The most severe form of male infertility is characterised by the absence of germ cells from the seminiferous tubules (Sertoli cell-only, SCO). This phenotype can be caused by loss-of-function variants in the ion channel-encoding gene CLCN2. The aim of this project is to gain mechanistic insights into the role of CLC-2 channels in male infertility. To this end, molecular, cellular, and system functions will be analysed using human iPSC-derived cultures and genetically modified mice. Analyses will include electrophysiology, live-cell imaging as well as in silico modelling, shedding light on the role of ion channels in male infertility.
| Seebohm, Guiscard | Institut für Genetik von Herzerkrankungen (IfGH) |
| Seebohm, Guiscard | Institut für Genetik von Herzerkrankungen (IfGH) |