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| Título: | Supplementary Information for Binucleated human bone marrow-derived mesenchymal cells can be formed during neural-like differentiation with independence of any cell fusion events |
Autor: | Bueno, Carlos Roberto CSIC ORCID; Blanquer, Miguel; García-Bernal, David CSIC ORCID; Martínez, Salvador CSIC ORCID; Moraleda, José María | Fecha de publicación: | 2022 | Editor: | Springer Nature | Citación: | Bueno, Carlos Roberto; Blanquer, Miguel; García-Bernal, David; Martínez, Salvador; Moraleda, José María; 2022; Supplementary Information for Binucleated human bone marrow-derived mesenchymal cells can be formed during neural-like differentiation with independence of any cell fusion events [Dataset]; Springer Nature; https://doi.org/10.1038/s41598-022-24996-8 | Descripción: | Supplementary Figures: Figure S1. Morphology and immunophenotypes of hBM-MSCs. Figure S2. The mayority of hBM-MSCs assumed a spherical morphology within 12 hours of exposure to neural induction media. Figure S3. Morphological changes in hBM-MSC-derived intermediate cells. Figure S4. hBM-MSC-derived neural-like cells create connections via extensions of their neurites. Figure S5. Intermediate hBM-MSC nuclei can switch their morphology and positioning. Figure S6. Nuclear morphology and positioning during neuronal-like polarisation of hBM-MSC-derived intermediate cells. Figure S7. Nuclear morphology when hBM-MSC-derived intermediate cells redifferentiate back to the mesenchymal fate. Figure S8. hBM-MSCs exhibit unusual nuclear structures and chromatin-containing bodies in the cellular cytoplasm during neural-like differentiation. | URI: | http://hdl.handle.net/10261/312321 | DOI: | 10.1038/s41598-022-24996-8 | Referencias: | Bueno, Carlos Roberto; Blanquer, Miguel; García-Bernal, David; Martínez, Salvador; Moraleda, José María. Binucleated human bone marrow-derived mesenchymal cells can be formed during neural-like differentiation with independence of any cell fusion events. https://doi.org/10.1038/s41598-022-24996-8.http://hdl.handle.net/10261/306712 |
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