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Protocols in In Vitro Hepatocyte Research

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Cover of 'Protocols in In Vitro Hepatocyte Research'

Table of Contents

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    Book Overview
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    Chapter 1 Isolation and Culture of Mouse Hepatocytes: Gender-Specific Gene Expression Responses to Chemical Treatments
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    Chapter 2 Cryopreservation of Hepatocytes
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    Chapter 3 Protocols in In Vitro Hepatocyte Research
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    Chapter 4 Immortalized Human Hepatic Cell Lines for In Vitro Testing and Research Purposes
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    Chapter 5 Culture and Functional Characterization of Human Hepatoma HepG2 Cells
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    Chapter 6 Establishment and Characterization of an In Vitro Model of Fas-Mediated Hepatocyte Cell Death
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    Chapter 7 Serum-Free Directed Differentiation of Human Embryonic Stem Cells to Hepatocytes
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    Chapter 8 Human Skin-Derived Precursor Cells: Isolation, Expansion, and Hepatic Differentiation
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    Chapter 9 Generation of Hepatocytes from Pluripotent Stem Cells for Drug Screening and Developmental Modeling.
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    Chapter 10 Differentiation-Promoting Medium Additives for Hepatocyte Cultivation and Cryopreservation
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    Chapter 11 Coculture and Long-Term Maintenance of Hepatocytes.
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    Chapter 12 Primary Hepatocytes in Sandwich Culture
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    Chapter 13 Establishing Liver Bioreactors for In Vitro Research
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    Chapter 14 Epigenetic Modifications as Antidedifferentiation Strategy for Primary Hepatocytes in Culture.
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    Chapter 15 Transfection of Primary Hepatocytes with Liver-Enriched Transcription Factors Using Adenoviral Vectors
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    Chapter 16 Transcriptomics of Hepatocytes Treated with Toxicants for Investigating Molecular Mechanisms Underlying Hepatotoxicity.
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    Chapter 17 Global MicroRNA Analysis in Primary Hepatocyte Cultures.
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    Chapter 18 Mass Spectrometry-Based Proteomics for Relative Protein Quantification and Biomarker Identification in Primary Human Hepatocytes
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    Chapter 19 Targeted Metabolomics for Homocysteine-Related Metabolites in Primary Hepatocytes
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    Chapter 20 Measurement of Cytochrome P450 Enzyme Induction and Inhibition in Human Hepatoma Cells
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    Chapter 21 Analysis of Sinusoidal Drug Uptake Transporter Activities in Primary Human Hepatocytes
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    Chapter 22 Measurement of Albumin Secretion as Functionality Test in Primary Hepatocyte Cultures
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    Chapter 23 Measurement of Blood Coagulation Factor Synthesis in Cultures of Human Hepatocytes
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    Chapter 24 Functionality Testing of Primary Hepatocytes in Culture by Measuring Urea Synthesis
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    Chapter 25 Protocols in In Vitro Hepatocyte Research
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    Chapter 26 General Cytotoxicity Assessment by Means of the MTT Assay
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    Chapter 27 Measurement of Apoptotic and Necrotic Cell Death in Primary Hepatocyte Cultures
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    Chapter 28 Critical Factors in the Assessment of Cholestatic Liver Injury In Vitro
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    Chapter 29 In Vitro Cell Culture Models of Hepatic Steatosis
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    Chapter 30 Assessment of Liver Fibrotic Insults In Vitro
Attention for Chapter 27: Measurement of Apoptotic and Necrotic Cell Death in Primary Hepatocyte Cultures
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Chapter title
Measurement of Apoptotic and Necrotic Cell Death in Primary Hepatocyte Cultures
Chapter number 27
Book title
Protocols in In Vitro Hepatocyte Research
Published in
Methods in molecular biology, January 2015
DOI 10.1007/978-1-4939-2074-7_27
Pubmed ID
Book ISBNs
978-1-4939-2073-0, 978-1-4939-2074-7
Authors

Michaël Maes, Tamara Vanhaecke, Bruno Cogliati, Sara Crespo Yanguas, Joost Willebrords, Vera Rogiers, Mathieu Vinken, Maes, Michaël, Vanhaecke, Tamara, Cogliati, Bruno, Yanguas, Sara Crespo, Willebrords, Joost, Rogiers, Vera, Vinken, Mathieu

Abstract

Hepatotoxicity, including drug-induced liver injury, is frequently accompanied by cell death. The latter is typically driven by apoptosis or necrosis, which substantially differ based upon biochemical and morphological criteria. This chapter describes two commonly used methods to probe apoptotic and necrotic activities in adherent monolayer cultures of primary hepatocytes. The apoptosis assay uses a prototypical substrate of caspase 3, the main executor of apoptotic cell death, which can be cleaved, yielding a product that can be measured fluorimetrically. The second assay relies on the disruption of the cell plasma membrane, which typically occurs in necrotic cell death and that results in the extracellular release of cytoplasmic enzymes, such as lactate dehydrogenase. The latter can be indirectly assessed by spectrophotometrically measuring the consumption of reduced nicotinamide adenine dinucleotide.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 71 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 71 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 12 17%
Student > Ph. D. Student 9 13%
Researcher 9 13%
Student > Master 9 13%
Student > Doctoral Student 5 7%
Other 5 7%
Unknown 22 31%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 10 14%
Pharmacology, Toxicology and Pharmaceutical Science 9 13%
Agricultural and Biological Sciences 6 8%
Medicine and Dentistry 6 8%
Veterinary Science and Veterinary Medicine 4 6%
Other 11 15%
Unknown 25 35%