par Najar, Mehdi 
;Dollé, Laurent;Crompot, Emerence ;Verhulst, Stefaan;van Grunsven, L.A.;Busser, Hélène ;Lagneaux, Laurence
Référence Tissue Engineering. Part C. Methods, 24, 2, page (89-98)
Publication Publié, 2018-02
;Dollé, Laurent;Crompot, Emerence ;Verhulst, Stefaan;van Grunsven, L.A.;Busser, Hélène ;Lagneaux, Laurence Référence Tissue Engineering. Part C. Methods, 24, 2, page (89-98)
Publication Publié, 2018-02
Article révisé par les pairs
| Résumé : | Mesenchymal stromal cells (MSCs) have particular properties that allow their use as therapeutic strategies for several cell-based applications. Historically, bone marrow (BM)-MSCs are isolated by culture adherence since specific cell surface markers are yet to be developed. This original work aimed to identify and characterize isolating expanded BM-MSCs based on their aldehyde dehydrogenase (ALDH) activity known to be a hallmark of stem cells and relevant for their isolation. We thus isolated by fluorescence-activated cell sorting technology two functionally different populations of BM-MSCs depending on their ALDH activity (ALDH+ and ALDH-). Transcriptome analysis and profiling clearly demonstrated that both populations of BM-MSCs present distinct pattern of genes related to the main properties of MSCs (proliferation, response to hypoxia, angiogenesis, phenotype, stemness, multilineage, hematopoiesis, immunomodulation) in an ALDH activity dependent manner. Both BM-MSC populations look to significantly differ in terms of biological responses and functionalities. More functional analyses are needed to understand and characterize the properties of these ALDH populations. Collectively, our results highlight ALDH activity as a potential feature for isolating and segregating functional and/or competent subset of BM-MSC populations, which may account for better and more efficient therapeutic issue. |
