Hydrogen Sulfide-Linked Sulfhydration of NF-kappa B Mediates Its Antiapoptotic Actions

Abstract

Nuclear factor kappa B (NF kappa B) is an antiapoptotic transcription factor. We show that the antiapoptotic actions of NF-kappa B are mediated by hydrogen sulfide (H(2)S) synthesized by cystathionine gamma-lyase (CSE). TNF-alpha treatment triples H(2)S generation by stimulating binding of SP1 to the CSE promoter. H(2)S generated by CSE stimulates DNA binding and gene activation of NF-kappa B, processes that are abolished in CSE-deleted mice. As CSE deletion leads to decreased glutathione levels, resultant oxidative stress may contribute to alterations in CSE mutant mice. H(2)S acts by sulfhydrating the p65 subunit of NF-kappa B at cysteine-38, which promotes its binding to the coactivator ribosomal protein S3 (RPS3). Sulfhydration of p65 predominates early after TNF-alpha treatment, then declines and is succeeded by a reciprocal enhancement of p65 nitrosylation. In CSE mutant mice, antiapoptotic influences of NF-kappa B are markedly diminished. Thus, sulfhydration of NF-kappa B appears to be a physiologic determinant of its antiapoptotic transcriptional activity.