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Insights into the human mesenchymal stromal/stem cell identity through integrative transcriptomic profiling.
Roson-Burgo, Beatriz; Sanchez-Guijo, Fermin; Del Cañizo, Consuelo; De Las Rivas, Javier.
Afiliación
  • Roson-Burgo B; Bioinformatics and Functional Genomics Group, Cancer Research Center (IBMCC, CSIC/USAL) and IBSAL, Consejo Superior de Investigaciones Cientificas (CSIC), Salamanca, Spain.
  • Sanchez-Guijo F; Hematology Department, IBSAL-Hospital Universitario de Salamanca, Salamanca, Spain.
  • Del Cañizo C; Centro en Red de Medicina Regenerativa y Terapia Celular de Castilla y León, Salamanca, Spain.
  • De Las Rivas J; Hematology Department, IBSAL-Hospital Universitario de Salamanca, Salamanca, Spain.
BMC Genomics ; 17(1): 944, 2016 Nov 21.
Article en En | MEDLINE | ID: mdl-27871224
BACKGROUND: Mesenchymal Stromal/Stem Cells (MSCs), isolated under the criteria established by the ISCT, still have a poorly characterized phenotype that is difficult to distinguish from similar cell populations. Although the field of transcriptomics and functional genomics has quickly grown in the last decade, a deep comparative analysis of human MSCs expression profiles in a meaningful cellular context has not been yet performed. There is also a need to find a well-defined MSCs gene-signature because many recent biomedical studies show that key cellular interaction processes (i.e. inmuno-modulation, cellular cross-talk, cellular maintenance, differentiation, epithelial-mesenchymal transition) are dependent on the mesenchymal stem cells within the stromal niche. RESULTS: In this work we define a core mesenchymal lineage signature of 489 genes based on a deep comparative analysis of multiple transcriptomic expression data series that comprise: (i) MSCs of different tissue origins; (ii) MSCs in different states of commitment; (iii) other related non-mesenchymal human cell types. The work integrates several public datasets, as well as de-novo produced microarray and RNA-Seq datasets. The results present tissue-specific signatures for adipose tissue, chorionic placenta, and bone marrow MSCs, as well as for dermal fibroblasts; providing a better definition of the relationship between fibroblasts and MSCs. Finally, novel CD marker patterns and cytokine-receptor profiles are unravelled, especially for BM-MSCs; with MCAM (CD146) revealed as a prevalent marker in this subtype of MSCs. CONCLUSIONS: The improved biomolecular characterization and the released genome-wide expression signatures of human MSCs provide a comprehensive new resource that can drive further functional studies and redesigned cell therapy applications.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Madre Mesenquimatosas / Transcriptoma Límite: Female / Humans / Pregnancy Idioma: En Revista: BMC Genomics Asunto de la revista: GENETICA Año: 2016 Tipo del documento: Article País de afiliación: España Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Madre Mesenquimatosas / Transcriptoma Límite: Female / Humans / Pregnancy Idioma: En Revista: BMC Genomics Asunto de la revista: GENETICA Año: 2016 Tipo del documento: Article País de afiliación: España Pais de publicación: Reino Unido