EBioMedicine
(Oct 2017)
Transcriptome Analysis Uncovers a Growth-Promoting Activity of Orosomucoid-1 on Hepatocytes
Xian-Yang Qin,
Mitsuko Hara,
Erik Arner,
Yoshikuni Kawaguchi,
Ikuyo Inoue,
Hideki Tatsukawa,
Yutaka Furutani,
Keisuke Nagatsuma,
Tomokazu Matsuura,
Feifei Wei,
Jun Kikuchi,
Hideko Sone,
Carsten Daub,
Hideya Kawaji,
Timo Lassmann,
Masayoshi Itoh,
Harukazu Suzuki,
Piero Carninci,
Yoshihide Hayashizaki,
Norihiro Kokudo,
Alistair R.R. Forrest,
Soichi Kojima
Affiliations
Xian-Yang Qin
Micro-Signaling Regulation Technology Unit, RIKEN Center for Life Science Technologies, Wako, Saitama 3510198, Japan
Mitsuko Hara
Micro-Signaling Regulation Technology Unit, RIKEN Center for Life Science Technologies, Wako, Saitama 3510198, Japan
Erik Arner
Division of Genomic Technologies, RIKEN Center for Life Science Technologies, Yokohama, Kanagawa 2300045, Japan
Yoshikuni Kawaguchi
Hepato-Biliary-Pancreatic Surgery Division, Department of Surgery, Graduate School of Medicine, The University of Tokyo, Tokyo 1130033, Japan
Ikuyo Inoue
Micro-Signaling Regulation Technology Unit, RIKEN Center for Life Science Technologies, Wako, Saitama 3510198, Japan
Hideki Tatsukawa
Department of Basic Medicinal Sciences, Nagoya University Graduate School of Pharmaceutical Sciences, Nagoya, Aichi 4648601, Japan
Yutaka Furutani
Micro-Signaling Regulation Technology Unit, RIKEN Center for Life Science Technologies, Wako, Saitama 3510198, Japan
Keisuke Nagatsuma
Department of Laboratory Medicine, The Jikei University School of Medicine, Tokyo 1058461, Japan
Tomokazu Matsuura
Department of Laboratory Medicine, The Jikei University School of Medicine, Tokyo 1058461, Japan
Feifei Wei
Metabolomics Research Group, RIKEN Center for Sustainable Resource Science, Yokohama, Kanagawa 2300045, Japan
Jun Kikuchi
Metabolomics Research Group, RIKEN Center for Sustainable Resource Science, Yokohama, Kanagawa 2300045, Japan
Hideko Sone
Center for Health and Environmental Risk Research, National Institute for Environmental Studies, Tsukuba, Ibaraki 3058606, Japan
Carsten Daub
Division of Genomic Technologies, RIKEN Center for Life Science Technologies, Yokohama, Kanagawa 2300045, Japan
Hideya Kawaji
Division of Genomic Technologies, RIKEN Center for Life Science Technologies, Yokohama, Kanagawa 2300045, Japan
Timo Lassmann
Division of Genomic Technologies, RIKEN Center for Life Science Technologies, Yokohama, Kanagawa 2300045, Japan
Masayoshi Itoh
Division of Genomic Technologies, RIKEN Center for Life Science Technologies, Yokohama, Kanagawa 2300045, Japan
Harukazu Suzuki
Division of Genomic Technologies, RIKEN Center for Life Science Technologies, Yokohama, Kanagawa 2300045, Japan
Piero Carninci
Division of Genomic Technologies, RIKEN Center for Life Science Technologies, Yokohama, Kanagawa 2300045, Japan
Yoshihide Hayashizaki
RIKEN Preventive Medicine and Diagnosis Innovation Program (PMI), Wako, Saitama 3510198, Japan
Norihiro Kokudo
Hepato-Biliary-Pancreatic Surgery Division, Department of Surgery, Graduate School of Medicine, The University of Tokyo, Tokyo 1130033, Japan
Alistair R.R. Forrest
Division of Genomic Technologies, RIKEN Center for Life Science Technologies, Yokohama, Kanagawa 2300045, Japan
Soichi Kojima
Micro-Signaling Regulation Technology Unit, RIKEN Center for Life Science Technologies, Wako, Saitama 3510198, Japan
DOI
https://doi.org/10.1016/j.ebiom.2017.09.008
Journal volume & issue
Vol. 24,
no. C
pp.
257
– 266
Abstract
Read online
The acute phase protein orosomucoid-1 (Orm1) is mainly expressed by hepatocytes (HPCs) under stress conditions. However, its specific function is not fully understood. Here, we report a role of Orm1 as an executer of HPC proliferation. Increases in serum levels of Orm1 were observed in patients after surgical resection for liver cancer and in mice undergone partial hepatectomy (PH). Transcriptome study showed that Orm1 became the most abundant in HPCs isolated from regenerating mouse liver tissues after PH. Both in vitro and in vivo siRNA-induced knockdown of Orm1 suppressed proliferation of mouse regenerating HPCs and human hepatic cells. Microarray analysis in regenerating mouse livers revealed that the signaling pathways controlling chromatin replication, especially the minichromosome maintenance protein complex genes were uniformly down-regulated following Orm1 knockdown. These data suggest that Orm1 is induced in response to hepatic injury and executes liver regeneration by activating cell cycle progression in HPCs.
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