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Stress Responses

Overview of attention for book
Stress Responses
Springer New York

Table of Contents

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    Book Overview
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    Chapter 1 Methods for Studying ER Stress and UPR Markers in Human Cells
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    Chapter 2 Assays for Induction of the Unfolded Protein Response and Selective Activation of the Three Major Pathways
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    Chapter 3 Assays to Characterize Molecular Chaperone Function In Vitro
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    Chapter 4 Analysis of the Heat Shock Factor Complex in Mammalian HSP70 Promoter.
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    Chapter 5 Immunofluorescence-Based Methods to Monitor DNA End Resection
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    Chapter 6 Visualizing the spatiotemporal dynamics of DNA damage in budding yeast.
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    Chapter 7 Detecting reactive oxygen species by immunohistochemistry.
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    Chapter 8 Investigating Inflammasome Activation Under Conditions of Cellular Stress and Injury
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    Chapter 9 Methods for Studying microRNA Functions During Stress.
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    Chapter 10 Measuring autophagy in stressed cells.
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    Chapter 11 Detection of Apoptosis Using Fluorescent Probes
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    Chapter 12 Measuring Death of Pancreatic Beta Cells in Response to Stress and Cytotoxic T Cells
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    Chapter 13 Adaptation of the Secretory Pathway in Cancer Through IRE1 Signaling
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    Chapter 14 Studying nitrosative stress in Parkinson's disease.
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    Chapter 15 Cross Talk Between ER Stress, Oxidative Stress, and Inflammation in Health and Disease
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    Chapter 16 Stress Responses During Ageing: Molecular Pathways Regulating Protein Homeostasis
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    Chapter 17 Targeting Stress Responses for Regenerative Medicine
Attention for Chapter 12: Measuring Death of Pancreatic Beta Cells in Response to Stress and Cytotoxic T Cells
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Chapter title
Measuring Death of Pancreatic Beta Cells in Response to Stress and Cytotoxic T Cells
Chapter number 12
Book title
Stress Responses
Published in
Methods in molecular biology, March 2015
DOI 10.1007/978-1-4939-2522-3_12
Pubmed ID
Book ISBNs
978-1-4939-2521-6, 978-1-4939-2522-3
Authors

Wali, Jibran A., Trivedi, Prerak, Kay, Thomas W., Thomas, Helen E., Jibran A. Wali, Prerak Trivedi, Thomas W. Kay, Helen E. Thomas

Abstract

Apoptosis of pancreatic beta cells is a feature of type 1 and type 2 diabetes, although by different effector mechanisms. In type 1 diabetes, beta cells are the targets of cytotoxic CD8(+) T cells that kill by releasing the contents of their cytotoxic granules into the immunological synapse with the target beta cell. In type 2 diabetes, the mechanisms of beta cell apoptosis are less clear, but believed to be due to cellular stresses including endoplasmic reticulum stress and oxidative stress induced by chronic exposure to high concentrations of glucose, lipids, inflammatory cytokines, or islet amyloid polypeptide. Measuring apoptosis in primary islets can be more difficult than in a beta cell line because islets exist as a cluster of cells and it is often difficult to obtain sufficient cells for any particular type of assay. Here, we describe two different methods for measuring islet cell apoptosis. The first method is the measurement of DNA fragmentation, a hallmark of apoptosis, of islets that have been cultured with reagents that induce stress. The second method is the measurement of islet lysis by activated cytotoxic T cells. We describe methods using mouse islets, but these can easily be adapted for human islets.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 19 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 19 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 6 32%
Researcher 5 26%
Student > Doctoral Student 1 5%
Unspecified 1 5%
Student > Master 1 5%
Other 1 5%
Unknown 4 21%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 5 26%
Medicine and Dentistry 4 21%
Agricultural and Biological Sciences 2 11%
Unspecified 1 5%
Chemistry 1 5%
Other 2 11%
Unknown 4 21%