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Sertoli Cells

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Cover of 'Sertoli Cells'

Table of Contents

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    Book Overview
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    Chapter 1 Establishment of Primary Culture of Sertoli Cells
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    Chapter 2 Evaluation of the Purity of Sertoli Cell Primary Cultures
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    Chapter 3 Preparation of Testicular Samples for Histology and Immunohistochemistry
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    Chapter 4 Rabbit Sertoli Cells: Immunohistochemical Profile from Neonatal to Adult Age
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    Chapter 5 Identification of Proliferative and Apoptotic Sertoli Cells Using Fluorescence and Confocal Microscopy
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    Chapter 6 Sertoli Cell Preparation for Co-immunoprecipitation
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    Chapter 7 Profiling Signaling Proteins in Sertoli Cells by Co-immunoprecipitation
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    Chapter 8 Phagocytosis by Sertoli Cells: Analysis of Main Phagocytosis Steps by Confocal and Electron Microscopy
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    Chapter 9 A Method for In Vivo Induction and Ultrastructural Detection of Mitophagy in Sertoli Cells
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    Chapter 10 Assessing Autophagy in Sertoli Cells
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    Chapter 11 Molecular Mechanisms and Signaling Pathways Involved in the Nutritional Support of Spermatogenesis by Sertoli Cells
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    Chapter 12 Assessing Sertoli Cell Metabolic Activity
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    Chapter 13 Proteome Profiling of Sertoli Cells Using a GeLC-MS/MS Strategy
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    Chapter 14 Gene Silencing of Human Sertoli Cells Utilizing Small Interfering RNAs
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    Chapter 15 Testicular Cell Selective Ablation Using Diphtheria Toxin Receptor Transgenic Mice
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    Chapter 16 Regulation of Blood-Testis Barrier (BTB) Dynamics, Role of Actin-, and Microtubule-Based Cytoskeletons
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    Chapter 17 Monitoring the Integrity of the Blood-Testis Barrier (BTB): An In Vivo Assay
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    Chapter 18 Computational Methods Involved in Evaluating the Toxicity of the Reproductive Toxicants in Sertoli Cell
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    Chapter 19 A Stopped-Flow Light Scattering Methodology for Assessing the Osmotic Water Permeability of Whole Sertoli Cells
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    Chapter 20 Cryopreservation of Human Testicular Tissue by Isopropyl-Controlled Slow Freezing
Attention for Chapter 5: Identification of Proliferative and Apoptotic Sertoli Cells Using Fluorescence and Confocal Microscopy
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Chapter title
Identification of Proliferative and Apoptotic Sertoli Cells Using Fluorescence and Confocal Microscopy
Chapter number 5
Book title
Sertoli Cells
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-7698-0_5
Pubmed ID
Book ISBNs
978-1-4939-7697-3, 978-1-4939-7698-0
Authors

Jesús Martínez-Hernández, Vicente Seco-Rovira, Ester Beltrán-Frutos, Victor Quesada-Cubo, Concepción Ferrer, Luis Miguel Pastor, Martínez-Hernández, Jesús, Seco-Rovira, Vicente, Beltrán-Frutos, Ester, Quesada-Cubo, Victor, Ferrer, Concepción, Pastor, Luis Miguel

Abstract

Sertoli cells, the testicular somatic cells of the seminiferous epithelium, are vital for the survival of the epithelium. They undergo proliferation and apoptosis during fetal, neonatal, and prepubertal development. Apoptosis is increased in certain situations such as exposure to many substances, for example, toxics, or short photoperiod in the non-breeding season of some mammals. Therefore, it has always been considered that Sertoli cells that reach adulthood are quiescent cells, that is to say, nonproliferative, do not die, are terminally differentiated, and whose numbers remain constant. Recently, a degree of both proliferation and apoptosis has been observed in normal adult conditions, suggesting that consideration of this cell as quiescent may be subject to change. All this make it necessary to use histochemical techniques to demonstrate whether Sertoli cells are undergoing proliferation or apoptosis in histological sections and to allow the qualitative and quantitative study of these. In this chapter, we present two double-staining techniques that can be used for identifying Sertoli cells in proliferation or apoptosis by fluorescence microscopy. In both, the Sertoli cells are identified by an immunohistochemistry for vimentin followed by an immunohistochemistry for PCNA or a TUNEL histochemistry.

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Mendeley readers

The data shown below were compiled from readership statistics for 2 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 2 100%

Demographic breakdown

Readers by professional status Count As %
Professor 1 50%
Researcher 1 50%
Readers by discipline Count As %
Immunology and Microbiology 1 50%
Unknown 1 50%