Induction of neuroepithelial stem cells from mouse embryonic stem cells treated with retinoic acid.
Shunmei Chiba, Hiroaki Sekino, Noboru Suzuki
Abstract
Open-access reader
Shunmei Chiba, Hiroaki Sekino, Noboru Suzuki
Abstract
Open-access reader
Embryonic stem cells can be applicable for neural cell transplantation. Here we differentiated mouse embryonic stem cells into neuroepithelial stem cells with tertiary structures in floating cell aggregates. We first cultured ES cells with 0.5μM retinoic acid to induce neural differentiation. RT-PCR and immunostainning studies showed most of the RA treated cells at day 8 differentiated into Nestin expressing neural stem cells without tertiary structures. About 80% of the treated cells become panNCAM+ neural cells by FACS analysis. The findings indicated the RA treatment successfully induced neural stem cells from ES cells. The RA treated cells at day 8 were recovered and were cultured in FCS depleted medium consisted of DMEM/F 12, N 2 supplement and fibronectin on nontreated dishes for additional 6-8 days. The cell aggregates contained a cluster of pseudostratified Nestin+ neuroepithelial stem cells surrounded by the Masson staining+ basement membrane, whereas mature neural cells located outside of the structures. Thus, we have generated neuroepithelial stem cells from ES cells. These findings may get access to induce purposive and transplantable neurons for several diseases and get a cue to resolve inaccessible problems of neurogenesis.
OpenAlex reports 2 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Embryonic stem cells can be applicable for neural cell transplantation. Here we differentiated mouse embryonic stem cells into neuroepithelial stem cells with tertiary structures in floating cell aggregates. We first cultured ES cells with 0.5μM retinoic acid to induce neural differentiation. RT-PCR and immunostainning studies showed most of the RA treated cells at day 8 differentiated into Nestin expressing neural stem cells without tertiary structures. About 80% of the treated cells become panNCAM+ neural cells by FACS analysis. The findings indicated the RA treatment successfully induced neural stem cells from ES cells. The RA treated cells at day 8 were recovered and were cultured in FCS depleted medium consisted of DMEM/F 12, N 2 supplement and fibronectin on nontreated dishes for additional 6-8 days. The cell aggregates contained a cluster of pseudostratified Nestin+ neuroepithelial stem cells surrounded by the Masson staining+ basement membrane, whereas mature neural cells located outside of the structures. Thus, we have generated neuroepithelial stem cells from ES cells. These findings may get access to induce purposive and transplantable neurons for several diseases and get a cue to resolve inaccessible problems of neurogenesis.
Key concepts: Neuroepithelial cell, Stem cell, Neurosphere, Embryonic stem cell, Neural stem cell, Nestin, Cell biology, P19 cell