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Detalle de: Mesenchymal stromal cells (MSC) from JAK2+myeloproliferative neoplasms differ from normal MSC and contribute to the maintenance of neoplastic hematopoiesis

Title Mesenchymal stromal cells (MSC) from JAK2+myeloproliferative neoplasms differ from normal MSC and contribute to the maintenance of neoplastic hematopoiesis
Abstract

There is evidence of continuous bidirectional cross-talk between malignant cells and bone marrow-derived mesenchymal stromal cells (BM-MSC), which favors the emergence and progression of myeloproliferative neoplastic (MPN) diseases. In the current work we have compared the function and gene expression profile of BM-MSC from healthy donors (HD-MSC) and patients with MPN (JAK2V617F), showing no differences in the morphology, proliferation and differentiation capacity between both groups. However, BM-MSC from MPN expressed higher mean fluorescence intensity (MIF) of CD73, CD44 and CD90, whereas CD105 was lower when compared to controls. Gene expression profile of BM-MSC showed a total of 169 genes that were differentially expressed in BM-MSC from MPN patients compared to HD-MSC. In addition, we studied the ability of BM-MSC to support the growth and survival of hematopoietic stem/progenitor cells (HSPC), showing a significant increase in the number of CFU-GM colonies when MPN-HSPC were co-cultured with MPN-MSC. Furthermore, MPN-MSC showed alteration in the expression of genes associated to the maintenance of hematopoiesis, with an overexpression of SPP1 and NF-kB, and a downregulation of ANGPT1 and THPO. Our results suggest that BM-MSC from JAK2+ patients differ from their normal counterparts and favor the maintenance of malignant clonal hematopoietic cells.

Apa Reference Ramos, T. L., Sánchez-Abarca, L. I., Rosón-Burgo, B., Redondo, A., Rico, A., Preciado, S., Ortega, R., Rodríguez, C., Muntión, S., Hernández-Hernández, Á., De Las Rivas, J., González, M., González Porras, J. R., del Cañizo, C., & Sánchez-Guijo, F. (2017). Mesenchymal stromal cells (MSC) from JAK2+ myeloproliferative neoplasms differ from normal MSC and contribute to the maintenance of neoplastic hematopoiesis. PLOS ONE, 12(8), e0182470. 10.1371/journal.pone.0182470
Doi 10.1371/journal.pone.0182470
Publication Date 10 Aug 2017
Publication Type Article
Researcher Javier De Las Rivas
Ontology Transcriptomics, Expression Profiling
Research Groups Bioinformatics and Functional Genomics
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