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The role of reactive oxygen species (ROS) in the signaling of FSH and ovarian factors

Subject Area Reproductive Medicine, Urology
Endocrinology, Diabetology, Metabolism
Term from 2014 to 2019
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 262625742
 
Final Report Year 2018

Final Report Abstract

1. We could not confirm initial pilot results, namely that FSH action in human granulosa cells (primary and KGN) involves elevations of ROS/H2O2 levels. This caused a reorientation of the project focusing more on H2O2 as signaling molecule. 2. We identified ROS/H2O2-generating enzymes, specifically NOX4, which produces H2O2. We partially identified and characterized the H2O2 system of the human follicle, including aquaporins as H2O2 transporters and linked H2O2 actions to beneficial consequences, mainly cell growth. 3. We explored GC-derived factors in the FF (PEDF, L-DOPA, DA). We described that PEDF has ROS-elevating actions, resulting in GC death. We identified antioxidant properties of L-DOPA, which contrast with ROS-­elevating actions of DA in human GCs. 4. Still ongoing studies will add to the mentioned antioxidant actions of L-DOPA in KGN and will furthermore delineate the consequences of FSH stimulation in primary GCs and KGN cells at the proteomic level. The data obtained during this project collectively highlight the importance of ROS and H2O2 in the human ovary and possibly GC tumors; results that may be of clinical relevance as well. The results also raised a series of new questions, which may in the near future result in a follow-up proposal.

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