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Rheumatoid Arthritis

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Cover of 'Rheumatoid Arthritis'

Table of Contents

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    Book Overview
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    Chapter 1 Collagen-Induced Arthritis Models
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    Chapter 2 Human Xenograft Model
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    Chapter 3 Long-Term Constant Subcutaneous Drug Administration
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    Chapter 4 Clinical Scoring of Disease Activity in Animal Models
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    Chapter 5 Histological Analysis of Arthritic Joints
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    Chapter 6 Preparation of Joint Extracts
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    Chapter 7 Production of Immunizing Antigen Proteoliposome Using Cell-Free Protein Synthesis System
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    Chapter 8 Reconstruction of Protein/Liposome Complex
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    Chapter 9 Production of Neutralizing Antibody
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    Chapter 10 Autoantibody Profiling Using Human Autoantigen Protein Array and AlphaScreen
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    Chapter 11 Generation of Specific Aptamers
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    Chapter 12 Production of Lentiviral Particles
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    Chapter 13 RNA Interference Ex Vivo
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    Chapter 14 Lentiviral-Mediated Systemic RNA Interference In Vivo
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    Chapter 15 Mesenchymal Stem Cell Engineering
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    Chapter 16 Screening of Ca2+ Influx in Lymphocytes
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    Chapter 17 Single-Cell Ca2+ Imaging
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    Chapter 18 Electrophysiological Methods to Measure Ca2+ Current
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    Chapter 19 The Functional Assessment of T cells
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    Chapter 20 Release of Antibodies and Cytokines from B Cells
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    Chapter 21 Evaluation of Autoreactive Responses
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    Chapter 22 Bone Resorption Activity in Mature Osteoclasts
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    Chapter 23 Animal Models of Vasculitis
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    Chapter 24 Design an Intervention Study
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    Chapter 25 Assessment of Disease Activity, Structural Damage, and Function in Rheumatoid Arthritis
Attention for Chapter 18: Electrophysiological Methods to Measure Ca2+ Current
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Chapter title
Electrophysiological Methods to Measure Ca2+ Current
Chapter number 18
Book title
Rheumatoid Arthritis
Published in
Methods in molecular biology, September 2018
DOI 10.1007/978-1-4939-8802-0_18
Pubmed ID
Book ISBNs
978-1-4939-8801-3, 978-1-4939-8802-0
Authors

Shuang Liu, Miyuki Kuno

Abstract

To achieve the most accurate assessment of functional Ca2+ channel or modulator properties and their regulation, a patch clamp technique to record membrane currents is required. This technique has wide applications ranging from recording the activity of native channels in their natural environment to that of recombinant channels expressed in heterologous cells. This chapter introduces the methods that have been used for the detection of calcium release-activated calcium (CRAC) currents, one of the store-operated calcium entry pathways, in human primary T cells. This standard protocol is for laboratories already equipped with a full patch clamp setup or for investigators collaborating with laboratories experienced in patch clamp.