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Inflammation

Overview of attention for book
Cover of 'Inflammation'

Table of Contents

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    Book Overview
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    Chapter 1 Reproducibility Issues: Avoiding Pitfalls in Animal Inflammation Models
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    Chapter 2 Hapten-Specific T Cell-Mediated Skin Inflammation: Flow Cytometry Analysis of Mouse Skin Inflammatory Infiltrate
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    Chapter 3 Monitoring Skin Dendritic Cells in Steady State and Inflammation by Immunofluorescence Microscopy and Flow Cytometry
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    Chapter 4 Visualization of the T Cell Response in Contact Hypersensitivity
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    Chapter 5 Ultraviolet Radiation-Induced Immunosuppression: Induction of Regulatory T Cells
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    Chapter 6 Surgical Denervation in the Imiquimod-Induced Psoriasiform Mouse Model
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    Chapter 7 Xenotransplantation Model of Psoriasis
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    Chapter 8 A Mouse Model for Atopic Dermatitis Using Topical Application of Vitamin D3 or of Its Analog MC903
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    Chapter 9 Particle Bombardment of Ex Vivo Skin to Deliver DNA and Express Proteins
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    Chapter 10 Murine Models of Allergic Asthma
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    Chapter 11 Subcutaneous and Sublingual Immunotherapy in a Mouse Model of Allergic Asthma
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    Chapter 12 Characterization of Group 2 Innate Lymphoid Cells in Allergic Airway Inflammation Models in the Mouse
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    Chapter 13 Induction and Analysis of Bronchus-Associated Lymphoid Tissue
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    Chapter 14 Messenger RNA Sequencing of Rare Cell Populations in the Lung and Lung-Draining Lymph Nodes
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    Chapter 15 Isolation and Identification of Intestinal Myeloid Cells
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    Chapter 16 Monitoring and Modulation of Inducible Foxp3+ Regulatory T-Cell Differentiation in the Lymph Nodes Draining the Small Intestine and Colon
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    Chapter 17 Isolation and Flow Cytometry Analysis of Innate Lymphoid Cells from the Intestinal Lamina Propria
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    Chapter 18 Analysis of Leukocytes in Oral Mucosal Tissues
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    Chapter 19 Optimized Mouse Models for Liver Fibrosis
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    Chapter 20 Monitoring of Chemically Induced Colitis
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    Chapter 21 Oxazolone-Induced Intestinal Inflammation in Adult Zebrafish
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    Chapter 22 High Dimensional Cytometry of Central Nervous System Leukocytes During Neuroinflammation
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    Chapter 23 Isolation of Microglia and Immune Infiltrates from Mouse and Primate Central Nervous System
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    Chapter 24 Investigating the Lymphatic Drainage of the Brain: Essential Skills and Tools
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    Chapter 25 Quantitative Assessment of Cerebral Basement Membranes Using Electron Microscopy
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    Chapter 26 Microglial Activation by Genetically Targeted Conditional Neuronal Ablation in the Zebrafish
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    Chapter 27 Experimental Arthritis Mouse Models Driven by Adaptive and/or Innate Inflammation
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    Chapter 28 Pain Relief in Nonhuman Primate Models of Arthritis
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    Chapter 29 Isolation and Characterization of Aortic Dendritic Cells and Lymphocytes in Atherosclerosis
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    Chapter 30 Assessment of Vascular Dysfunction and Inflammation Induced by Angiotensin II in Mice
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    Chapter 31 Erratum to: Isolation and Characterization of Aortic Dendritic Cells and Lymphocytes in Atherosclerosis
Attention for Chapter 23: Isolation of Microglia and Immune Infiltrates from Mouse and Primate Central Nervous System
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Chapter title
Isolation of Microglia and Immune Infiltrates from Mouse and Primate Central Nervous System
Chapter number 23
Book title
Inflammation
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6786-5_23
Pubmed ID
Book ISBNs
978-1-4939-6784-1, 978-1-4939-6786-5
Authors

Thais F. Galatro, Ilia D. Vainchtein, Nieske Brouwer, Erik W. G. M. Boddeke, Bart J. L. Eggen

Editors

Björn E. Clausen, Jon D. Laman

Abstract

Microglia are the innate immune cells of the central nervous system (CNS) and play an important role in the maintenance of tissue homeostasis, providing neural support and neuroprotection. Microglia constantly survey their environment and quickly respond to homeostatic perturbations. Microglia are increasingly implicated in neuropathological and neurodegenerative conditions, such as Alzheimer's disease, Parkinson's disease, and glioma progression. Here, we describe a detailed isolation protocol for microglia and immune infiltrates, optimized for large amounts of post mortem tissue from human and rhesus macaque, as well as smaller tissue amounts from mouse brain and spinal cord, that yield a highly purified microglia population (up to 98 % purity). This acute isolation protocol is based on mechanical dissociation and a two-step density gradient purification, followed by fluorescence-activated cell sorting (FACS) to obtain pure microglia and immune infiltrate populations.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 77 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 77 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 24 31%
Student > Master 11 14%
Student > Bachelor 8 10%
Researcher 8 10%
Student > Doctoral Student 6 8%
Other 12 16%
Unknown 8 10%
Readers by discipline Count As %
Neuroscience 32 42%
Biochemistry, Genetics and Molecular Biology 12 16%
Medicine and Dentistry 9 12%
Agricultural and Biological Sciences 7 9%
Immunology and Microbiology 2 3%
Other 6 8%
Unknown 9 12%