Traditional
differentiation protocols use embryoid body (EB) formation as the first
step of lineage restriction to mimic early human embryogenesis, which
is then followed by manual selection of neuroepithelial precursors. This
procedure is tedious and often inconsistent. We have developed a novel
neural differentiation scheme that directs human iPSCs (created with the
Allele 6F mRNA reprogramming kit)
that progressed, as attached culture, to neural precursor cells (NPCs)
in just 4-6 days, half the time it typically takes by other methods.
From NPCs it takes about another 5-6 days for neural rosettes to form
(see figures below); upon passage, cells in neural rosettes
differentiate into neurons in 24 hours.
The
neural progenitors at the rosettes stage can be stocked and expanded,
before differentiated into different types of neurons. We are working on
specifically and efficiently different these neural progenitor cells
into dopaminergic, glutamatergic, GABAergic, and other types of
sub-types of neurons with Allele’s technologies (Questions? email the
Allele Stem Cell Group at iPSatAllelebiotech.com).
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