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Increased expression and altered localization of cathepsin Z are associated with progression to jaundice stage in primary biliary cholangitis

Authors :
Seigo Abiru
Yoshihiro Aiba
Minoru Nakamura
Shinji Shimoda
Takashi Suematsu
Kenichi Harada
Masahiro Ito
Hitomi Nakamura
Nao Nishida
Hiroshi Yatsuhashi
Shinichi Aishima
Katsushi Tokunaga
Kiyoshi Migita
Atsumasa Komori
Minae Kawashima
Yuki Hitomi
Mitsuhisa Takatsuki
Shinya Nagaoka
Susumu Eguchi
Source :
Scientific Reports, Vol 8, Iss 1, Pp 1-11 (2018), Scientific Reports
Publication Year :
2018
Publisher :
Springer Science and Business Media LLC, 2018.

Abstract

Our recent genome-wide association study found that the NELFCD/CTSZ locus was significantly associated with progression of primary biliary cholangitis (PBC) to jaundice stage in the Japanese population. In this study, we investigated the role of cathepsin Z in the etiology and pathology of PBC. Serum cathepsin Z levels were measured using enzyme-linked immunosorbent assay. The expression and localization of cathepsin Z in liver specimens were analyzed by western blotting and immunohistochemistry. In PBC patients, serum cathepsin Z levels were significantly increased with disease progression. In addition, its levels were positively correlated with alanine transaminase, aspartate transaminase and total bilirubin, and were negatively correlated with platelet count and albumin. Cathepsin Z expression was markedly increased in hepatocytes at later stages of PBC, and its localization was altered from the peri-bile canaliculus to the cytoplasm, where a fraction was no longer colocalized with endosomal/lysosomal vesicles. Similar altered expression of cathepsin Z was observed in end-stage of other cholestatic liver diseases including sepsis, obstructive jaundice, and Alagille syndrome. Our results indicate that altered expression and localization of cathepsin Z in hepatocytes are characteristic features of PBC and other cholestatic liver diseases, and are implicated in the progression of PBC.

Details

ISSN :
20452322
Volume :
8
Database :
OpenAIRE
Journal :
Scientific Reports
Accession number :
edsair.doi.dedup.....90e8122fdc6d7e1653cc20f29162711c
Full Text :
https://doi.org/10.1038/s41598-018-30146-w