Modeling mammalian spermatogonial differentiation and meiotic initiation in vitro

Author:

Kirsanov Oleksandr1,Johnson Taylor1,Malachowski Taylor1,Niedenberger Bryan A.1,Gilbert Emma A.1,Bhowmick Debajit2,Ozdinler P. Hande3,Gray Douglas A.45,Fisher-Wellman Kelsey67,Hermann Brian P.8,Geyer Christopher B.17ORCID

Affiliation:

1. Brody School of Medicine, East Carolina University 1 Department of Anatomy and Cell Biology , , Greenville, NC 27834 , USA

2. Brody School of Medicine, East Carolina University 2 Flow Cytometry Facility , , Greenville, NC 27834 , USA

3. Feinberg School of Medicine, Northwestern University 3 Department of Neurology , , Evanston, IL 60611 , USA

4. University of Ottawa 4 Department of Biochemistry, Microbiology, and Immunology , , Ottawa, K1H 8M5 , Canada

5. Cancer Therapeutics, Ottawa Hospital Research Institute 5 , Ottawa, K1H 8L6 , Canada

6. Brody School of Medicine, East Carolina University 6 Department of Physiology , , Greenville, NC 27858 , USA

7. East Carolina Diabetes and Obesity Institute, East Carolina University 7 , Greenville, NC 27858 , USA

8. University of Texas at San Antonio 8 Department of Neuroscience, Developmental and Regenerative Biology , , San Antonio, TX 78249 , USA

Abstract

ABSTRACT In mammalian testes, premeiotic spermatogonia respond to retinoic acid by completing an essential lengthy differentiation program before initiating meiosis. The molecular and cellular changes directing these developmental processes remain largely undefined. This wide gap in knowledge is due to two unresolved technical challenges: (1) lack of robust and reliable in vitro models to study differentiation and meiotic initiation; and (2) lack of methods to isolate large and pure populations of male germ cells at each stage of differentiation and at meiotic initiation. Here, we report a facile in vitro differentiation and meiotic initiation system that can be readily manipulated, including the use of chemical agents that cannot be safely administered to live animals. In addition, we present a transgenic mouse model enabling fluorescence-activated cell sorting-based isolation of millions of spermatogonia at specific developmental stages as well as meiotic spermatocytes.

Funder

National Institutes of Health

Male Contraceptive Initiative

East Carolina University

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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