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Hydrogen sulfide (H2S) as a regulator of redox homeostasis during glomerulonephritis (A07)

Subject Area Pharmacology
Term from 2009 to 2020
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 61867463
 
Various forms of inflammatory diseases are accompanied by a massive synthesis of redox-active mediators such as ROS, NO and H2S. We developed a method that allows the proteom-wide detection of hydropersulfides on cysteines as H2S-induced redox switches. The aim of this research project is to demonstrate the relevance of these thiol-based redox switches for glomerular nephropathies and cutaneous wound healing in suitable cell culture and animal models. The detailed knowledge of redox-modifications of cysteine residues as a concerted target of ROS, NO and H2S should help to elaborate therapeutic strategies for the treatment of inflammatory diseases.
DFG Programme Collaborative Research Centres
 
 

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