↓ Skip to main content

Cellular Quiescence

Overview of attention for book
Cover of 'Cellular Quiescence'

Table of Contents

  1. Altmetric Badge
    Book Overview
  2. Altmetric Badge
    Chapter 1 Molecular Regulation of Cellular Quiescence: A Perspective from Adult Stem Cells and Its Niches
  3. Altmetric Badge
    Chapter 2 An In Vitro Model of Cellular Quiescence in Primary Human Dermal Fibroblasts
  4. Altmetric Badge
    Chapter 3 Flow Cytometric Detection of G0 in Live Cells by Hoechst 33342 and Pyronin Y Staining
  5. Altmetric Badge
    Chapter 4 Using Carboxy Fluorescein Succinimidyl Ester (CFSE) to Identify Quiescent Glioblastoma Stem-Like Cells
  6. Altmetric Badge
    Chapter 5 Isolation of Neural Stem and Progenitor Cells from the Adult Brain and Live Imaging of Their Cell Cycle with the FUCCI System
  7. Altmetric Badge
    Chapter 6 Determination of Histone 2B–Green Fluorescent Protein (GFP) Retention in Intestinal Stem Cells
  8. Altmetric Badge
    Chapter 7 Detecting Hematopoietic Stem Cell Proliferation Using BrdU Incorporation
  9. Altmetric Badge
    Chapter 8 Cell Cycle Analysis by Mass Cytometry
  10. Altmetric Badge
    Chapter 9 Preparation and Analysis of Saccharomyces cerevisiae Quiescent Cells
  11. Altmetric Badge
    Chapter 10 Identifying Quiescent Stem Cells in Hair Follicles
  12. Altmetric Badge
    Chapter 11 Single EDL Myofiber Isolation for Analyses of Quiescent and Activated Muscle Stem Cells
  13. Altmetric Badge
    Chapter 12 Investigating Cellular Quiescence of T Lymphocytes and Antigen-Induced Exit from Quiescence
  14. Altmetric Badge
    Chapter 13 Retroviral Transduction of Quiescent Murine Hematopoietic Stem Cells
  15. Altmetric Badge
    Chapter 14 Analysis of Murine Hematopoietic Stem Cell Proliferation During Inflammation
  16. Altmetric Badge
    Chapter 15 A Facile, In Vitro 384-Well Plate System to Model Disseminated Tumor Cells in the Bone Marrow Microenvironment
  17. Altmetric Badge
    Chapter 16 Distinguishing States of Arrest: Genome-Wide Descriptions of Cellular Quiescence Using ChIP-Seq and RNA-Seq Analysis
  18. Altmetric Badge
    Chapter 17 Analysis of lncRNA-Protein Interactions by RNA-Protein Pull-Down Assays and RNA Immunoprecipitation (RIP)
  19. Altmetric Badge
    Chapter 18 Analysis of MicroRNA-Mediated Translation Activation of In Vitro Transcribed Reporters in Quiescent Cells
  20. Altmetric Badge
    Chapter 19 Genome-Wide Identification of Transcription Factor-Binding Sites in Quiescent Adult Neural Stem Cells
  21. Altmetric Badge
    Chapter 20 Study Quiescence Heterogeneity by Coupling Single-Cell Measurements and Computer Modeling
Attention for Chapter 10: Identifying Quiescent Stem Cells in Hair Follicles
Altmetric Badge

Citations

dimensions_citation
4 Dimensions

Readers on

mendeley
7 Mendeley
You are seeing a free-to-access but limited selection of the activity Altmetric has collected about this research output. Click here to find out more.
Chapter title
Identifying Quiescent Stem Cells in Hair Follicles
Chapter number 10
Book title
Cellular Quiescence
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-7371-2_10
Pubmed ID
Book ISBNs
978-1-4939-7370-5, 978-1-4939-7371-2
Authors

Christine N. Rodriguez, Hoang Nguyen

Abstract

Hair follicle stem cells (HFSCs) are noted for their relative quiescence and therefore can be distinguished from other cells by their differential history of cell division. Replicating cells can be labeled by pulsing the animals repeatedly with 5-bromo-2'-deoxyuridine (BrdU) or tritiated thymidine ([(3)H]TdR), thymidine analogs that get incorporated into DNA during DNA synthesis. Because dividing cells dilute the label after each cell division, frequently dividing cells will lose the label over time while slow cycling cells will retain the label and thus are termed label retaining cells (LRCs). [(3)H]TdR can be visualized by autoradiography and BrdU can be detected by immunofluorescence with anti-BrdU antibodies. Alternatively, a well-established tet-regulatable transgenic mouse model can be used to express histone H2B-GFP in epithelial proliferative cells and their dilution and retention of the GFP signal can be followed. In this chapter, we detail the steps to perform BrdU pulse-chase and H2B-GFP pulse-chase experiments to identify quiescent cells in the hair follicle.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 7 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 7 100%

Demographic breakdown

Readers by professional status Count As %
Lecturer 1 14%
Student > Doctoral Student 1 14%
Student > Bachelor 1 14%
Student > Master 1 14%
Researcher 1 14%
Other 0 0%
Unknown 2 29%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 2 29%
Medicine and Dentistry 2 29%
Neuroscience 1 14%
Design 1 14%
Unknown 1 14%