Literature DB >> 17516461

An in vivo look at vertebrate liver architecture: three-dimensional reconstructions from medaka (Oryzias latipes).

Ron C Hardman1, Dave C Volz, Seth W Kullman, David E Hinton.   

Abstract

Understanding three-dimensional (3D) hepatobiliary architecture is fundamental to elucidating structure/function relationships relevant to hepatobiliary metabolism, transport, and toxicity. To date, factual information on vertebrate liver architecture in 3 dimensions has remained limited. Applying noninvasive in vivo imaging to a living small fish animal model we elucidated, and present here, the 3D architecture of this lower vertebrate liver. Our investigations show that hepatobiliary architecture in medaka is based on a polyhedral (hexagonal) structural motif, that the intrahepatic biliary system is an interconnected network of canaliculi and bile-preductules, and that parenchymal architecture in this lower vertebrate is more related to that of the mammalian liver than previously believed. The in vivo findings presented advance our comparative 3D understanding of vertebrate liver structure/function, help clarify previous discrepancies among vertebrate liver conceptual models, and pose interesting questions regarding the "functional unit" of the vertebrate liver. (c) 2007 Wiley-Liss, Inc.

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Year:  2007        PMID: 17516461     DOI: 10.1002/ar.20524

Source DB:  PubMed          Journal:  Anat Rec (Hoboken)        ISSN: 1932-8486            Impact factor:   2.064


  19 in total

1.  Use of medaka in toxicity testing.

Authors:  Stephanie Padilla; John Cowden; David E Hinton; Bonny Yuen; Sheran Law; Seth W Kullman; Rodney Johnson; Ronald C Hardman; Kevin Flynn; Doris W T Au
Journal:  Curr Protoc Toxicol       Date:  2009-02

2.  Two farnesoid X receptor alpha isoforms in Japanese medaka (Oryzias latipes) are differentially activated in vitro.

Authors:  Deanna L Howarth; Lee R Hagey; Sheran H W Law; Ni Ai; Matthew D Krasowski; Sean Ekins; John T Moore; Erin M Kollitz; David E Hinton; Seth W Kullman
Journal:  Aquat Toxicol       Date:  2010-03-01       Impact factor: 4.964

Review 3.  Zebrafish: an important tool for liver disease research.

Authors:  Wolfram Goessling; Kirsten C Sadler
Journal:  Gastroenterology       Date:  2015-08-28       Impact factor: 22.682

Review 4.  Hepatocyte polarity.

Authors:  Aleksandr Treyer; Anne Müsch
Journal:  Compr Physiol       Date:  2013-01       Impact factor: 9.090

Review 5.  Zebrafish models of human liver development and disease.

Authors:  Benjamin J Wilkins; Michael Pack
Journal:  Compr Physiol       Date:  2013-07       Impact factor: 9.090

Review 6.  Liver Progenitors and Adult Cell Plasticity in Hepatic Injury and Repair: Knowns and Unknowns.

Authors:  Sungjin Ko; Jacquelyn O Russell; Laura M Molina; Satdarshan P Monga
Journal:  Annu Rev Pathol       Date:  2019-08-09       Impact factor: 23.472

7.  Exposure to the synthetic FXR agonist GW4064 causes alterations in gene expression and sublethal hepatotoxicity in eleutheroembryo medaka (Oryzias latipes).

Authors:  Deanna L Howarth; Sheran H W Law; J McHugh Law; J A Mondon; Seth W Kullman; David E Hinton
Journal:  Toxicol Appl Pharmacol       Date:  2009-12-03       Impact factor: 4.219

8.  Antagonistic interaction between Wnt and Notch activity modulates the regenerative capacity of a zebrafish fibrotic liver model.

Authors:  Mianbo Huang; Angela Chang; Minna Choi; David Zhou; Frank A Anania; Chong Hyun Shin
Journal:  Hepatology       Date:  2014-09-10       Impact factor: 17.425

Review 9.  New school in liver development: lessons from zebrafish.

Authors:  Jaime Chu; Kirsten C Sadler
Journal:  Hepatology       Date:  2009-11       Impact factor: 17.425

10.  Non invasive high resolution in vivo imaging of alpha-naphthylisothiocyanate (ANIT) induced hepatobiliary toxicity in STII medaka.

Authors:  Ron Hardman; Seth Kullman; Bonny Yuen; David E Hinton
Journal:  Aquat Toxicol       Date:  2007-10-06       Impact factor: 4.964

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