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Germline Development

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Cover of 'Germline Development'

Table of Contents

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    Book Overview
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    Chapter 1 Isolation of fetal gonads from embryos of timed-pregnant mice for morphological and molecular studies.
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    Chapter 2 Neonatal Testicular Gonocytes Isolation and Processing for Immunocytochemical Analysis
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    Chapter 3 Isolation of Undifferentiated and Early Differentiating Type A Spermatogonia from Pou5f1-GFP Reporter Mice
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    Chapter 4 Isolation of Human Male Germ-Line Stem Cells Using Enzymatic Digestion and Magnetic-Activated Cell Sorting
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    Chapter 5 Isolation and Purification of Murine Male Germ Cells
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    Chapter 6 Preparation of Enriched Mouse Syncitia-Free Pachytene Spermatocyte Cell Suspensions
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    Chapter 7 Revealing the Transcriptome Landscape of Mouse Spermatogonial Cells by Tiling Microarray
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    Chapter 8 Biochemical Characterization of a Testis-Predominant Isoform of N-Alpha Acetyltransferase
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    Chapter 9 Identification of Novel Long Noncoding RNA Transcripts in Male Germ Cells
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    Chapter 10 Methylation Profiling Using Methylated DNA Immunoprecipitation and Tiling Array Hybridization
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    Chapter 11 Spermatogenesis in Cryptorchidism
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    Chapter 12 In Vitro Culture of Fetal Ovaries: A Model to Study Factors Regulating Early Follicular Development
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    Chapter 13 Microspread Ovarian Cell Preparations for the Analysis of Meiotic Prophase Progression in Oocytes with Improved Recovery by Cytospin Centrifugation
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    Chapter 14 In Vitro Maturation (IVM) of Porcine Oocytes
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    Chapter 15 Experimental approaches to the study of human primordial germ cells.
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    Chapter 16 Investigating the Origins of Somatic Cell Populations in the Perinatal Mouse Ovaries Using Genetic Lineage Tracing and Immunohistochemistry
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    Chapter 17 DNA methylation analysis of germ cells by using bisulfite-based sequencing methods.
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    Chapter 18 Gene Expression in Mouse Oocytes by RNA-Seq.
Attention for Chapter 4: Isolation of Human Male Germ-Line Stem Cells Using Enzymatic Digestion and Magnetic-Activated Cell Sorting
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Chapter title
Isolation of Human Male Germ-Line Stem Cells Using Enzymatic Digestion and Magnetic-Activated Cell Sorting
Chapter number 4
Book title
Germline Development
Published in
Methods in molecular biology, January 2012
DOI 10.1007/978-1-61779-436-0_4
Pubmed ID
Book ISBNs
978-1-61779-435-3, 978-1-61779-436-0
Authors

Zuping He, Maria Kokkinaki, Jiji Jiang, Wenxian Zeng, Ina Dobrinski, Martin Dym, He, Zuping, Kokkinaki, Maria, Jiang, Jiji, Zeng, Wenxian, Dobrinski, Ina, Dym, Martin

Abstract

Mammalian spermatogenesis is a process whereby male germ-line stem cells (spermatogonial stem cells) divide and differentiate into sperm. Although a great deal of progress has been made in the isolation and characterization of spermatogonial stem cells (SSCs) in rodents, little is known about human SSCs. We have recently isolated human G protein-coupled receptor 125 (GPR125)-positive spermatogonia and GDNF family receptor alpha 1 (GFRA1)-positive spermatogonia using a 2-step enzymatic digestion and magnetic-activated cell sorting (MACS) from adult human testes. Cell purities of isolated human GPR125- and GFRA1-positive spermatogonia after MACS are greater than 95%, and cell viability is over 96%. The isolated GPR125- and GFRA1-positive spermatogonia coexpress GPR125, integrin, alpha 6 (ITGA6), THY1 (also known as CD90), GFRA1, and ubiquitin carboxyl-terminal esterase L1 (UCHL1), markers for rodent or pig SSCs/progenitors, suggesting that GPR125- and GFRA1-positive spermatogonia are phenotypically the SSCs in human testis. Human GPR125-positive spermatogonia can be cultured for 2 weeks with a remarkable increase in cell number. Immunocytochemistry further reveals that GPR125-positive spermatogonia can be maintained in an undifferentiated state in vitro. Collectively, the methods using enzymatic digestion and MACS can efficiently isolate and purify SSCs from adult human testis with consistent and high quality. The ability of isolating and characterizing human SSCs could provide a population of stem cells with high purity for mechanistic studies on human SSC self-renewal and differentiation as well as potential applications of human SSCs in regenerative medicine.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 27 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 27 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 6 22%
Student > Master 4 15%
Professor 3 11%
Student > Ph. D. Student 3 11%
Student > Doctoral Student 1 4%
Other 4 15%
Unknown 6 22%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 7 26%
Agricultural and Biological Sciences 4 15%
Medicine and Dentistry 4 15%
Engineering 2 7%
Immunology and Microbiology 1 4%
Other 2 7%
Unknown 7 26%