Literature DB >> 16530524

Loss of the major duodenal papilla results in brown pigment biliary stone formation in pdx1 null mice.

Akihisa Fukuda1, Yoshiya Kawaguchi, Kenichiro Furuyama, Sota Kodama, Takeshi Kuhara, Masashi Horiguchi, Masayuki Koizumi, Koji Fujimoto, Ryuichiro Doi, Christopher V E Wright, Tsutomu Chiba.   

Abstract

BACKGROUND & AIMS: Pdx1 plays a pivotal role in pancreas organogenesis and specification of some types of cells in the duodenum and antral stomach. However, its expression is not restricted to pancreas, duodenum, and antral stomach but is also found in the common bile duct during embryogenesis. This study aimed to elucidate the role of Pdx1 in the development of the common bile duct, major duodenal papilla, and duodenum.
METHODS: Expression pattern of pdx1 during embryogenesis and the morphology of the common bile duct, major duodenal papilla, and duodenum in pdx1 null mice were analyzed.
RESULTS: The major duodenal papilla, peribiliary glands, and mucin-producing cells in the common bile duct were not formed in pdx1 null mice. Pdx1 null mice had shorter periampullary duodenal villi than wild-type mice at postnatal stages associated with reduced cell proliferation and increased apoptosis of the duodenal epithelial cells. Loss of the major duodenal papilla allowed duodeno-biliary reflux and bile infection, resulting in the formation of brown pigment biliary stones in pdx1 null mice, and antibiotics treatment significantly reduced the incidence of biliary stone formation.
CONCLUSIONS: Pdx1 is required for proper development of the major duodenal papilla, peribiliary glands, and mucin-producing cells in the common bile duct and for maintenance of the periampullary duodenal epithelial cells during perinatal period. Bile infection because of loss of the major duodenal papilla plays a significant role in the formation of brown pigment biliary stones in pdx1 null mice.

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Year:  2006        PMID: 16530524     DOI: 10.1053/j.gastro.2005.11.031

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   22.682


  8 in total

1.  Ectopic pancreas formation in Hes1 -knockout mice reveals plasticity of endodermal progenitors of the gut, bile duct, and pancreas.

Authors:  Akihisa Fukuda; Yoshiya Kawaguchi; Kenichiro Furuyama; Sota Kodama; Masashi Horiguchi; Takeshi Kuhara; Masayuki Koizumi; Daniel F Boyer; Koji Fujimoto; Ryuichiro Doi; Ryoichiro Kageyama; Christopher V E Wright; Tsutomu Chiba
Journal:  J Clin Invest       Date:  2006-05-18       Impact factor: 14.808

2.  Pdx-1 and Ptf1a concurrently determine fate specification of pancreatic multipotent progenitor cells.

Authors:  Jared S Burlison; Qiaoming Long; Yoshio Fujitani; Christopher V E Wright; Mark A Magnuson
Journal:  Dev Biol       Date:  2008-01-26       Impact factor: 3.582

3.  Directed differentiation of progenitor cells towards an islet-cell phenotype.

Authors:  Arif Abed; Charlotte Critchlow; Peter R Flatt; Neville H McClenaghan; Catriona Kelly
Journal:  Am J Stem Cells       Date:  2012-11-30

4.  Biliary Microbiota in Choledocholithiasis and Correlation With Duodenal Microbiota.

Authors:  Jinyan Han; Shuodong Wu; Ying Fan; Yu Tian; Jing Kong
Journal:  Front Cell Infect Microbiol       Date:  2021-04-29       Impact factor: 5.293

Review 5.  Mechanisms of embryonic stomach development.

Authors:  Kyle W McCracken; James M Wells
Journal:  Semin Cell Dev Biol       Date:  2017-02-24       Impact factor: 7.499

Review 6.  Development of the bile ducts: essentials for the clinical hepatologist.

Authors:  Mario Strazzabosco; Luca Fabris
Journal:  J Hepatol       Date:  2012-01-13       Impact factor: 25.083

7.  Reduction of Ptf1a gene dosage causes pancreatic hypoplasia and diabetes in mice.

Authors:  Akihisa Fukuda; Yoshiya Kawaguchi; Kenichiro Furuyama; Sota Kodama; Masashi Horiguchi; Takeshi Kuhara; Michiya Kawaguchi; Mami Terao; Ryuichiro Doi; Christopher V E Wright; Mikio Hoshino; Tsutomu Chiba; Shinji Uemoto
Journal:  Diabetes       Date:  2008-06-30       Impact factor: 9.461

8.  Diabetes Caused by Elastase-Cre-Mediated Pdx1 Inactivation in Mice.

Authors:  Sota Kodama; Yasuhiro Nakano; Koji Hirata; Kenichiro Furuyama; Masashi Horiguchi; Takeshi Kuhara; Toshihiko Masui; Michiya Kawaguchi; Maureen Gannon; Christopher V E Wright; Shinji Uemoto; Yoshiya Kawaguchi
Journal:  Sci Rep       Date:  2016-02-18       Impact factor: 4.379

  8 in total

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