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Dendritic Cell Protocols

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Cover of 'Dendritic Cell Protocols'

Table of Contents

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    Book Overview
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    Chapter 1 Review of Mouse and Human Dendritic Cell Subsets.
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    Chapter 2 In Vitro Generation of Human XCR1(+) Dendritic Cells from CD34(+) Hematopoietic Progenitors.
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    Chapter 3 Derivation and Utilization of Functional CD8(+) Dendritic Cell Lines.
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    Chapter 4 Dendritic Cell Protocols
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    Chapter 5 The Isolation and Enrichment of Large Numbers of Highly Purified Mouse Spleen Dendritic Cell Populations and Their In Vitro Equivalents.
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    Chapter 6 Dendritic Cell Subset Purification from Human Tonsils and Lymph Nodes.
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    Chapter 7 Isolation and Identification of Conventional Dendritic Cell Subsets from the Intestine of Mice and Men.
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    Chapter 8 Isolation of Human Skin Dendritic Cell Subsets.
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    Chapter 9 Isolation of Mouse Dendritic Cell Subsets and Macrophages from the Skin.
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    Chapter 10 Isolation of Conventional Dendritic Cells from Mouse Lungs.
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    Chapter 11 Purification of Human Dendritic Cell Subsets from Peripheral Blood.
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    Chapter 12 Protocols for the Identification and Isolation of Antigen-Presenting Cells in Human and Mouse Tissues.
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    Chapter 13 Measurement of Export to the Cytosol in Dendritic Cells Using a Cytofluorimetry-Based Assay.
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    Chapter 14 Dendritic Cell Protocols
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    Chapter 15 Dendritic Cell Protocols
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    Chapter 16 Dendritic Cell Protocols
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    Chapter 17 Dendritic Cell Protocols
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    Chapter 18 Dendritic Cell Protocols
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    Chapter 19 Dendritic Cell Protocols
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    Chapter 20 Dendritic Cell Protocols
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    Chapter 21 Dendritic Cell Protocols
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    Chapter 22 Generation of Humanized Mice for Analysis of Human Dendritic Cells.
Attention for Chapter 22: Generation of Humanized Mice for Analysis of Human Dendritic Cells.
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Chapter title
Generation of Humanized Mice for Analysis of Human Dendritic Cells.
Chapter number 22
Book title
Dendritic Cell Protocols
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3606-9_22
Pubmed ID
Book ISBNs
978-1-4939-3604-5, 978-1-4939-3606-9
Authors

Yasuyuki Saito, Jana M. Ellegast, Markus G. Manz

Editors

Elodie Segura, Nobuyuki Onai

Abstract

Transplantation of human CD34(+) hematopoietic stem and progenitor cells into severe immunocompromised newborn mice allows the development of a human hemato-lymphoid system (HHLS) including dendritic cells (DCs) in vivo. Therefore, it can be a powerful tool to study human DC subsets, residing in different lymphoid and nonlymphoid organs. We have recently generated novel mouse strains called human cytokine knock-in mice in which human versions of several cytokines are knocked into Rag2(-/-)γC(-/-) strains. In addition, human SIRPα, which is a critical factor to prevent donor cell to be eliminated by host macrophages, is expressed as transgene. These mice efficiently support human myeloid cell development and, indeed, allow the analysis of three major subsets of human DC lineages, plasmacytoid DCs and CD1c(+) and CD141(+) classical DCs. Moreover, these strains also support cytokine-mobilized peripheral blood CD34(+) cell engraftment and subsequent DC development. Here we describe our standard methods to characterize DCs developed in human cytokine knock-in mice.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 9 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 1 11%
Unknown 8 89%

Demographic breakdown

Readers by professional status Count As %
Researcher 2 22%
Other 1 11%
Student > Ph. D. Student 1 11%
Student > Doctoral Student 1 11%
Professor > Associate Professor 1 11%
Other 1 11%
Unknown 2 22%
Readers by discipline Count As %
Immunology and Microbiology 2 22%
Biochemistry, Genetics and Molecular Biology 1 11%
Agricultural and Biological Sciences 1 11%
Medicine and Dentistry 1 11%
Neuroscience 1 11%
Other 1 11%
Unknown 2 22%