Differential expression of Lutheran/BCAM regulates biliary tissue remodeling in ductular reaction during liver regeneration

Author:

Miura Yasushi12,Matsui Satoshi13,Miyata Naoko1,Harada Kenichi4,Kikkawa Yamato5,Ohmuraya Masaki6,Araki Kimi7,Tsurusaki Shinya18,Okochi Hitoshi1,Goda Nobuhito2,Miyajima Atsushi3,Tanaka Minoru18ORCID

Affiliation:

1. Department of Regenerative Medicine, Research Institute, National Center for Global Health and Medicine, Tokyo, Japan

2. Department of Life Science and Medical Bioscience, Graduate School of Advanced Science and Engineering, Waseda University, Tokyo, Japan

3. Laboratory of Cell Growth and Differentiation, Institute of Molecular and Cellular Biosciences, The University of Tokyo, Tokyo, Japan

4. Department of Human Pathology, Kanazawa University Graduate School of Medicine, Kanazawa, Japan

5. Department of Clinical Biochemistry, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan

6. Department of Genetics, Hyogo College of Medicine, Hyogo, Japan

7. Institute of Resource Development and Analysis, Kumamoto University, Kumamoto, Japan

8. Laboratory of Stem Cell Regulation, Institute of Molecular and Cellular Biosciences, The University of Tokyo, Tokyo, Japan

Abstract

Under chronic or severe liver injury, liver progenitor cells (LPCs) of biliary origin are known to expand and contribute to the regeneration of hepatocytes and cholangiocytes. This regeneration process is called ductular reaction (DR), which is accompanied by dynamic remodeling of biliary tissue. Although the DR shows apparently distinct mode of biliary extension depending on the type of liver injury, the key regulatory mechanism remains poorly understood. Here, we show that Lutheran (Lu)/Basal cell adhesion molecule (BCAM) regulates the morphogenesis of DR depending on liver disease models. Lu+ and Lu- biliary cells isolated from injured liver exhibit opposite phenotypes in cell motility and duct formation capacities in vitro. By overexpression of Lu, Lu- biliary cells acquire the phenotype of Lu+ biliary cells. Lu-deficient mice showed severe defects in DR. Our findings reveal a critical role of Lu in the control of phenotypic heterogeneity of DR in distinct liver disease models.

Funder

Japan Society for the Promotion of Science

Japan Agency for Medical Research and Development

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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