Top-Down Proteomics of Human Saliva Discloses Significant Variations of the Protein Profile in Patients with Mastocytosis.
Simone SerraoDavide FirinuAlessandra OlianasMargherita DeiddaCristina ContiniFederica IavaroneM Teresa SannaMozhgan BoroumandFrancisco AmadoMassimo CastagnolaIrene MessanaStefano Del GiaccoBarbara ManconiTiziana CabrasPublished in: Journal of proteome research (2020)
Mastocytosis is a myeloproliferative neoplasm causing abnormal clonal mast cell accumulation in different tissues, such as skin and bone marrow. A cutaneous subtype (CM) is distinguished from a systemic one (SM); SM patients can be grouped into SM with (SM+C) or without (SM-C) additional cutaneous lesions, and their classification is often challenging. This study was purposed to highlight variations in the salivary proteome of patients with different mastocytosis subtypes and compared to healthy controls. A top-down proteomics approach coupled to a label-free quantitation revealed salivary profiles in patients different from those of controls and a down-regulation of peptides/proteins involved in the mouth homeostasis and defense, such as statherin, histatins, and acidic proline-rich proteins (aPRPs), and in innate immunity and inflammation, such as the cathepsin inhibitors, suggesting a systemic condition associated with an exacerbated inflammatory state. The up-regulation of antileukoproteinase and S100A8 suggested a protective role against the disease status. The two SM forms were distinguished by the lower levels of truncated forms of aPRPs, statherin, P-B peptide, and cystatin D and the higher levels of thymosin β4 and α-defensins 1 and 4 in SM-C patients with respect to SM+C. Data are available via ProteomeXchange with identifier PXD017759.
Keyphrases
- end stage renal disease
- label free
- bone marrow
- mass spectrometry
- chronic kidney disease
- ejection fraction
- newly diagnosed
- oxidative stress
- prognostic factors
- endothelial cells
- gene expression
- single cell
- electronic health record
- deep learning
- patient reported outcomes
- liquid chromatography tandem mass spectrometry
- high resolution
- soft tissue