PR002230 (Project)

Description:Exfoliative toxins (ETs) are glutamyl endopeptidases (GEPs) of the chymotrypsin-like serine protease family (CLSPs) that play crucial roles in diverse skin diseases. Specifically, exfoliative toxin C (ExhC), expressed by Mammaliicoccus sciuri, is an atypical CLSP and is been classified as a moonlighting protein due to its ability to induce necrosis in specific cell lines, inhibits the phagocytic activity of macrophages, and causes skin exfoliation in pigs and mice. The latter function is due to the high specificity of ExhC for porcine and murine desmoglein-1, a cadherin that contributes to cell-cell adhesion within the epidermis. While the amino acid residues responsible for ExhC-induced necrosis have been identified, the specific cellular metabolic pathways it affects to induce cell death remain unclear. Herein, we employed Nuclear Magnetic Resonance (NMR) and Mass Spectrometry (MS) to explore the metabolic pathways affected by the necrotic activity of ExhC in the BHK-21 cell line. The metabolic profile of cells exposed to sub-toxic doses of ExhC revealed significant alterations in oxidative stress protection, energy production, and gene expression pathways. The data demonstrate the potential mechanisms of action of ExhC and highlight that this toxin causes cellular damage, even at low concentrations.