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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 10: Differentiation-Promoting Medium Additives for Hepatocyte Cultivation and Cryopreservation
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Chapter title
Differentiation-Promoting Medium Additives for Hepatocyte Cultivation and Cryopreservation
Chapter number 10
Book title
Protocols in In Vitro Hepatocyte Research
Published in
Methods in molecular biology, January 2015
DOI 10.1007/978-1-4939-2074-7_10
Pubmed ID
Book ISBNs
978-1-4939-2073-0, 978-1-4939-2074-7
Authors

Varvara Gouliarmou, Olavi Pelkonen, Sandra Coecke, Gouliarmou, Varvara, Pelkonen, Olavi, Coecke, Sandra

Abstract

Isolated primary hepatocytes are considered as the reference system for in vitro hepatic methods. Following the isolation of primary hepatocytes from liver tissue, an unfavorable process named dedifferentiation is initiated leading to the attenuation of the hepatocellular phenotype both at the morphological and functional level. Freshly isolated hepatocytes can be used immediately or can be cryopreserved for future purposes. Currently, a number of antidedifferentiation strategies exist to extend the life span of isolated hepatocytes. The addition of differentiation-promoting compounds to the hepatocyte culture medium is the oldest and simplest antidedifferentiation approach applied. In the present chapter, the most commonly used medium additives for cultivation and cryopreservation of primary hepatocytes are reviewed.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 15 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 15 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 4 27%
Student > Ph. D. Student 3 20%
Professor 1 7%
Other 1 7%
Student > Master 1 7%
Other 1 7%
Unknown 4 27%
Readers by discipline Count As %
Pharmacology, Toxicology and Pharmaceutical Science 4 27%
Agricultural and Biological Sciences 3 20%
Nursing and Health Professions 1 7%
Social Sciences 1 7%
Engineering 1 7%
Other 0 0%
Unknown 5 33%