iPSCs derived from infertile men carrying complex genetic abnormalities can generate primordial germ-like cells

Author:

Mouka Aurélie,Arkoun Brahim,Moison Pauline,Drévillon Loïc,Jarray Rafika,Brisset Sophie,Mayeur Anne,Bouligand Jérôme,Boland-Auge Anne,Deleuze Jean-François,Yates Frank,Lemonnier Thomas,Callier Patrick,Duffourd Yannis,Nitschke Patrick,Ollivier Emmanuelle,Bourdin Arnaud,De Vos John,Livera Gabriel,Tachdjian Gérard,Maouche-Chrétien LeïlaORCID,Tosca Lucie

Abstract

AbstractDespite increasing insight into the genetics of infertility, the developmental disease processes remain unclear due to the lack of adequate experimental models. The advent of induced pluripotent stem cell (iPSC) technology has provided a unique tool for in vitro disease modeling enabling major advances in our understanding of developmental disease processes. We report the full characterization of complex genetic abnormalities in two infertile patients with either azoospermia or XX male syndrome and we identify genes of potential interest implicated in their infertility. Using the erythroblasts of both patients, we generated primed iPSCs and converted them into a naive-like pluripotent state. Naive-iPSCs were then differentiated into primordial germ-like cells (PGC-LCs). The expression of early PGC marker genes SOX17CD-38, NANOS3, c-KITTFAP2C, and D2-40, confirmed progression towards the early germline stage. Our results demonstrate that iPSCs from two infertile patients with significant genetic abnormalities are capable of efficient production of PGCs. Such in vitro model of infertility will certainly help identifying causative factors leading to early germ cells development failure and provide a valuable tool to explore novel therapeutic strategies.

Funder

French Ministry

Institut Universitaire de France and DIM region Ile de France

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

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