Differentiation of equine bone marrow derived mesenchymal stem cells increases the expression of immunogenic genes

Barrachina, L. (Universidad de Zaragoza) ; Remacha, A.R. (Universidad de Zaragoza) ; Romero, A. (Universidad de Zaragoza) ; Zaragoza, P. (Universidad de Zaragoza) ; Vázquez, F.J. (Universidad de Zaragoza) ; Rodellar, C. (Universidad de Zaragoza)
Differentiation of equine bone marrow derived mesenchymal stem cells increases the expression of immunogenic genes
Resumen: Mesenchymal stem cells (MSCs) are a promising treatment for equine musculoskeletal injuries because of their ability to regulate the inflammation and to differentiate into other cell types. Since interest in allogeneic therapy is rising, concerns about MSC immunogenicity need to be addressed. Differentiated MSCs from several species increase their expression of immunogenic molecules and induce alloresponses, but equine MSC immunogenic profile after differentiation has not been reported. Therefore, the aim of this study was to assess the gene expression of immunogenic markers in tri-lineage differentiated equine bone marrow derived MSCs (eBM-MSCs). For this purpose, eBM-MSCs (n = 4) were differentiated into osteoblasts, adipocytes and chondrocytes. Differentiation was confirmed by specific staining and gene expression of lineage-related markers. Subsequently, gene expression of MHC-I, MHC-II, CD40 and CD80 was analyzed in undifferentiated (control) and tri-lineage differentiated eBM-MSCs. Osteogenesis and adipogenesis, but not chondrogenesis, significantly upregulated MHC-I; MHC-II expression significantly increased in the three lineages, while CD40 and CD80 expression did not change. Despite this, MHC-I and MHC-II upregulation after differentiation might lead to increased immunogenicity and risk of allorecognition, either eBM-MSCs differentiate in vivo after administration or they are differentiated prior to administration, with potential negative consequences for effectiveness and safety of allogeneic therapy.
Idioma: Inglés
DOI: 10.1016/j.vetimm.2018.04.004
Año: 2018
Publicado en: VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY 200 (2018), 1-6
ISSN: 0165-2427

Factor impacto JCR: 1.846 (2018)
Categ. JCR: VETERINARY SCIENCES rank: 28 / 141 = 0.199 (2018) - Q1 - T1
Categ. JCR: IMMUNOLOGY rank: 130 / 157 = 0.828 (2018) - Q4 - T3

Factor impacto SCIMAGO: 0.749 - Veterinary (miscellaneous) (Q1) - Immunology (Q1)

Financiación: info:eu-repo/grantAgreement/ES/DGA/LAGENBIO-GROUP
Financiación: info:eu-repo/grantAgreement/ES/MINECO/AGL2011-28609
Tipo y forma: Article (PostPrint)
Área (Departamento): Área Genética (Dpto. Anatom.,Embri.Genét.Ani.)
Área (Departamento): Área Medicina y Cirugía Animal (Dpto. Patología Animal)

Exportado de SIDERAL (2024-01-04-11:01:33)


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