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Somatic Stem Cells

Overview of attention for book
Cover of 'Somatic Stem Cells'

Table of Contents

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    Book Overview
  2. Altmetric Badge
    Chapter 1 An Update on the Therapeutic Potential of Stem Cells
  3. Altmetric Badge
    Chapter 2 Single-Step Plasmid Based Reprogramming of Human Dermal Fibroblasts to Induced Neural Stem Cells
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    Chapter 3 Isolation and Analysis of Mesenchymal Progenitors of the Adult Hematopoietic Niche
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    Chapter 4 Identification and Isolation of Mice and Human Hematopoietic Stem Cells
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    Chapter 5 Identification and Characterization of Hair Follicle Stem Cells
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    Chapter 6 Methods of Mesenchymal Stem Cell Homing to the Blood–Brain Barrier
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    Chapter 7 3D Bioprinting and Stem Cells
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    Chapter 8 Characterization of Gastrospheres Using 3D Coculture System
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    Chapter 9 Markers and Methods to Study Adult Midgut Stem Cells
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    Chapter 10 Quantitative Analysis of Intestinal Stem Cell Dynamics Using Microfabricated Cell Culture Arrays
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    Chapter 11 Detection, Labeling, and Culture of Lung Stem and Progenitor Cells
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    Chapter 12 Isolation, Characterization and Differentiation of Mouse Cardiac Progenitor Cells
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    Chapter 13 Isolating and Characterizing Adipose-Derived Stem Cells
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    Chapter 14 Enzyme-Free Isolation of Adipose-Derived Mesenchymal Stem Cells
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    Chapter 15 Identification and Characterizations of Annulus Fibrosus-Derived Stem Cells
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    Chapter 16 Maintenance of Tendon Stem/Progenitor Cells in Culture
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    Chapter 17 Intravital Imaging to Understand Spatiotemporal Regulation of Osteogenesis and Angiogenesis in Cranial Defect Repair and Regeneration
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    Chapter 18 Beating Heart Cells from Hair-Follicle-Associated Pluripotent (HAP) Stem Cells
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    Chapter 19 Generation of FLIP and FLIP-FlpE Targeting Vectors for Biallelic Conditional and Reversible Gene Knockouts in Mouse and Human Cells
  21. Altmetric Badge
    Chapter 20 Analytical Platforms and Techniques to Study Stem Cell Metabolism
Attention for Chapter 8: Characterization of Gastrospheres Using 3D Coculture System
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Chapter title
Characterization of Gastrospheres Using 3D Coculture System
Chapter number 8
Book title
Somatic Stem Cells
Published in
Methods in molecular biology, September 2018
DOI 10.1007/978-1-4939-8697-2_8
Pubmed ID
Book ISBNs
978-1-4939-8696-5, 978-1-4939-8697-2
Authors

Carlos Antônio do Nascimento Santos, Radovan Borojevic, Luiz Eurico Nasciutti, Christina M. Maedatakiya, Nascimento Santos, Carlos Antônio do, Borojevic, Radovan, Nasciutti, Luiz Eurico, Maedatakiya, Christina M.

Abstract

To understand the molecular mechanisms involved in gastric disorders and regeneration, we need an in vitro tridimensional (3D) culture model, which can mimic the in vivo gastric microenvironment. A 3D coculture system named gastrosphere is proposed herein, composed of primary human gastric epithelial and stromal cells. The primary cultures were obtained from endoscopic gastric biopsies, and after mechanical and enzymatic dispersion, epithelial (HGE3) and stromal (HGS12) cells were expanded. After extensive immunocytochemical characterization, cells were seeded onto 96-well round bottom plates previously covered with 1% agarose. Cells were cultured in KM-F12 culture medium with 10% fetal bovine serum (FBS), antibiotics, and antimycotics, in humidified air at 37 °C and atmosphere containing 5% CO2 for 72 h or until spheres formation. Then gastrospheres were carefully transferred to a rotary cell culture system (RCCS-4), and maintained for 07, 14, 21, and 28 days. Gastrospheres were morphologically characterized by immunocytochemistry [cytokeratins (CK), vimentin, α-smooth muscle actin (α-SMA), laminin (LN), fibronectin (FN), and type IV collagen (CIV), proliferating cell nuclear antigen (PCNA)], and electron microscopy. In gastrospheres, the cytokeratin-positive epithelial cells were found in the outer layer, while vimentin-positive stromal cells were localized in the center of the gastrospheres. PCNA+ cells were mainly seen at the peripheral and in the intermediary region while nestin+ cells were also depicted in the latter zone. Scanning electron microscopy revealed groups of cohesive gastric cells at the periphery, while transmission electron microscopy demonstrated some differentiated mucous-like or zymogenic-like cells in the periphery and stromal structures located at the center of the 3D structures. Extracellular matrix was deposed between cells. Our data suggest that in vitro gastrospheres recapitulate the in vivo gastric microenvironment.

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Mendeley readers

The data shown below were compiled from readership statistics for 5 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 5 100%

Demographic breakdown

Readers by professional status Count As %
Professor 1 20%
Student > Ph. D. Student 1 20%
Student > Postgraduate 1 20%
Unknown 2 40%
Readers by discipline Count As %
Medicine and Dentistry 2 40%
Social Sciences 1 20%
Biochemistry, Genetics and Molecular Biology 1 20%
Unknown 1 20%