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3D Cell Culture

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Cover of '3D Cell Culture'

Table of Contents

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    Book Overview
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    Chapter 1 3D Cell Culture: An Introduction
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    Chapter 2 Preparation of Decellularized Biological Scaffolds for 3D Cell Culture
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    Chapter 3 3D Cell Culture in Interpenetrating Networks of Alginate and rBM Matrix
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    Chapter 4 Hydrogel-Based In Vitro Models of Tumor Angiogenesis
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    Chapter 5 Generation of Induced Pluripotent Stem Cells in Defined Three-Dimensional Hydrogels
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    Chapter 6 Calcium Phosphate Foams: Potential Scaffolds for Bone Tissue Modeling in Three Dimensions
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    Chapter 7 Establishment of 3D Intestinal Organoid Cultures from Intestinal Stem Cells
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    Chapter 8 3D Coculture of Mammary Organoids with Fibrospheres: A Model for Studying Epithelial–Stromal Interactions During Mammary Branching Morphogenesis
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    Chapter 9 An Organotypic 3D Assay for Primary Human Mammary Epithelial Cells that Recapitulates Branching Morphogenesis
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    Chapter 10 3D Primary Culture Model to Study Human Mammary Development
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    Chapter 11 Lungosphere Assay: 3D Culture of Lung Epithelial Stem/Progenitor Cells
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    Chapter 12 3D Hanging Drop Culture to Establish Prostate Cancer Organoids
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    Chapter 13 3D-Dynamic Culture Models of Multiple Myeloma
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    Chapter 14 Preparation of a Three-Dimensional Full Thickness Skin Equivalent
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    Chapter 15 Analysis of Breast Cancer Cell Invasion Using an Organotypic Culture System
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    Chapter 16 3D Coculture Model of the Brain Parenchyma–Metastasis Interface of Brain Metastasis
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    Chapter 17 3D Neural Culture in Dual Hydrogel Systems
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    Chapter 18 3D Cell Culture in Micropatterned Hydrogels Prepared by Photomask, Microneedle, or Soft Lithography Techniques
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    Chapter 19 3D Stem Cell Niche Engineering via Two-Photon Laser Polymerization
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    Chapter 20 Microfluidic-Based Generation of 3D Collagen Spheres to Investigate Multicellular Spheroid Invasion
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    Chapter 21 Forecasting smog-related health hazard based on social media and physical sensor
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    Chapter 22 High-Throughput 3D Tumor Culture in a Recyclable Microfluidic Platform
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    Chapter 23 High-Throughput Microfluidic Platform for 3D Cultures of Mesenchymal Stem Cells
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    Chapter 24 3D Anastomosed Microvascular Network Model with Living Capillary Networks and Endothelial Cell-Lined Microfluidic Channels
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    Chapter 25 Human Lung Small Airway-on-a-Chip Protocol
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    Chapter 26 Microfluidic Bioprinting of Heterogeneous 3D Tissue Constructs
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    Chapter 27 Bioprinting of 3D Tissue Models Using Decellularized Extracellular Matrix Bioink
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    Chapter 28 Bioprinting Cartilage Tissue from Mesenchymal Stem Cells and PEG Hydrogel
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    Chapter 29 Real-Time Cell Cycle Imaging in a 3D Cell Culture Model of Melanoma
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    Chapter 30 Revealing 3D Ultrastructure and Morphology of Stem Cell Spheroids by Electron Microscopy
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    Chapter 31 Quantitative Phenotypic Image Analysis of Three-Dimensional Organotypic Cultures
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    Chapter 32 Erratum to: Generation of Induced Pluripotent Stem Cells in Defined Three-Dimensional Hydrogels
Attention for Chapter 7: Establishment of 3D Intestinal Organoid Cultures from Intestinal Stem Cells
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Chapter title
Establishment of 3D Intestinal Organoid Cultures from Intestinal Stem Cells
Chapter number 7
Book title
3D Cell Culture
Published in
Methods in molecular biology, June 2017
DOI 10.1007/978-1-4939-7021-6_7
Pubmed ID
Book ISBNs
978-1-4939-7019-3, 978-1-4939-7021-6
Authors

Shinya Sugimoto, Toshiro Sato M.D., Ph.D., Toshiro Sato

Editors

Zuzana Koledova

Abstract

The intestinal epithelium is the most rapidly renewed tissue in adult mammals, and its renewal is strictly controlled by intestinal stem cells. Extensive studies using genetic models of intestinal epithelium have revealed the mechanisms underlying the self-renewal of intestinal stem cells. Exploiting this knowledge, we developed a novel 3D culture system that enables the outgrowth of intestinal Lgr5(+) stem cells derived from mouse and human tissues into ever-expanding crypt-villus mini-guts, known as intestinal epithelial organoids. These organoids are maintained by the self-renewal of stem cells and give rise to all differentiated cell types of the intestinal epithelium. Once established, organoids can be cryopreserved and thawed when needed. This culture system has been widely used for studying stem cell behavior and gene function and for disease modeling.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 86 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 86 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 17 20%
Student > Bachelor 14 16%
Researcher 12 14%
Student > Master 11 13%
Student > Doctoral Student 5 6%
Other 4 5%
Unknown 23 27%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 29 34%
Immunology and Microbiology 11 13%
Agricultural and Biological Sciences 8 9%
Engineering 4 5%
Medicine and Dentistry 3 3%
Other 2 2%
Unknown 29 34%