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Light Sheet Microscopy and 3D Analysis of Human iPSC-derived Embryoid Bodies
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Embryoid bodies (EBs) are multicellular three-dimensional (3D) aggregates generated from induced pluripotent stem cells (iPSCs) in suspension and serve as useful biological sources for many downstream applications. Imaging of live EBs has been hampered mainly due to the inherent limitations of the imaging techniques applied to date. This study aimed to image human iPSC (hiPSC) derived EBs to obtain their 3D volume, determining size, morphology, and cell viability from day 7 to 14 using Light Sheet Fluorescence Microscopy (LSFM). Furthermore, chromosomal stability was assessed using Multicolor fluorescence in situ hybridization (M-FISH) from day 8 to 14. EB volume increased from day 7 to 13 which, decreased at day 14. From day 7 to 11, the EBs mainly appeared spherical and morphed into an ellipsoidal shape by day 13. All EBs showed varied external morphologies and larger cavities at day 14. The EB karyotype was diploid 46XY at day 8 and exhibited a low level of aneuploidy from day 10 to 14. This study shows that an increase in cell death affects the morphology and chromosomal stability in EBs derived from hiPSC. We demonstrate that the combination of LSFM and M-FISH helps characterize EBs that will assist future stem cell therapies.
Title: Light Sheet Microscopy and 3D Analysis of Human iPSC-derived Embryoid Bodies
Description:
Embryoid bodies (EBs) are multicellular three-dimensional (3D) aggregates generated from induced pluripotent stem cells (iPSCs) in suspension and serve as useful biological sources for many downstream applications.
Imaging of live EBs has been hampered mainly due to the inherent limitations of the imaging techniques applied to date.
This study aimed to image human iPSC (hiPSC) derived EBs to obtain their 3D volume, determining size, morphology, and cell viability from day 7 to 14 using Light Sheet Fluorescence Microscopy (LSFM).
Furthermore, chromosomal stability was assessed using Multicolor fluorescence in situ hybridization (M-FISH) from day 8 to 14.
EB volume increased from day 7 to 13 which, decreased at day 14.
From day 7 to 11, the EBs mainly appeared spherical and morphed into an ellipsoidal shape by day 13.
All EBs showed varied external morphologies and larger cavities at day 14.
The EB karyotype was diploid 46XY at day 8 and exhibited a low level of aneuploidy from day 10 to 14.
This study shows that an increase in cell death affects the morphology and chromosomal stability in EBs derived from hiPSC.
We demonstrate that the combination of LSFM and M-FISH helps characterize EBs that will assist future stem cell therapies.
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