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Gastrointestinal Physiology and Diseases

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Cover of 'Gastrointestinal Physiology and Diseases'

Table of Contents

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    Book Overview
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    Chapter 1 CRISPR/Cas9-Mediated Genome Editing of Mouse Small Intestinal Organoids.
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    Chapter 2 Lentivirus-Based Stable Gene Delivery into Intestinal Organoids.
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    Chapter 3 Co-culture of Gastric Organoids and Immortalized Stomach Mesenchymal Cells.
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    Chapter 4 An Air-Liquid Interface Culture System for 3D Organoid Culture of Diverse Primary Gastrointestinal Tissues.
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    Chapter 5 Organotypical Tissue Cultures from Fetal and Neonatal Murine Colon.
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    Chapter 6 Ussing Chamber Technique to Measure Intestinal Epithelial Permeability.
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    Chapter 7 HPLC-Based Metabolomic Analysis of Normal and Inflamed Gut.
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    Chapter 8 Gastrointestinal Physiology and Diseases
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    Chapter 9 Gastrointestinal Physiology and Diseases
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    Chapter 10 Gastrointestinal Physiology and Diseases
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    Chapter 11 Gastrointestinal Physiology and Diseases
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    Chapter 12 Label-Free Imaging of Eosinophilic Esophagitis Mouse Models Using Optical Coherence Tomography.
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    Chapter 13 Near-Infrared Fluorescence Endoscopy to Detect Dysplastic Lesions in the Mouse Colon.
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    Chapter 14 Visualization of Signaling Molecules During Neutrophil Recruitment in Transgenic Mice Expressing FRET Biosensors.
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    Chapter 15 In Vivo Myeloperoxidase Imaging and Flow Cytometry Analysis of Intestinal Myeloid Cells.
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    Chapter 16 Gastrointestinal Physiology and Diseases
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    Chapter 17 Gastrointestinal Physiology and Diseases
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    Chapter 18 Purification and Adoptive Transfer of Group 3 Gut Innate Lymphoid Cells.
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    Chapter 19 Immunotherapy with iTreg and nTreg Cells in a Murine Model of Inflammatory Bowel Disease.
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    Chapter 20 Gastrointestinal Physiology and Diseases
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    Chapter 21 Investigation of Host and Pathogen Contributions to Infectious Colitis Using the Citrobacter rodentium Mouse Model of Infection.
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    Chapter 22 Gastrointestinal Physiology and Diseases
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    Chapter 23 Oxazolone-Induced Colitis as a Model of Th2 Immune Responses in the Intestinal Mucosa.
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    Chapter 24 The Mongolian Gerbil: A Robust Model of Helicobacter pylori-Induced Gastric Inflammation and Cancer.
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    Chapter 25 A Rapid Screenable Assay for Compounds That Protect Against Intestinal Injury in Zebrafish Larva.
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    Chapter 26 AOM/DSS Model of Colitis-Associated Cancer.
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    Chapter 27 Characterization of Colorectal Cancer Development in Apc (min/+) Mice.
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    Chapter 28 Modeling Murine Gastric Metaplasia Through Tamoxifen-Induced Acute Parietal Cell Loss.
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    Chapter 29 The Hamster Buccal Pouch Model of Oral Carcinogenesis.
Attention for Chapter 14: Visualization of Signaling Molecules During Neutrophil Recruitment in Transgenic Mice Expressing FRET Biosensors.
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Chapter title
Visualization of Signaling Molecules During Neutrophil Recruitment in Transgenic Mice Expressing FRET Biosensors.
Chapter number 14
Book title
Gastrointestinal Physiology and Diseases
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3603-8_14
Pubmed ID
Book ISBNs
978-1-4939-3601-4, 978-1-4939-3603-8
Authors

Rei Mizuno, Yuji Kamioka, Yoshiharu Sakai, Michiyuki Matsuda, Mizuno, Rei, Kamioka, Yuji, Sakai, Yoshiharu, Matsuda, Michiyuki

Editors

Andrei I. Ivanov

Abstract

A number of chemical mediators regulate neutrophil recruitment to inflammatory sites either positively or negatively. Although the actions of each chemical mediator on the intracellular signaling networks controlling cell migration have been studied with neutrophils cultured in vitro, how such chemical mediators act cooperatively or counteractively in vivo remains largely unknown. To understand the mechanisms regulating neutrophil recruitment to the inflamed intestine in vivo, we recently generated transgenic mice expressing biosensors based on FRET (Förster resonance energy transfer) and set up two-photon excitation microscopy to observe the gastrointestinal tract in living mice. By measuring FRET in neutrophils, we showed activity changes of protein kinases in the neutrophils recruited to inflamed intestines. In this chapter, we describe the protocol used to visualize the protein kinase activities in neutrophils of the inflamed intestine of transgenic mice expressing the FRET biosensors.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 7 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 7 100%

Demographic breakdown

Readers by professional status Count As %
Student > Doctoral Student 1 14%
Professor 1 14%
Student > Master 1 14%
Researcher 1 14%
Professor > Associate Professor 1 14%
Other 0 0%
Unknown 2 29%
Readers by discipline Count As %
Agricultural and Biological Sciences 3 43%
Chemistry 1 14%
Unknown 3 43%