Literature DB >> 17243141

The straw that stirs the drink: insight into the pathogenesis of inflammatory bowel disease revealed through the study of microflora-induced inflammation in genetically modified mice.

Bruce H Horwitz1.   

Abstract

Abnormal response to enteric microflora is a critical factor driving bowel inflammation in patients with inflammatory bowel disease (IBD). Mice with genetically engineered mutations have played a central role in both formulating this hypothesis and elucidating the mechanism that normally protect the host from excessive inflammation within the bowel. One emerging theme is the importance of regulation within the innate immune system in protecting from microflora-driven pathology. In this review, I describe how genetically engineered mice have played a crucial role in shaping our conceptual understanding of pathways that regulate the development of chronic bowel inflammation, and furthermore, explore data derived from the study of genetically engineered mice that implicates the fundamental importance of regulation within the innate immune system in the control of this process.

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Year:  2007        PMID: 17243141     DOI: 10.1002/ibd.20098

Source DB:  PubMed          Journal:  Inflamm Bowel Dis        ISSN: 1078-0998            Impact factor:   5.325


  7 in total

1.  Systemic macrophage depletion inhibits Helicobacter bilis-induced proinflammatory cytokine-mediated typhlocolitis and impairs bacterial colonization dynamics in a BALB/c Rag2-/- mouse model of inflammatory bowel disease.

Authors:  Sureshkumar Muthupalani; Zhongming Ge; Yan Feng; Barry Rickman; Melissa Mobley; Amanda McCabe; Nico Van Rooijen; James G Fox
Journal:  Infect Immun       Date:  2012-10-01       Impact factor: 3.441

2.  Murine norovirus: an intercurrent variable in a mouse model of bacteria-induced inflammatory bowel disease.

Authors:  Karen Chase Lencioni; Audrey Seamons; Piper M Treuting; Lillian Maggio-Price; Thea Brabb
Journal:  Comp Med       Date:  2008-12       Impact factor: 0.982

3.  Differential mechanisms in the pathogenesis of autoimmune cholangitis versus inflammatory bowel disease in interleukin-2Ralpha(-/-) mice.

Authors:  Willy Hsu; Weici Zhang; Koichi Tsuneyama; Yuki Moritoki; William M Ridgway; Aftab A Ansari; Ross L Coppel; Zhe-Xiong Lian; Ian Mackay; M Eric Gershwin
Journal:  Hepatology       Date:  2009-01       Impact factor: 17.425

Review 4.  Microbial and histopathologic considerations in the use of mouse models of inflammatory bowel diseases.

Authors:  Trenton R Schoeb; Daniel C Bullard
Journal:  Inflamm Bowel Dis       Date:  2012-01-31       Impact factor: 5.325

5.  Disease severity and mortality can be independently regulated in a mouse model of experimental graft versus host disease.

Authors:  Rômulo G Galvani; Ramon Lemos; Rômulo B Areal; Pollyanna A Salvador; Dario S Zamboni; João Luiz M Wanderley; Adriana Bonomo
Journal:  PLoS One       Date:  2015-02-02       Impact factor: 3.240

6.  An antibiotic-responsive mouse model of fulminant ulcerative colitis.

Authors:  Silvia S Kang; Seth M Bloom; Lyse A Norian; Michael J Geske; Richard A Flavell; Thaddeus S Stappenbeck; Paul M Allen
Journal:  PLoS Med       Date:  2008-03-04       Impact factor: 11.069

7.  Carrageenan Gum and Adherent Invasive Escherichia coli in a Piglet Model of Inflammatory Bowel Disease: Impact on Intestinal Mucosa-associated Microbiota.

Authors:  Peris M Munyaka; Shadi Sepehri; Jean-Eric Ghia; Ehsan Khafipour
Journal:  Front Microbiol       Date:  2016-04-05       Impact factor: 5.640

  7 in total

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