Isolation and Characterization of Pluripotent Human Spermatogonial Stem Cell-Derived Cells

Author:

Kossack Nina12,Meneses Juanito3,Shefi Shai45,Nguyen Ha Nam1,Chavez Shawn1,Nicholas Cory1,Gromoll Joerg2,Turek Paul J.4,Reijo-Pera Renee A.1

Affiliation:

1. Institute for Stem Cell Biology and Regenerative Medicine, Department of Obstetrics and Gynecology, Stanford University School of Medicine, Palo Alto, California, USA

2. Center of Reproductive Medicine and Andrology, University of Muenster, Muenster, Germany

3. Center for Reproductive Sciences, University of California, San Francisco, San Francisco, California, USA

4. Department of Urology, University of California, San Francisco, San Francisco, California, USA

5. Sheba Medical Center, Tel Hashomer, Israel

Abstract

Abstract Several reports have documented the derivation of pluripotent cells (multipotent germline stem cells) from spermatogonial stem cells obtained from the adult mouse testis. These spermatogonia-derived stem cells express embryonic stem cell markers and differentiate to the three primary germ layers, as well as the germline. Data indicate that derivation may involve reprogramming of endogenous spermatogonia in culture. Here, we report the derivation of human multipotent germline stem cells (hMGSCs) from a testis biopsy. The cells express distinct markers of pluripotency, form embryoid bodies that contain derivatives of all three germ layers, maintain a normal XY karyotype, are hypomethylated at the H19 locus, and express high levels of telomerase. Teratoma assays indicate the presence of human cells 8 weeks post-transplantation but limited teratoma formation. Thus, these data suggest the potential to derive pluripotent cells from human testis biopsies but indicate a need for novel strategies to optimize hMGSC culture conditions and reprogramming.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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