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Oral Biology

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Cover of 'Oral Biology'

Table of Contents

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    Book Overview
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    Chapter 1 Salivary Diagnostics Using Purified Nucleic Acids
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    Chapter 2 RNA Sequencing Analysis of Salivary Extracellular RNA
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    Chapter 3 Qualitative and Quantitative Proteome Analysis of Oral Fluids in Health and Periodontal Disease by Mass Spectrometry
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    Chapter 4 Antioxidant Micronutrients and Oxidative Stress Biomarkers
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    Chapter 5 NMR-Based Metabolomics of Oral Biofluids
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    Chapter 6 Gene Therapy of Salivary Diseases
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    Chapter 7 The Oral Microbiota in Health and Disease: An Overview of Molecular Findings
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    Chapter 8 Microbial Community Profiling Using Terminal Restriction Fragment Length Polymorphism (T-RFLP) and Denaturing Gradient Gel Electrophoresis (DGGE)
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    Chapter 9 Analysis of 16S rRNA Gene Amplicon Sequences Using the QIIME Software Package
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    Chapter 10 Adhesion of Yeast and Bacteria to Oral Surfaces
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    Chapter 11 Quantitative Analysis of Periodontal Pathogens Using Real-Time Polymerase Chain Reaction (PCR)
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    Chapter 12 Methods to Study Antagonistic Activities Among Oral Bacteria
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    Chapter 13 Natural Transformation of Oral Streptococci by Use of Synthetic Pheromones
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    Chapter 14 Markerless Genome Editing in Competent Streptococci
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    Chapter 15 Tools and Strategies for Analysis of Genome-Wide and Gene-Specific DNA Methylation Patterns
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    Chapter 16 Generating Multiple Base-Resolution DNA Methylomes Using Reduced Representation Bisulfite Sequencing
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    Chapter 17 A Protocol for the Determination of the Methylation Status of Gingival Tissue DNA at Specific CpG Islands
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    Chapter 18 Genome-Wide Analysis of Periodontal and Peri-Implant Cells and Tissues
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    Chapter 19 Differential Expression and Functional Analysis of High-Throughput -Omics Data Using Open Source Tools
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    Chapter 20 Exploring Genome-Wide Expression Profiles Using Machine Learning Techniques
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    Chapter 21 Embryonic Explant Culture: Studying Effects of Regulatory Molecules on Gene Expression in Craniofacial Tissues
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    Chapter 22 Oral Epithelial Cell Culture Model for Studying the Pathogenesis of Chronic Inflammatory Disease
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    Chapter 23 Fabrication and Characterization of Decellularized Periodontal Ligament Cell Sheet Constructs
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    Chapter 24 A Method to Isolate, Purify, and Characterize Human Periodontal Ligament Stem Cells
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    Chapter 25 Constructing Tissue Microarrays: Protocols and Methods Considering Potential Advantages and Disadvantages for Downstream Use
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    Chapter 26 Growing Adipose-Derived Stem Cells Under Serum-Free Conditions
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    Chapter 27 Quantitative Real-Time Gene Profiling of Human Alveolar Osteoblasts
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    Chapter 28 Proteomic Analysis of Dental Tissue Microsamples
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    Chapter 29 Characterization, Quantification, and Visualization of Neutrophil Extracellular Traps
Attention for Chapter 24: A Method to Isolate, Purify, and Characterize Human Periodontal Ligament Stem Cells
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Chapter title
A Method to Isolate, Purify, and Characterize Human Periodontal Ligament Stem Cells
Chapter number 24
Book title
Oral Biology
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6685-1_24
Pubmed ID
Book ISBNs
978-1-4939-6683-7, 978-1-4939-6685-1
Authors

Krzysztof Mrozik, Stan Gronthos, Songtao Shi, P. Mark Bartold, Mrozik, Krzysztof, Gronthos, Stan, Shi, Songtao, Bartold, P. Mark

Editors

Gregory J. Seymour, Mary P. Cullinan, Nicholas C.K. Heng

Abstract

Human periodontal ligament stem cells (PDLSCs) are a unique population of mesenchymal stem cells (MSCs) that demonstrate the capacity to generate cementum- and periodontal ligament-like structures in vivo. As such, PDLSCs represent a promising cell-based therapy in reconstructive dentistry for the treatment of periodontal disease. The present chapter describes two methods for isolating PDLSCs from human PDL tissue including traditional plastic adherence, and immunomagnetic selection based on the expression of MSC-associated surface markers STRO-1 antigen, CD146 (MUC-18), CD29 (Integrin β-1), CD44, and CD106 (VCAM-1). Although no single antibody demonstrates specificity for MSCs, isolation based on expression of individual markers results in homogenous preparations of PDLSCs. Methods to further characterize the immunophenotype and multipotent capacity of PDLSCs to differentiate into adipocytes, osteoblast-, and cementoblast-like cells in vitro, and cementum- and periodontal ligament-like tissues in vivo, are also described.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 29 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 29 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 5 17%
Student > Ph. D. Student 4 14%
Student > Bachelor 3 10%
Student > Doctoral Student 2 7%
Student > Postgraduate 2 7%
Other 5 17%
Unknown 8 28%
Readers by discipline Count As %
Medicine and Dentistry 12 41%
Biochemistry, Genetics and Molecular Biology 4 14%
Materials Science 1 3%
Psychology 1 3%
Unknown 11 38%