Direct isolation and RNA-seq reveal environment-dependent properties of engrafted neural stem/progenitor cells
Neural stem/progenitor cell (NSPC) transplantation is a promising treatment for various neurodegenerative disorders including spinal cord injury, however, no direct analysis has ever been performed on their in vivo profile after transplantation. Here we combined bioimaging, flow-cytometric isolation...
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Veröffentlicht in: | Nature communications 2012-10, Vol.3 (1), p.1140-1140, Article 1140 |
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Zusammenfassung: | Neural stem/progenitor cell (NSPC) transplantation is a promising treatment for various neurodegenerative disorders including spinal cord injury, however, no direct analysis has ever been performed on their
in vivo
profile after transplantation. Here we combined bioimaging, flow-cytometric isolation and ultra-high-throughput RNA sequencing to evaluate the cellular properties of engrafted NSPCs. The acutely transplanted NSPCs had beneficial effects on spinal cord injury, particularly neuroprotection and neurohumoral secretion, whereas their
in situ
secretory activity differed significantly from that predicted
in vitro
. The RNA-sequencing of engrafted NSPCs revealed dynamic expression/splicing changes in various genes involved in cellular functions and tumour development depending on graft environments. Notably, in the pathological environment, overall transcriptional activity, external signal transduction and neural differentiation of engrafted NSPCs were significantly suppressed. These results highlight the vulnerability of engrafted NSPCs to environmental force, while emphasizing the importance of
in situ
analysis in advancing the efficacy and safety of stem cell-based therapies.
Studies on neural stem and progenitor cells have shown they may be useful in treating spinal cord injuries, but the results are variable. Kumamaru
et al.
transplant these cells in injured spinal cords of mice, and find that their therapeutic properties are dynamically altered depending on their environment. |
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ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/ncomms2132 |