4.6 Article

Secretory Profile of Adipose-Tissue-Derived Mesenchymal Stem Cells from Cats with Calicivirus-Positive Severe Chronic Gingivostomatitis

Journal

VIRUSES-BASEL
Volume 14, Issue 6, Pages -

Publisher

MDPI
DOI: 10.3390/v14061146

Keywords

cats; mesenchymal stem cells; secretome; feline chronic gingivostomatitis; immunoassay; ultra-high-performance liquid chromatography high-resolution mass spectrometry (UHPLC-HRMS); bioinformatics

Categories

Funding

  1. Instituto de Salud Carlos III (Red TerCel) [RD16/0011/0022]
  2. Consejeria de Economia, Innovacion, Ciencia y Empleo, Junta de Andalucia [UMA18-FEDERJA-133]
  3. Centro de Investigacion Biomedica en Red en Bioingenieria, Biomateriales y Nanomedicina VI National R&D&I Plan 2008-2011
  4. Ministerio de Ciencia, Innovacion y Universidades [PEJ2018-004785-A]

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This study analyzed the proteomic profile of secretomes produced by feline adipose-tissue-derived MSCs (fAd-MSCs) from cats with feline chronic gingivostomatitis (FCGS) caused by feline calicivirus (FCV). It was found that fAd-MSCs from cats with FCGS showed an increased expression of pro-inflammatory cytokines and an altered proteomic profile. These findings provide insights into the roles of MSCs in FCGS and may contribute to the identification of specific biomarkers and therapeutic targets.
The feline calicivirus (FCV) causes infections in cats all over the world and seems to be related to a broad variety of clinical presentations, such as feline chronic gingivostomatitis (FCGS), a severe oral pathology in cats. Although its etiopathogeny is largely unknown, FCV infection is likely to be a main predisposing factor for developing this pathology. During recent years, new strategies for treating FCGS have been proposed, based on the use of mesenchymal stem cells (MSC) and their regenerative and immunomodulatory properties. The main mechanism of action of MSC seems to be paracrine, due to the secretion of many biomolecules with different biological functions (secretome). Currently, several pathologies in humans have been shown to be related to functional alterations of the patient's MSCs. However, the possible roles that altered MSCs might have in different diseases, including virus-mediated diseases, remain unknown. We have recently demonstrated that the exosomes produced by the adipose-tissue-derived MSCs (fAd-MSCs) from cats suffering from FCV-positive severe and refractory FCGS showed altered protein contents. Based on these findings, the goal of this work was to analyze the proteomic profile of the secretome produced by feline adipose-tissue-derived MSCs (fAd-MSCs) from FCV-positive patients with FCGS, in order to identify differences between them and to increase our knowledge of the etiopathogenesis of this disease. We used high-resolution mass spectrometry and functional enrichment analysis with Gene Ontology to compare the secretomes produced by the fAd-MSCs of healthy and calicivirus-positive FCGS cats. We found that the fAd-MSCs from cats with FCGS had an increased expression of pro-inflammatory cytokines and an altered proteomic profile compared to the secretome produced by cells from healthy cats. These findings help us gain insight on the roles of MSCs and their possible relation to FCGS, and may be useful for selecting specific biomarkers and for identifying new therapeutic targets.

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