. ;
Brulotte, Marc ;
Qian, Yiming ;
Belanger, Sylvie ;
Yao, Shao Q. ;
Pezacki, John Paul .
JOURNAL OF PROTEOME RESEARCH, 2010, 9 (02) :912-923
[3]   Cysteine cathepsins: Cellular roadmap to different functions [J].
Brix, Klaudia ;
Dunkhorst, Anna ;
Mayer, Kristina ;
Jordans, Silvia .
BIOCHIMIE, 2008, 90 (02) :194-207
[4]   Functions of Autophagy in Hepatic and Pancreatic Physiology and Disease [J].
Czaja, Mark J. .
GASTROENTEROLOGY, 2011, 140 (07) :1895-1908
[5]   Steatohepatitis: A tale of two "hits"? [J].
Day, CP ;
James, OFW .
GASTROENTEROLOGY, 1998, 114 (04) :842-845
[6]  
Dunn William A. Jr., 1994, Trends in Cell Biology, V4, P139, DOI 10.1016/0962-8924(94)90069-8
[7]   BIOSYNTHESIS OF LYSOSOMAL ENDOPEPTIDASES [J].
ERICKSON, AH .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1989, 40 (01) :31-41
[8]   Suppression of autophagy sensitizes Kupffer cells to endotoxin [J].
Fukada, Hiroo ;
Yamashina, Shunhei ;
Izumi, Kousuke ;
Komatsu, Masaaki ;
Tanaka, Keiji ;
Ikejima, Kenichi ;
Watanabe, Sumio .
HEPATOLOGY RESEARCH, 2012, 42 (11) :1112-1118
[9]   Pharmacological therapy of nonalcoholic steatohepatitis [J].
Hojo, Mariko ;
Watanabe, Sumio .
HEPATOLOGY RESEARCH, 2011, 41 (03) :209-216
[10]   Hepatic steatosis inhibits autophagic proteolysis via impairment of autophagosomal acidification and cathepsin expression [J].
Inami, Yoshihiro ;
Yamashina, Shunhei ;
Izumi, Kousuke ;
Ueno, Takashi ;
Tanida, Isei ;
Ikejima, Kenichi ;
Watanabe, Sumio .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2011, 412 (04) :618-625