S-Nitrosylating Agents: A Novel Class of Compounds That Increase Cystic Fibrosis Transmembrane Conductance Regulator Expression and Maturation in Epithelial Cells

• DOI: 10.1124/mol.106.023242
• Publication Date: 2006-07-21T00:33:44Z
• Authors: Khalequz Zaman; Silvia Carraro; Joseph Doherty; Edward M. Henderson; Elizabeth Lendermon; Lei Liu; George Verghese; Molly Zigler; Mark Ross; Edward Park; Lisa A. Palmer; Allan Doctor; Jonathan S. Stamler; Benjamin Gaston
• Keywords: 0301 basic medicine; S-Nitrosothiols; Molecular Structure; Cystic Fibrosis Transmembrane Conductance Regulator; Membrane Proteins; Cell Differentiation; Epithelial Cells; HSP40 Heat-Shock Proteins; Endoplasmic Reticulum; Cell Line; 03 medical and health sciences; Gene Expression Regulation; S-Nitrosoglutathione; Humans; HSP70 Heat-Shock Proteins; Protein Processing, Post-Translational

The endogenous bronchodilator, S-nitrosoglutathione (GSNO), increases expression, maturation, and function of both the wild-type and the DeltaF508 mutant of the cystic fibrosis transmembrane conductance regulatory protein (CFTR). Though transcriptional mechanisms of action have been identified, GSNO seems also to have post-transcriptional effects on CFTR maturation. Here, we report that 1) GSNO is only one of a class of S-nitrosylating agents that, at low micromolar concentrations, increase DeltaF508 and wild-type CFTR expression and maturation; 2) NO itself (at these concentrations) and 8-bromocyclic GMP are minimally active on CFTR; 3) a novel agent, S-nitrosoglutathione diethyl ester, bypasses the need for GSNO bioactivation by gamma-glutamyl transpeptidase to increase CFTR maturation; 4) surprisingly, expression-but not S-nitrosylation-of cysteine string proteins (Csp) 1 and 2 is increased by GSNO; 5) the effect of GSNO to increase full maturation of wild-type CFTR is inhibited by Csp silencing (si)RNA; 6) proteins relevant to CFTR trafficking are SNO-modified, and SNO proteins traffic through the endoplasmic reticulum (ER) and Golgi after GSNO exposure; and 7) GSNO alters the interactions of DeltaF508 CFTR with Csp and Hsc70 in the ER and Golgi. These data suggest that GSNO is one of a class of S-nitrosylating agents that act independently of the classic NO radical/cyclic GMP pathway to increase CFTR expression and maturation. They also suggest that the effect of GSNO is dependent on Csp and on intracellular SNO trafficking. We speculate that these data will be of relevance to the development of NO donor-based therapies for CF.